The bone marrow niche for haematopoietic stem cells
Open accessAbstract
Niches are local tissue microenvironments that maintain and regulate stem cells. Haematopoiesis provides a model for understanding mammalian stem cells and their niches, but the haematopoietic stem cell (HSC) niche remains incompletely defined and beset by competing models. Recent progress has been made in elucidating the location and cellular components of the HSC niche in the bone marrow. The niche is perivascular, created partly by mesenchymal stromal cells and endothelial cells and often, but not always, located near trabecular bone. Outstanding questions concern the cellular complexity of the niche, the role of the endosteum and functional heterogeneity among perivascular microenvironments.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Non-haematopoietic stromal cells, including osteoblasts and osteoprogenitor cells, promote the maintenance of haematopoietic stem cells.
“Non-haematopoietic stromal cells, including osteoblasts and osteoprogenitor cells, promote the maintenance of haematopoietic stem cells.95”
From The costs and benefits of senotherapeutics for human health (2022) · cites this paper as [95]
Other cell types that regulate HSC niches include osteoclasts, extracellular matrix, megakaryocytes, and calcium.
“Other cell types that regulate HSC niches include osteoclasts, extracellular matrix, megakaryocytes, and calcium.9”
From Inflammatory bone marrow microenvironment (2019) · cites this paper as [9]
Perivascular mesenchymal cells that express CD146 in humans and Cxcl12-GFP, Nestin-GFP, full-length Leptin receptor, Prx-1-Cre, Osterix-Cre, and inducible Mx-1-Cre in mice generate osteoblastic cells and express factors that promote the maintenance of HSPCs.
“Although MSCs are a heterogeneous population and still require better characterization by surface markers, perivascular mesenchymal cells that express CD146 in humans and Cxcl12-green fluorescent protein, Nestin-green fluorescent protein, full-length Leptin receptor, Prx-1-Cre, Osterix-Cre, and inducible Mx-1-Cre in mice generate osteoblastic cells and express factors that promote the maintenance”
From Inflammatory bone marrow microenvironment (2019) · cites this paper as [9]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients
Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,834 · see citing works
Cytokine-mediated regulation of CXCR4 expression in human neutrophils
Nagase, H., Miyamasu, M., Yamaguchi, M., Imanishi, M., Tsuno, N. H., Matsushima, K., Yamamoto, K., Morita, Y., & Hirai, K. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.4.711 · Cited by 4,713 · see citing works
A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells1
Till, J. E., & McCulloch, E. A. (2010) · Radiation Research · doi:10.1667/rrxx28.1 · Cited by 4,036 · see citing works
A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells
Till, J. E., & McCulloch, E. A. (1961) · Radiation Research · doi:10.2307/3570892 · Cited by 3,770 · see citing works
Osteoblastic cells regulate the haematopoietic stem cell niche
Calvi, L. M., Adams, G. B., Weibrecht, K. W., Weber, J. M., Olson, D. P., Knight, M. C., Martin, R. P., Schipani, E., Pajevic, P. D., Bringhurst, F. R., et al. (2003) · Nature · doi:10.1038/nature02040 · Cited by 3,452 · see citing works
Self-citationMesenchymal and haematopoietic stem cells form a unique bone marrow niche
Méndez‐Ferrer, S., Michurina, T. V., Ferraro, F., Mazloom, A. R., MacArthur, B. D., Lira, S. A., Scadden, D. T., Ma’ayan, A., Enikolopov, G., & Frenette, P. S. (2010) · Nature · doi:10.1038/nature09262 · Cited by 3,381 · see citing works
Self-citationKiel, M. J., Yilmaz, Ö. H., Iwashita, T., Yilmaz, O. H., Terhorst, C., & Morrison, S. J. (2005) · Cell · doi:10.1016/j.cell.2005.05.026 · Cited by 3,168 · see citing works
Self-citationIdentification of the haematopoietic stem cell niche and control of the niche size
Zhang, J., Niu, C. S., Ye, L., Huang, H., He, X. C., Tong, W.-G., Ross, J., Haug, J., Johnson, T. J., Feng, J. Q., et al. (2003) · Nature · doi:10.1038/nature02041 · Cited by 2,948 · see citing works
Purification and Characterization of Mouse Hematopoietic Stem Cells
Spangrude, G. J., Heimfeld, S., & Weissman, I. L. (1988) · Science · doi:10.1126/science.2898810 · Cited by 2,889 · see citing works
Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development
Zou, Y.-R., Kottmann, A. H., Kuroda, M., Taniuchi, I., & Littman, D. R. (1998) · Nature · doi:10.1038/31269 · Cited by 2,494 · see citing works
Sugiyama, T., Kohara, H., Noda, M., & Nagasawa, T. (2006) · Immunity · doi:10.1016/j.immuni.2006.10.016 · Cited by 2,419 · see citing works
Nagasawa, T., Hirota, S., Tachibana, K., Takakura, N., Nishikawa, S.-I., Kitamura, Y., Yoshida, N., Kikutani, H., & Kishimoto, T. (1996) · Nature · doi:10.1038/382635a0 · Cited by 2,338 · see citing works
The relationship between the spleen colony-forming cell and the haemopoietic stem cell.
Schofield, R. (1978) · PubMed · Cited by 2,319 · see citing works
Sacchetti, B., Funari, A., Michienzi, S., Di Cesare, S., Piersanti, S., Saggio, I., Tagliafico, E., Ferrari, S., Robey, P. G., Riminucci, M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.08.025 · Cited by 2,226 · see citing works
Conditions controlling the proliferation of haemopoietic stem cells in vitro
Dexter, T. M., Allen, T., & Lajtha, L. G. (1977) · Journal of Cellular Physiology · doi:10.1002/jcp.1040910303 · Cited by 2,120 · see citing works
Haeckel, E. (1866) · De Gruyter eBooks · doi:10.1515/9783110848281 · Cited by 2,068 · see citing works
Tie2/Angiopoietin-1 Signaling Regulates Hematopoietic Stem Cell Quiescence in the Bone Marrow Niche
Arai, F., Hirao, A., Ohmura, M., Sato, H., Matsuoka, S., Takubo, K., Ito, K., Koh, G. Y., & Suda, T. (2004) · Cell · doi:10.1016/j.cell.2004.07.004 · Cited by 1,958 · see citing works
Stem Cells and Niches: Mechanisms That Promote Stem Cell Maintenance throughout Life
Morrison, S. J., & Spradling, A. C. (2008) · Cell · doi:10.1016/j.cell.2008.01.038 · Cited by 1,951 · see citing works
Self-citationEndothelial and perivascular cells maintain haematopoietic stem cells
Ding, L., Saunders, T. L., Enikolopov, G., & Morrison, S. J. (2012) · Nature · doi:10.1038/nature10783 · Cited by 1,934 · see citing works
Self-citationWilson, A., Laurenti, E., Oser, G., van der Wath, R. C., Blanco-Bose, W., Jaworski, M., Offner, S., Dunant, C. F., Eshkind, L., Bockamp, E., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.048 · Cited by 1,908 · see citing works
The stem-cell niche as an entity of action
Scadden, D. T. (2006) · Nature · doi:10.1038/nature04957 · Cited by 1,859 · see citing works
Self-citationHeissig, B., Hattori, K., Dias, S., Friedrich, M., Ferris, B., Hackett, N. R., Crystal, R. G., Besmer, P., Lyden, D. C., Moore, M. A. S., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)00754-7 · Cited by 1,744 · see citing works
A Stem Cell Molecular Signature
Ivanova, N. B., Dimos, J. T., Schaniel, C., Hackney, J. A., Moore, K. A., & Lemischka, I. R. (2002) · Science · doi:10.1126/science.1073823 · Cited by 1,543 · see citing works
Signals from the Sympathetic Nervous System Regulate Hematopoietic Stem Cell Egress from Bone Marrow
Katayama, Y., Battista, M., Kao, W.-M., Hidalgo, A., Peired, A. J., Thomas, S. A., & Frenette, P. S. (2006) · Cell · doi:10.1016/j.cell.2005.10.041 · Cited by 1,412 · see citing works
CXCL12 in early mesenchymal progenitors is required for haematopoietic stem-cell maintenance
Greenbaum, A. M., Hsu, Y.-M. S., Day, R. B., Schuettpelz, L. G., Christopher, M. J., Borgerding, J. N., Nagasawa, T., & Link, D. C. (2013) · Nature · doi:10.1038/nature11926 · Cited by 1,372 · see citing works
G-CSF induces stem cell mobilization by decreasing bone marrow SDF-1 and up-regulating CXCR4
Petit, I., Szyper‐Kravitz, M., Nagler, A., Lahav, M., Peled, A., Habler, L., Ponomaryov, T., Taichman, R. S., Arenzana‐Seisdedos, F., Fujii, N., et al. (2002) · Nature Immunology · doi:10.1038/ni813 · Cited by 1,331 · see citing works
Haematopoietic stem cell release is regulated by circadian oscillations
Méndez‐Ferrer, S., Lucas, D., Battista, M., & Frenette, P. S. (2008) · Nature · doi:10.1038/nature06685 · Cited by 1,310 · see citing works
Haematopoietic stem cells and early lymphoid progenitors occupy distinct bone marrow niches
Ding, L., & Morrison, S. J. (2013) · Nature · doi:10.1038/nature11885 · Cited by 1,285 · see citing works
Self-citationArteriolar niches maintain haematopoietic stem cell quiescence
Kunisaki, Y., Bruns, I., Scheiermann, C., Ahmed, J. U., Pinho, S., Zhang, D., Mizoguchi, T., Wei, Q., Lucas, D., Ito, K., et al. (2013) · Nature · doi:10.1038/nature12612 · Cited by 1,236 · see citing works
Direct measurement of local oxygen concentration in the bone marrow of live animals
Spencer, J. A., Ferraro, F., Roussakis, E., Klein, A., Wu, J., Runnels, J. M., Zaher, W., Mortensen, L. J., Alt, C., Turcotte, R., et al. (2014) · Nature · doi:10.1038/nature13034 · Cited by 1,167 · see citing works
Self-citationBone progenitor dysfunction induces myelodysplasia and secondary leukaemia
Raaijmakers, M. H. G. P., Mukherjee, S., Guo, S., Zhang, S., Kobayashi, T., Schoonmaker, J. A., Ebert, B. L., Al-Shahrour, F., Hasserjian, R. P., Scadden, E. O., et al. (2010) · Nature · doi:10.1038/nature08851 · Cited by 1,115 · see citing works
Self-citationHereditary Anemias of the Mouse: A Review for Geneticists
Russell, E. S. (1979) · Advances in genetics · doi:10.1016/s0065-2660(08)60549-0 · Cited by 1,083 · see citing works
Physiological Migration of Hematopoietic Stem and Progenitor Cells
Wright, D. E., Wagers, A. J., Gulati, A. P., Johnson, F. L., & Weissman, I. L. (2001) · Science · doi:10.1126/science.1064081 · Cited by 933 · see citing works
Live-animal tracking of individual haematopoietic stem/progenitor cells in their niche
Celso, C. L., Fleming, H. E., Wu, J. W., Zhao, C. X., Miake-Lye, S., Fujisaki, J., Côté, D. C., Rowe, D. W., Lin, C. P., & Scadden, D. T. (2008) · Nature · doi:10.1038/nature07434 · Cited by 917 · see citing works
Self-citationThe distribution of colony‐forming cells among spleen colonies
Siminovitch, L., McCulloch, E. A., & Till, J. E. (1963) · Journal of Cellular and Comparative Physiology · doi:10.1002/jcp.1030620313 · Cited by 915 · see citing works
Regulation of the HIF-1α Level Is Essential for Hematopoietic Stem Cells
Takubo, K., Goda, N., Yamada, W., Iriuchishima, H., Ikeda, E., Kubota, Y., Shima, H., Johnson, R. S., Hirao, A., Suematsu, M., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.06.020 · Cited by 891 · see citing works
In vivo imaging of specialized bone marrow endothelial microdomains for tumour engraftment
Sipkins, D. A., Wei, X., Wu, J. W., Runnels, J. M., Côté, D. C., Means, T. K., Luster, A. D., Scadden, D. T., & Lin, C. P. (2005) · Nature · doi:10.1038/nature03703 · Cited by 880 · see citing works
Self-citationDistribution of hematopoietic stem cells in the bone marrow according to regional hypoxia
Parmar, K., Mauch, P., Vergilio, J.-A., Sackstein, R., & Down, J. D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701152104 · Cited by 867 · see citing works
Chow, A. T., Lucas, D., Hidalgo, A., Méndez‐Ferrer, S., Hashimoto, D., Scheiermann, C., Battista, M., Leboeuf, M., Prophete, C., van Rooijen, N., et al. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20101688 · Cited by 866 · see citing works
Stem Cell Factor and Hematopoiesis
Broudy, V. C. (1997) · Blood · doi:10.1182/blood.v90.4.1345 · Cited by 862 · see citing works
Omatsu, Y., Sugiyama, T., Kohara, H., Kondoh, G., Fujii, N., Kohno, K., & Nagasawa, T. (2010) · Immunity · doi:10.1016/j.immuni.2010.08.017 · Cited by 849 · see citing works
Morikawa, S., Mabuchi, Y., Kubota, Y., Nagai, Y., Niibe, K., Hiratsu, E., Suzuki, S., Miyauchi-Hara, C., Nagoshi, N., Sunabori, T., et al. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091046 · Cited by 833 · see citing works
c-Myc controls the balance between hematopoietic stem cell self-renewal and differentiation
Wilson, A., Murphy, M. J., Oskarsson, T., Kaloulis, K., Bettess, M. D., Oser, G. M., Pasche, A.-C., Knabenhans, C., MacDonald, H. R., & Trumpp, A. (2004) · Genes & Development · doi:10.1101/gad.313104 · Cited by 823 · see citing works
Molecular cloning and structure of a pre-B-cell growth-stimulating factor.
Nagasawa, T., Kikutani, H., & Kishimoto, T. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.6.2305 · Cited by 817 · see citing works
Yoshihara, H., Arai, F., Hosokawa, K., Hagiwara, T., Takubo, K., Nakamura, Y., Gomei, Y., Iwasaki, H., Matsuoka, S., Miyamoto, K., et al. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.10.020 · Cited by 816 · see citing works
Nilsson, S. K., Johnston, H. M., Whitty, G. A., Williams, B., Webb, R. J., Denhardt, D. T., Bertoncello, I., Bendall, L. J., Simmons, P. J., & Haylock, D. N. (2005) · Blood · doi:10.1182/blood-2004-11-4422 · Cited by 807 · see citing works
Hematopoiesis is severely altered in mice with an induced osteoblast deficiency
Višnjić, D., Kalajzić, Ž., Rowe, D. W., Katavić, V., Lorenzo, J., & Aguila, H. L. (2004) · Blood · doi:10.1182/blood-2003-11-4011 · Cited by 804 · see citing works
Winkler, I. G., Sims, N. A., Pettit, A. R., Barbier, V., Nowlan, B., Helwani, F., Poulton, I. J., van Rooijen, N., Alexander, K. A., Raggatt, L. J., et al. (2010) · Blood · doi:10.1182/blood-2009-11-253534 · Cited by 801 · see citing works
Nonmyelinating Schwann Cells Maintain Hematopoietic Stem Cell Hibernation in the Bone Marrow Niche
Yamazaki, S., Ema, H., Karlsson, G., Yamaguchi, T., Miyoshi, H., Shioda, S., Taketo, M. M., Karlsson, S., Iwama, A., & Nakauchi, H. (2011) · Cell · doi:10.1016/j.cell.2011.09.053 · Cited by 797 · see citing works
Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor
Adams, G. B., Chabner, K. T., Alley, I. R., Olson, D. P., Szczepiorkowski, Z. M., Poznansky, M. C., Kos, C. H., Pollak, M. R., Brown, E. M., & Scadden, D. T. (2005) · Nature · doi:10.1038/nature04247 · Cited by 782 · see citing works
Self-citationOsteoclasts degrade endosteal components and promote mobilization of hematopoietic progenitor cells
Kollet, Ó., Dar, A., Shivtiel, S., Kalinkovich, A., Lapid, K., Sztainberg, Y., Tesio, M., Samstein, R. M., Goichberg, P., Spiegel, A., et al. (2006) · Nature Medicine · doi:10.1038/nm1417 · Cited by 774 · see citing works
Rhythmic Modulation of the Hematopoietic Niche through Neutrophil Clearance
Casanova-Acebes, M., Pitaval, C., Weiss, L. A., Nombela‐Arrieta, C., Chèvre, R., A-González, N., Kunisaki, Y., Zhang, D., van Rooijen, N., Silberstein, L. E., et al. (2013) · Cell · doi:10.1016/j.cell.2013.04.040 · Cited by 752 · see citing works
Expression and function of c-kit in hemopoietic progenitor cells.
Ogawa, M., Matsuzaki, Y., Nishikawa, S., Hayashi, S., Kunisada, T., Sudo, T., Kina, T., Nakauchi, H., & Nishikawa, S. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.174.1.63 · Cited by 744 · see citing works
Stier, S., Ko, Y., Forkert, R., Lutz, C., Neuhaus, T., Grünewald, E., Cheng, T., Dombkowski, D., Calvi, L., Rittling, S., et al. (2005) · Journal of Experimental Medicine · doi:10.1084/jem.20041992 · Cited by 710 · see citing works
Self-citationButler, J. M., Nolan, D. J., Vertes, E. L., Varnum‐Finney, B., Kobayashi, H., Hooper, A. T., Seandel, M., Shido, K., White, I. A., Kobayashi, M., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.02.001 · Cited by 688 · see citing works
Oguro, H., Ding, L., & Morrison, S. J. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.05.014 · Cited by 657 · see citing works
Self-citationHooper, A. T., Butler, J. M., Nolan, D. J., Kranz, A., Iida, K., Kobayashi, M., Kopp, H., Shido, K., Petit, I., Yanger, K., et al. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.01.006 · Cited by 641 · see citing works
Park, D., Spencer, J. A., Koh, B. I., Kobayashi, T., Fujisaki, J., Clemens, T. L., Lin, C. P., Kronenberg, H. M., & Scadden, D. T. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.02.003 · Cited by 627 · see citing works
Self-citationSchepers, K., Pietras, E. M., Reynaud, D., Flach, J., Binnewies, M., Garg, T., Wagers, A. J., Hsiao, E. C., & Passegué, E. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.06.009 · Cited by 614 · see citing works
Uncertainty in the niches that maintain haematopoietic stem cells
Kiel, M. J., & Morrison, S. J. (2008) · Nature reviews. Immunology · doi:10.1038/nri2279 · Cited by 587 · see citing works
Self-citationAnalysis of histone 2B-GFP retention reveals slowly cycling hematopoietic stem cells
Foudi, A., Hochedlinger, K., Van Buren, D., Schindler, J. W., Jaenisch, R., Carey, V., & Hock, H. (2009) · Nature Biotechnology · doi:10.1038/nbt.1517 · Cited by 586 · see citing works
Ponomaryov, T., Peled, A., Petit, I., Taichman, R. S., Habler, L., Sandbank, J., Arenzana‐Seisdedos, F., Magérus, A., Carúz, A., Fujii, N., et al. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10329 · Cited by 584 · see citing works
The journey of developing hematopoietic stem cells
Mikkola, H. K. A., & Orkin, S. H. (2006) · Development · doi:10.1242/dev.02568 · Cited by 577 · see citing works
Critical Role of Thrombopoietin in Maintaining Adult Quiescent Hematopoietic Stem Cells
Qian, H., Buza-Vidas, N., Hyland, C. D., Jensen, C. T., Antonchuk, J., Månsson, R., Thorén, L., Ekblom, M., Alexander, W. S., & Jacobsen, S. E. W. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.10.008 · Cited by 563 · see citing works
Detection of functional haematopoietic stem cell niche using real-time imaging
Xie, Y., Yin, T., Wiegraebe, W., He, X., Miller, D., Stark, D. A., Perko, K., Alexander, R. L., Schwartz, J. W., Grindley, J. C., et al. (2008) · Nature · doi:10.1038/nature07639 · Cited by 554 · see citing works
Nombela‐Arrieta, C., Pivarnik, G., Winkel, B., Canty, K. J., Harley, B. A. C., Mahoney, J. E., Park, S., Lu, J., Protopopov, A. I., & Silberstein, L. E. (2013) · Nature Cell Biology · doi:10.1038/ncb2730 · Cited by 543 · see citing works
A Microenvironment-Induced Myeloproliferative Syndrome Caused by Retinoic Acid Receptor γ Deficiency
Walkley, C. R., Olsen, G. H., Dworkin, S., Fabb, S. A., Swann, J. B., McArthur, G. A., Westmoreland, S. V., Chambon, P., Scadden, D. T., & Purton, L. E. (2007) · Cell · doi:10.1016/j.cell.2007.05.014 · Cited by 535 · see citing works
Self-citationPinho, S., Lacombe, J., Hanoun, M., Mizoguchi, T., Bruns, I., Kunisaki, Y., & Frenette, P. S. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122252 · Cited by 504 · see citing works
Fleming, H. E., Janzen, V., Celso, C. L., Guo, J., Leahy, K. M., Kronenberg, H. M., & Scadden, D. T. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.01.003 · Cited by 500 · see citing works
Self-citationTran, E., Chinnasamy, D., Yu, Z., Morgan, R. A., Lee, C. R., Restifo, N. P., & Rosenberg, S. A. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20130110 · Cited by 467 · see citing works
Heterogeneity and hierarchy within the most primitive hematopoietic stem cell compartment
Morita, Y., Ema, H., & Nakauchi, H. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20091318 · Cited by 456 · see citing works
Winkler, I. G., Barbier, V., Nowlan, B., Jacobsen, R. N., Forristal, C. E., Patton, J. T., Magnani, J. L., & Lévesque, J.-P. (2012) · Nature Medicine · doi:10.1038/nm.2969 · Cited by 439 · see citing works
CD169 + macrophages provide a niche promoting erythropoiesis under homeostasis and stress
Chow, A., Huggins, M., Ahmed, J., Hashimoto, D., Lucas, D., Kunisaki, Y., Pinho, S., Leboeuf, M., Noizat, C., van Rooijen, N., et al. (2013) · Nature Medicine · doi:10.1038/nm.3057 · Cited by 433 · see citing works
Efficient Transplantation via Antibody-Based Clearance of Hematopoietic Stem Cell Niches
Czechowicz, A. D., Kraft, D. L., Weissman, I. L., & Bhattacharya, D. (2007) · Science · doi:10.1126/science.1149726 · Cited by 432 · see citing works
Endochondral ossification is required for haematopoietic stem-cell niche formation
Chan, C. K. F., Chen, C., Luppen, C. A., Kim, J., DeBoer, A., Wei, K., Helms, J. A., Kuo, C. J., Kraft, D. L., & Weissman, I. L. (2008) · Nature · doi:10.1038/nature07547 · Cited by 430 · see citing works
Rb Regulates Interactions between Hematopoietic Stem Cells and Their Bone Marrow Microenvironment
Walkley, C. R., Shea, J. M., Sims, N. A., Purton, L. E., & Orkin, S. H. (2007) · Cell · doi:10.1016/j.cell.2007.03.055 · Cited by 424 · see citing works
Roberts, E. W., Deonarine, A., Jones, J. O., Denton, A. E., Feig, C., Lyons, S. K., Espéli, M., Kraman, M., McKenna, B., Wells, R. J. B., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122344 · Cited by 417 · see citing works
Haematopoietic stem cells do not asymmetrically segregate chromosomes or retain BrdU
Kiel, M. J., He, S., Ashkenazi, R., Gentry, S. N., Teta, M., Kushner, J. A., Jackson, T. L., & Morrison, S. J. (2007) · Nature · doi:10.1038/nature06115 · Cited by 417 · see citing works
Self-citationTaichman, R. S., & Emerson, S. G. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.5.1677 · Cited by 414 · see citing works
CXCR4 is required for the quiescence of primitive hematopoietic cells
Nie, Y., Han, Y.-C., & Zou, Y.-R. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072513 · Cited by 407 · see citing works
Osteoblasts support B-lymphocyte commitment and differentiation from hematopoietic stem cells
Zhu, J., Garrett, R. W., Jung, Y., Zhang, Y., Kim, N., Wang, J., Joe, G. J., Hexner, E. O., Choi, Y., Taichman, R. S., et al. (2007) · Blood · doi:10.1182/blood-2006-08-041384 · Cited by 402 · see citing works
Kobayashi, H., Butler, J. M., O’Donnell, R. K., Kobayashi, M., Ding, B., Bonner, B., Chiu, V. K., Nolan, D. J., Shido, K., Benjamin, L. E., et al. (2010) · Nature Cell Biology · doi:10.1038/ncb2108 · Cited by 402 · see citing works
Hematopoietic stem cell deficiencies in mice lacking c-Mpl, the receptor for thrombopoietin
Kimura, S. H., Roberts, A. W., Metcalf, D., & Alexander, W. S. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.1195 · Cited by 387 · see citing works
The relative spatial distributions of CFUs and CFUc in the normal mouse femur
Lord, B. I., Testa, N., & Hendry, J. (1975) · Blood · doi:10.1182/blood.v46.1.65.65 · Cited by 376 · see citing works
Haeckel, E. (1866) · Georg Reimer eBooks · doi:10.5962/bhl.title.101747 · Cited by 369 · see citing works
Ara, T., Tokoyoda, K., Sugiyama, T., Egawa, T., Kawabata, K., & Nagasawa, T. (2003) · Immunity · doi:10.1016/s1074-7613(03)00201-2 · Cited by 369 · see citing works
Dar, A., Goichberg, P., Shinder, V., Kalinkovich, A., Kollet, Ó., Netzer, N., Margalit, R., Zsak, M., Nagler, A., Hardan, I., et al. (2005) · Nature Immunology · doi:10.1038/ni1251 · Cited by 364 · see citing works
Kiel, M. J., Radice, G. L., & Morrison, S. J. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.06.001 · Cited by 343 · see citing works
Self-citationMultiple functions of Osterix are required for bone growth and homeostasis in postnatal mice
Zhou, X., Zhang, Z., Feng, J. Q., Dusevich, V., Sinha, K. M., Zhang, H., Darnay, B. G., & Crombrugghe, B. D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912855107 · Cited by 318 · see citing works
Spangrude, G. J., Brooks, D., & Tumas, D. B. (1995) · Blood · doi:10.1182/blood.v85.4.1006.bloodjournal8541006 · Cited by 316 · see citing works
Diabetes Impairs Hematopoietic Stem Cell Mobilization by Altering Niche Function
Ferraro, F., Lymperi, S., Méndez‐Ferrer, S., Sáez, B., Spencer, J. A., Yeap, B. Y., Masselli, E., Graiani, G., Prezioso, L., Rizzini, E. L., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002191 · Cited by 296 · see citing works
Self-citationNoncanonical Wnt Signaling Maintains Hematopoietic Stem Cells in the Niche
Sugimura, R., He, X., Venkatraman, A., Arai, F., Box, A., Semerad, C. L., Haug, J. S., Peng, L., Zhong, X.-B., Suda, T., et al. (2012) · Cell · doi:10.1016/j.cell.2012.05.041 · Cited by 294 · see citing works
Sungaran, R., Markovic, B., & Chong, B. H. (1997) · Blood · doi:10.1182/blood.v89.1.101 · Cited by 291 · see citing works
Pleiotrophin regulates the expansion and regeneration of hematopoietic stem cells
Himburg, H. A., Muramoto, G. G., Daher, P., Meadows, S. K., Russell, J. L., Doan, P. L., Chi, J., Salter, A. B., Lento, W. E., Reya, T., et al. (2010) · Nature Medicine · doi:10.1038/nm.2119 · Cited by 286 · see citing works
Tzeng, Y.-S., Li, H., Kang, Y.-L., Chen, W., Cheng, W., & Lai, D. (2010) · Blood · doi:10.1182/blood-2010-01-266833 · Cited by 279 · see citing works
Siminovitch, L., Till, J. E., & McCulloch, E. A. (1964) · Journal of Cellular and Comparative Physiology · doi:10.1002/jcp.1030640104 · Cited by 277 · see citing works
Yilmaz, Ö. H., Kiel, M. J., & Morrison, S. J. (2005) · Blood · doi:10.1182/blood-2005-05-2140 · Cited by 266 · see citing works
Self-citationGene Expression Commons: An Open Platform for Absolute Gene Expression Profiling
Seita, J., Sahoo, D., Rossi, D. J., Bhattacharya, D., Serwold, T. F., Inlay, M. A., Ehrlich, L. I. R., Fathman, J. W., Dill, D. L., & Weissman, I. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040321 · Cited by 261 · see citing works
Osteoblastic regulation of B lymphopoiesis is mediated by G s α-dependent signaling pathways
Wu, J. Y., Purton, L. E., Rodda, S. J., Chen, M., Weinstein, L. S., McMahon, A. P., Scadden, D. T., & Kronenberg, H. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802898105 · Cited by 245 · see citing works
Self-citationOsteoclasts promote the formation of hematopoietic stem cell niches in the bone marrow
Mansour, A., Abou‐Ezzi, G., Sitnicka, E., Jacobsen, S. E. W., Wakkach, A., & Blin‐Wakkach, C. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20110994 · Cited by 216 · see citing works
Hematopoietic Stem Cells Do Not Depend on N-Cadherin to Regulate Their Maintenance
Kiel, M. J., Acar, M., Radice, G. L., & Morrison, S. J. (2009) · Cell stem cell · doi:10.1016/j.stem.2008.10.005 · Cited by 198 · see citing works
Self-citationCharacterization of mouse lymphohematopoietic stem cells lacking spleen colony-forming activity
Jones, R., Collector, M. I., Barber, J. P., Vala, M., Fackler, M., May, W. S., Griffin, C. A., Hawkins, A., Zehnbauer, B., Hilton, A., et al. (1996) · Blood · doi:10.1182/blood.v88.2.487.bloodjournal882487 · Cited by 185 · see citing works
Matrix-Embedded Osteocytes Regulate Mobilization of Hematopoietic Stem/Progenitor Cells
Asada, N., Katayama, Y., Sato, M. M., Minagawa, K., Wakahashi, K., Kawano, H., Kawano, Y., Sada, A., Ikeda, K., Matsui, T., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.05.001 · Cited by 166 · see citing works
The relationship between bone, hemopoietic stem cells, and vasculature
Ellis, S. L., Grassinger, J., Jones, A. S., Borg, J., Camenisch, T. D., Haylock, D. N., Bertoncello, I., & Nilsson, S. K. (2011) · Blood · doi:10.1182/blood-2010-08-303800 · Cited by 159 · see citing works
Li, W., Johnson, S. A., Shelley, W. C., & Yöder, M. C. (2004) · Experimental Hematology · doi:10.1016/j.exphem.2004.09.001 · Cited by 151 · see citing works
Himburg, H. A., Harris, J. R., Ito, T., Daher, P., Russell, J. L., Quarmyne, M., Doan, P. L., Helms, K. L., Nakamura, M., Fixsen, E., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.002 · Cited by 147 · see citing works
Nakamura‐Ishizu, A., Okuno, Y., Omatsu, Y., Okabe, K., Morimoto, J. O., Uede, T., Nagasawa, T., Suda, T., & Kubota, Y. (2012) · Blood · doi:10.1182/blood-2011-11-393645 · Cited by 142 · see citing works
Strontium can increase some osteoblasts without increasing hematopoietic stem cells
Lymperi, S., Horwood, N. J., Marley, S. B., Gordon, M. Y., Cope, A. P., & Dazzi, F. (2007) · Blood · doi:10.1182/blood-2007-03-082800 · Cited by 137 · see citing works
Robo4 Cooperates with Cxcr4 to Specify Hematopoietic Stem Cell Localization to Bone Marrow Niches
Smith‐Berdan, S., Nguyen, A., Hassanein, D., Zimmer, M., Ugarte, F., Ciriza, J., Li, D., García‐Ojeda, M. E., Hinck, L., & Forsberg, E. C. (2011) · Cell stem cell · doi:10.1016/j.stem.2010.11.030 · Cited by 133 · see citing works
Knockdown of N-cadherin suppresses the long-term engraftment of hematopoietic stem cells
Hosokawa, K., Arai, F., Yoshihara, H., Iwasaki, H., Nakamura, Y., Gomei, Y., & Suda, T. (2010) · Blood · doi:10.1182/blood-2009-05-224857 · Cited by 130 · see citing works
Regional Localization within the Bone Marrow Influences the Functional Capacity of Human HSCs
Guezguez, B., Campbell, C. J. V., Boyd, A. L., Karanu, F., Casado, F. L., Cresce, C. D., Collins, T. J., Shapovalova, Z., Xenocostas, A., & Bhatia, M. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.06.015 · Cited by 125 · see citing works
Conditional Ablation of the Osteoblast Lineage in Col2.3Δtk Transgenic Mice
Višnjić, D., Kalajzić, I., Gronowicz, G., Aguila, H. L., Clark, S. H., Lichtler, A., & Rowe, D. W. (2001) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.2001.16.12.2222 · Cited by 110 · see citing works
Bone marrow dysfunction in mice lacking the cytokine receptor gp130 in endothelial cells
Yao, L., Yokota, T., Xia, L., Kincade, P. W., & McEver, R. P. (2005) · Blood · doi:10.1182/blood-2005-02-0671 · Cited by 106 · see citing works
Bromberg, O., Frisch, B. J., Weber, J. M., Porter, R. L., Civitelli, R., & Calvi, L. M. (2012) · Blood · doi:10.1182/blood-2011-09-377853 · Cited by 97 · see citing works
Hosokawa, K., Arai, F., Yoshihara, H., Iwasaki, H., Hembree, M. J., Yin, T., Nakamura, Y., Gomei, Y., Takubo, K., Shiama, H., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2009.04.013 · Cited by 97 · see citing works
Dissecting the Hematopoietic Microenvironment
Wolf, N. S. (1978) · Cell Proliferation · doi:10.1111/j.1365-2184.1978.tb00806.x · Cited by 94 · see citing works
Thrombopoietin Is Synthesized by Bone Marrow Stromal Cells
Guerriero, A., Worford, L., Holland, H. K., Guo, G.-R., Sheehan, K., & Waller, E. K. (1997) · Blood · doi:10.1182/blood.v90.9.3444 · Cited by 94 · see citing works
N-cadherin in osteolineage cells is not required for maintenance of hematopoietic stem cells
Greenbaum, A. M., Revollo, L., Woloszynek, J. R., Civitelli, R., & Link, D. C. (2012) · Blood · doi:10.1182/blood-2011-09-377457 · Cited by 94 · see citing works
Sl/Sld hematopoietic progenitors are deficient in situ.
Barker, J. E. (1994) · PubMed · Cited by 93 · see citing works
Thrombopoietin and the Hematopoietic Stem Cell
Kaushansky, K. (1998) · Blood · doi:10.1182/blood.v92.1.1.413a37_1_3 · Cited by 88 · see citing works
Integrating Physiological Regulation with Stem Cell and Tissue Homeostasis
Nakada, D., Levi, B. P., & Morrison, S. J. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.011 · Cited by 70 · see citing works
Self-citationHaeckel, E. (1992) · North-Eastern Hill University Library (North Eastern Hill University) · Cited by 69 · see citing works
Thrombopoietin and the Hematopoietic Stem Cell
Kaushansky, K. (2005) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1349.018 · Cited by 64 · see citing works
Wnt-inhibitory factor 1 dysregulation of the bone marrow niche exhausts hematopoietic stem cells
Schaniel, C., Sirabella, D., Qiu, J., Niu, X., Lemischka, I. R., & Moore, K. A. (2011) · Blood · doi:10.1182/blood-2010-09-305664 · Cited by 63 · see citing works
Barker, J. E. (1997) · PubMed · Cited by 58 · see citing works
Ueber Entwickelung und Ausbildung der Erythroblasten
Pappenheim, A. (1896) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/bf01969901 · Cited by 53 · see citing works
Dai, J. C., He, P., Chen, X., & Greenfield, E. M. (2005) · Bone · doi:10.1016/j.bone.2005.10.007 · Cited by 51 · see citing works
This Niche Is a Maze; An Amazing Niche
Hanoun, M., & Frenette, P. S. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.03.012 · Cited by 49 · see citing works
Resolving the Controversy about N-Cadherin and Hematopoietic Stem Cells
Li, P., & Zon, L. I. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.02.007 · Cited by 47 · see citing works
Dynamic expression of the Robo ligand Slit2 in bone marrow cell populations
Smith‐Berdan, S., Schepers, K., Ly, A., Passegue, E. A., & Forsberg, E. C. (2012) · Cell Cycle · doi:10.4161/cc.11.4.19146 · Cited by 27 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Mesenchymal stem cells use extracellular vesicles to outsource mitophagy and shuttle microRNAs
Phinney, D. G., Di Giuseppe, M., Njah, J., Sala, E., Shiva, S., St Croix, C. M., Stolz, D. B., Watkins, S. C., Di, Y. P., Leikauf, G. D., et al. (2015) · Nature Communications · doi:10.1038/ncomms9472 · Cited by 1,007 · see citing works
Metastatic heterogeneity of breast cancer: Molecular mechanism and potential therapeutic targets
Liang, Y., Zhang, H., Song, X., & Yang, Q. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.08.012 · Cited by 997 · see citing works
Angiocrine functions of organ-specific endothelial cells
Rafii, S., Butler, J. M., & Ding, B. (2016) · Nature · doi:10.1038/nature17040 · Cited by 948 · see citing works
The bone marrow microenvironment at single-cell resolution
Tikhonova, A. N., Dolgalev, I., Hu, H., Sivaraj, K. K., Hoxha, E., Cuesta-Domínguez, Á., Pinho, S., Akhmetzyanova, I., Gao, J., Witkowski, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1104-8 · Cited by 936 · see citing works
Perivascular Gli1+ Progenitors Are Key Contributors to Injury-Induced Organ Fibrosis
Kramann, R., Schneider, R. K., DiRocco, D. P., Machado, F., Fleig, S., Bondzie, P. A., Henderson, J. M., Ebert, B. L., & Humphreys, B. D. (2015) · Cell Stem Cell · doi:10.1016/j.stem.2014.11.004 · Cited by 922 · see citing works
A Cellular Taxonomy of the Bone Marrow Stroma in Homeostasis and Leukemia
Baryawno, N., Przybylski, D., Kowalczyk, M. S., Kfoury, Y. S., Sévère, N., Gustafsson, K. U., Kokkaliaris, K. D., Mercier, F., Tabaka, M., Hofree, M., et al. (2019) · Cell · doi:10.1016/j.cell.2019.04.040 · Cited by 882 · see citing works
Self-citationBaccin, C., Al-Sabah, J., Velten, L., Helbling, P. M., Grünschläger, F., Hernández-Malmierca, P., Nombela‐Arrieta, C., Steinmetz, L. M., Trumpp, A., & Haas, S. F. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0439-6 · Cited by 858 · see citing works
Ambrosi, T. H., Scialdone, A., Graja, A., Gohlke, S., Jank, A.-M., Bocian, C., Woelk, L., Fan, H., Logan, D. W., Schürmann, A., et al. (2017) · Cell Stem Cell · doi:10.1016/j.stem.2017.02.009 · Cited by 856 · see citing works
Chronic variable stress activates hematopoietic stem cells
Heidt, T., Sager, H. B., Courties, G., Dutta, P., Iwamoto, Y., Zaltsman, A., von zur Muhlen, C., Bode, C., Fricchione, G. L., Denninger, J., et al. (2014) · Nature Medicine · doi:10.1038/nm.3589 · Cited by 803 · see citing works
Hematopoietic stem cell niche maintenance during homeostasis and regeneration
Mendelson, A., & Frenette, P. S. (2014) · Nature Medicine · doi:10.1038/nm.3647 · Cited by 783 · see citing works
The role of myeloid cells in cancer therapies
Engblom, C., Pfirschke, C., & Pittet, M. J. (2016) · Nature Reviews Cancer · doi:10.1038/nrc.2016.54 · Cited by 788 · see citing works
Osteoimmunology: evolving concepts in bone–immune interactions in health and disease
Tsukasaki, M., & Takayanagi, H. (2019) · Nature reviews. Immunology · doi:10.1038/s41577-019-0178-8 · Cited by 789 · see citing works
Single-cell Wnt signaling niches maintain stemness of alveolar type 2 cells
Nabhan, A. N., Brownfield, D., Harbury, P. B., Krasnow, M. A., & Desai, T. (2018) · Science · doi:10.1126/science.aam6603 · Cited by 731 · see citing works
Distinct bone marrow blood vessels differentially regulate haematopoiesis
Itkin, T., Gur‐Cohen, S., Spencer, J. A., Schajnovitz, A., Ramasamy, S. K., Kusumbe, A. P., Ledergor, G., Jung, Y., Milo, I., Poulos, M. G., et al. (2016) · Nature · doi:10.1038/nature17624 · Cited by 709 · see citing works
Self-citationAdult haematopoietic stem cell niches
Crane, G. M., Jeffery, E., & Morrison, S. J. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.53 · Cited by 712 · see citing works
Self-citationMicroRNAs as regulatory elements in immune system logic
Mehta, A., & Baltimore, D. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2016.40 · Cited by 704 · see citing works
Deep imaging of bone marrow shows non-dividing stem cells are mainly perisinusoidal
Acar, M., Kocherlakota, K. S., Murphy, M. M., Peyer, J. G., Oguro, H., Inra, C. N., Jaiyeola, C., Zhao, Z., Luby‐Phelps, K., & Morrison, S. J. (2015) · Nature · doi:10.1038/nature15250 · Cited by 702 · see citing works
Self-citationImpact of Obesity and Metabolic Syndrome on Immunity
Andersen, C. J., Murphy, K. E., & Fernandez, M. L. (2016) · Advances in Nutrition · doi:10.3945/an.115.010207 · Cited by 701 · see citing works
Biological functions of mesenchymal stem cells and clinical implications
Naji, A., Eitoku, M., Favier, B., Deschaseaux, F., Rouas‐Freiss, N., & Suganuma, N. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03125-1 · Cited by 628 · see citing works
Modulating the stem cell niche for tissue regeneration
Lane, S., Williams, D. A., & Watt, F. M. (2014) · Nature Biotechnology · doi:10.1038/nbt.2978 · Cited by 616 · see citing works
Herisson, F., Frodermann, V., Courties, G., Rohde, D., Sun, Y., Vandoorne, K., Wojtkiewicz, G. R., Masson, G. S., Vinegoni, C., Kim, J., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0213-2 · Cited by 610 · see citing works
The Wnt Signaling Pathway in Cancer
Duchartre, Y., Kim, Y.-M., & Kahn, M. (2015) · Critical reviews in oncology/hematology · doi:10.1016/j.critrevonc.2015.12.005 · Cited by 498 · see citing works
Mesenchymal Cell Contributions to the Stem Cell Niche
Kfoury, Y. S., & Scadden, D. T. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.02.019 · Cited by 548 · see citing works
Self-citationOsteoimmunology: The conceptual framework unifying the immune and skeletal systems
Okamoto, K., Nakashima, T., Shinohara, M., Negishi-Koga, T., Komatsu, N., Terashima, A., Sawa, S., Nitta, T., & Takayanagi, H. (2017) · Physiological Reviews · doi:10.1152/physrev.00036.2016 · Cited by 534 · see citing works
Anatomical, Physiological, and Functional Diversity of Adipose Tissue
Zwick, R. K., Guerrero‐Juarez, C. F., Horsley, V., & Plikus, M. V. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.12.002 · Cited by 526 · see citing works
It Takes Two to Tango: Coupling of Angiogenesis and Osteogenesis for Bone Regeneration
Grosso, A., Burger, M. G., Lunger, A., Schaefer, D. J., Banfi, A., & Maggio, N. D. (2017) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2017.00068 · Cited by 452 · see citing works
Kumar, B., García, M., Weng, L., Jung, X., Murakami, J. L., Hu, X., McDonald, T., Lin, A., Kumar, A. R., DiGiusto, D. L., et al. (2017) · Leukemia · doi:10.1038/leu.2017.259 · Cited by 445 · see citing works
Long-term ex vivo haematopoietic-stem-cell expansion allows nonconditioned transplantation
Wilkinson, A. C., Ishida, R., Kikuchi, M., Sudo, K., Morita, M., Crisostomo, R. V., Yamamoto, R., Loh, K. M., Nakamura, Y., Watanabe, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1244-x · Cited by 411 · see citing works
Blood flow controls bone vascular function and osteogenesis
Ramasamy, S. K., Kusumbe, A. P., Schiller, M., Zeuschner, D., Bixel, M. G., Milia, C., Gamrekelashvili, J., Limbourg, A., Medvinsky, A., Santoro, M. M., et al. (2016) · Nature Communications · doi:10.1038/ncomms13601 · Cited by 433 · see citing works
Mesenchymal stem cells in fibrotic disease
El Agha, E., Kramann, R., Schneider, R. K., Li, X., Seeger, W., Humphreys, B. D., & Bellusci, S. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.07.011 · Cited by 430 · see citing works
Normal and Leukemic Stem Cell Niches: Insights and Therapeutic Opportunities
Schepers, K., Campbell, T., & Passegué, E. (2015) · Cell Stem Cell · doi:10.1016/j.stem.2015.02.014 · Cited by 416 · see citing works
Bone physiology as inspiration for tissue regenerative therapies
Lopes, D., Martins‐Cruz, C., Oliveira, M. B., & Mano, J. F. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.09.028 · Cited by 437 · see citing works
Proliferation and recruitment contribute to myocardial macrophage expansion in chronic heart failure
Sager, H., Hulsmans, M., Lavine, K. J., Moreira, M. B., Heidt, T., Courties, G., Sun, Y., Iwamoto, Y., Tricot, B., Khan, O. F., et al. (2016) · Circulation Research · doi:10.1161/circresaha.116.309001 · Cited by 377 · see citing works
Transforming growth factor‐β in stem cells and tissue homeostasis
Xu, X., Zheng, L., Yuan, Q., Zhen, G., Crane, J. L., Zhou, X., & Cao, X. (2018) · Bone Research · doi:10.1038/s41413-017-0005-4 · Cited by 414 · see citing works
Cai, Y., Song, W., Li, J., Jing, Y., Liang, C., Zhang, L., Zhang, X., Zhang, W., Liu, B., An, Y., et al. (2022) · Science China Life Sciences · doi:10.1007/s11427-022-2161-3 · Cited by 436 · see citing works
Biodegradable materials for bone defect repair
Wei, S., Ma, J., Xu, L., Gu, X., & Ma, X. (2020) · Military Medical Research · doi:10.1186/s40779-020-00280-6 · Cited by 412 · see citing works
Bianco, P. (2014) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100913-013132 · Cited by 400 · see citing works
Tissue clearing of both hard and soft tissue organs with the PEGASOS method
Jing, D., Zhang, S., Luo, W., Gao, X., Men, Y., Ma, C., Liu, X., Yi, Y., Bugde, A., Zhou, B. O., et al. (2018) · Cell Research · doi:10.1038/s41422-018-0049-z · Cited by 401 · see citing works
Design, Materials, and Mechanobiology of Biodegradable Scaffolds for Bone Tissue Engineering
Peña, M. A. V., Narváez-Tovar, C. A., & Garzón–Alvarado, D. A. (2015) · BioMed Research International · doi:10.1155/2015/729076 · Cited by 397 · see citing works
Osteoclasts: more than ‘bone eaters’
Charles, J. F., & Aliprantis, A. O. (2014) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2014.06.001 · Cited by 391 · see citing works
Osteoblasts remotely supply lung tumors with cancer-promoting SiglecF high neutrophils
Engblom, C., Pfirschke, C., Žilionis, R., Martins, J. D. S., Bos, S. A., Courties, G., Rickelt, S., Sévère, N., Baryawno, N., Faget, J., et al. (2017) · Science · doi:10.1126/science.aal5081 · Cited by 388 · see citing works
Self-citationInflamm-aging of hematopoiesis, hematopoietic stem cells, and the bone marrow microenvironment
Kovtonyuk, L. V., Fritsch, K., Feng, X., Manz, M. G., & Takizawa, H. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00502 · Cited by 371 · see citing works
Mesenchymal Stromal/Stem Cells in Regenerative Medicine and Tissue Engineering
Fitzsimmons, R., Mazurek, M. S., Soos, A., & Simmons, C. A. (2018) · Stem Cells International · doi:10.1155/2018/8031718 · Cited by 358 · see citing works
Hoxb5 marks long-term haematopoietic stem cells and reveals a homogenous perivascular niche
Chen, J. Y., Miyanishi, M., Wang, S. K., Yamazaki, S., Sinha, R., Kao, K. S., Seita, J., Sahoo, D., Nakauchi, H., & Weissman, I. L. (2016) · Nature · doi:10.1038/nature16943 · Cited by 345 · see citing works
Causes and Consequences of Hematopoietic Stem Cell Heterogeneity
Haas, S. F., Trumpp, A., & Milsom, M. D. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.04.003 · Cited by 330 · see citing works
Hematopoietic Stem Cell Arrival Triggers Dynamic Remodeling of the Perivascular Niche
Tamplin, O. J., Durand, E. M., Carr, L. A., Childs, S. J., Hagedorn, E. J., Li, P., Yzaguirre, A. D., Speck, N. A., & Zon, L. I. (2015) · Cell · doi:10.1016/j.cell.2014.12.032 · Cited by 342 · see citing works
Enhancing Hematopoietic Stem Cell Transplantation Efficacy by Mitigating Oxygen Shock
Mantel, C., O’Leary, H. A., Chitteti, B. R., Huang, X., Cooper, S. H., Hangoc, G., Brustovetsky, N., Srour, E. F., Lee, M. R., Messina‐Graham, S., et al. (2015) · Cell · doi:10.1016/j.cell.2015.04.054 · Cited by 335 · see citing works
Inhibition of Endosteal Vascular Niche Remodeling Rescues Hematopoietic Stem Cell Loss in AML
Duarte, D., Hawkins, E., Akinduro, O., Ang, H., Filippo, K. D., Kong, I. Y., Haltalli, M., Ruivo, N., Straszkowski, L., Vervoort, S., et al. (2018) · Cell Stem Cell · doi:10.1016/j.stem.2017.11.006 · Cited by 292 · see citing works
Bioinspired surface modification of orthopedic implants for bone tissue engineering
Hu, C. Q., Ashok, D., Nisbet, D. R., & Gautam, V. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119366 · Cited by 324 · see citing works
The Dynamics of Apoptotic Cell Clearance
Elliott, M. R., & Ravichandran, K. S. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.06.029 · Cited by 314 · see citing works
Metastasis prevention by targeting the dormant niche
Ghajar, C. M. (2015) · Nature reviews. Cancer · doi:10.1038/nrc3910 · Cited by 317 · see citing works
Ho, Y.-H., del Toro, R., Rivera-Torres, J., Rak, J., Korn, C., García-García, A., Macías, D., González-Gómez, C., del Monte, A., Wittner, M., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.06.007 · Cited by 315 · see citing works
Hematopoietic progenitor cells as integrative hubs for adaptation to and fine-tuning of inflammation
Chavakis, T., Mitroulis, I., & Hajishengallis, G. (2019) · Nature Immunology · doi:10.1038/s41590-019-0402-5 · Cited by 318 · see citing works
Sasaki, N., Sachs, N., Wiebrands, K., Ellenbroek, S. I. J., Fumagalli, A., Lyubimova, A., Begthel, H., van den Born, M., van Es, J. H., Karthaus, W. R., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1607327113 · Cited by 314 · see citing works
A network of trans-cortical capillaries as mainstay for blood circulation in long bones
Grüneboom, A., Hawwari, I., Weidner, D., Culemann, S., Müller, S., Henneberg, S., Brenzel, A., Merz, S. F., Bornemann, L., Zec, K., et al. (2018) · Nature Metabolism · doi:10.1038/s42255-018-0016-5 · Cited by 308 · see citing works
Molecular biomarkers in acute myeloid leukemia
Prada‐Arismendy, J., Arroyave-Ospina, J. C., & Röthlisberger, S. (2016) · Blood Reviews · doi:10.1016/j.blre.2016.08.005 · Cited by 303 · see citing works
On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology
Chou, D. B., Frismantas, V., Milton, Y., David, R. M., Pop-Damkov, P., Ferguson, D., MacDonald, A., Bölükbaşı, Ö. V., Joyce, C. E., Teixeira, L. M., et al. (2020) · Nature Biomedical Engineering · doi:10.1038/s41551-019-0495-z · Cited by 301 · see citing works
Bandyopadhyay, S., Duffy, M. P., Ahn, K. J., Sussman, J. H., Pang, M., Smith, D., Duncan, G., Zhang, I., Huang, J., Lin, Y., et al. (2024) · Cell · doi:10.1016/j.cell.2024.04.013 · Cited by 300 · see citing works
Inhibition of the prostaglandin-degrading enzyme 15-PGDH potentiates tissue regeneration
Zhang, Y., Desai, A. B., Yang, S. Y., Bae, K. B., Antczak, M. I., Fink, S. P., Tiwari, S. R., Willis, J. E., Williams, N. S., Dawson, D. M., et al. (2015) · Science · doi:10.1126/science.aaa2340 · Cited by 297 · see citing works
Niches that regulate stem cells and hematopoiesis in adult bone marrow
Comazzetto, S., Shen, B., & Morrison, S. J. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.05.018 · Cited by 289 · see citing works
Self-citationFrodermann, V., Rohde, D., Courties, G., Severe, N., Schloss, M. J., Amatullah, H., McAlpine, C. S., Cremer, S., Hoyer, F. F., Ji, F., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0633-x · Cited by 292 · see citing works
Self-citationEr, E. E., Valiente, M., Ganesh, K., Zou, Y., Agrawal, S., Hu, J. Y., Griscom, B., Rosenblum, M. K., Boire, A. A., Brogi, E., et al. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0138-8 · Cited by 282 · see citing works
Gomes, A. C., Hara, T., Lim, V., Herndler‐Brandstetter, D., Nevius, E., Sugiyama, T., Tani‐ichi, S., Schlenner, S., Richie, E. R., Rodewald, H.-R., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.11.004 · Cited by 288 · see citing works
Niche heterogeneity in the bone marrow
Birbrair, A., & Frenette, P. S. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13016 · Cited by 283 · see citing works
Saito, Y., Chapple, R., Lin, A., Kitano, A., & Nakada, D. (2015) · Cell Stem Cell · doi:10.1016/j.stem.2015.08.019 · Cited by 245 · see citing works
Takizawa, H., Fritsch, K., Kovtonyuk, L. V., Saito, Y., Yakkala, C., Jacobs, K., Ahuja, A. K., Lopes, M., Hausmann, A., Hardt, W., et al. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.06.013 · Cited by 272 · see citing works
Cellular and epigenetic drivers of stem cell ageing
Ermolaeva, M., Neri, F., Ori, A., & Rudolph, K. L. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0020-3 · Cited by 272 · see citing works
New paradigms on hematopoietic stem cell differentiation
Cheng, H., Zheng, Z., & Cheng, T. (2019) · Protein & Cell · doi:10.1007/s13238-019-0633-0 · Cited by 275 · see citing works
Neural Regulation of Hematopoiesis, Inflammation, and Cancer
Hanoun, M., Maryanovich, M., Arnal-Estapé, A., & Frenette, P. S. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.026 · Cited by 265 · see citing works
Mesenchymal stromal cells: Putative microenvironmental modulators become cell therapy
Krampera, M., & Blanc, K. L. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.09.006 · Cited by 265 · see citing works
Leukaemogenic effects of Ptpn11 activating mutations in the stem cell microenvironment
Dong, L., Yu, W., Zheng, H., Loh, M. L., Bunting, S. T., Pauly, M. G., Huang, G., Zhou, M., Broxmeyer, H. E., Scadden, D. T., et al. (2016) · Nature · doi:10.1038/nature20131 · Cited by 260 · see citing works
Self-citationEndothelial cells translate pathogen signals into G-CSF–driven emergency granulopoiesis
Boettcher, S., Gerosa, R. C., Radpour, R., Bauer, J., Ampenberger, F., Heikenwälder, M. F., Köpf, M., & Manz, M. G. (2014) · Blood · doi:10.1182/blood-2014-04-570762 · Cited by 260 · see citing works
Myeloid cell contributions to cardiovascular health and disease
Nahrendorf, M. (2018) · Nature Medicine · doi:10.1038/s41591-018-0064-0 · Cited by 257 · see citing works
Treweek, J. B., Chan, K. Y., Flytzanis, N. C., Yang, B., Deverman, B. E., Greenbaum, A., Lignell, A., Xiao, C., Cai, L., Ladinsky, M. S., et al. (2015) · Nature Protocols · doi:10.1038/nprot.2015.122 · Cited by 255 · see citing works
The endothelium–bone axis in development, homeostasis and bone and joint disease
Tuckermann, J., & Adams, R. H. (2021) · Nature Reviews Rheumatology · doi:10.1038/s41584-021-00682-3 · Cited by 258 · see citing works
Targeting Interleukin-1β Reduces Leukocyte Production After Acute Myocardial Infarction
Sager, H. B., Heidt, T., Hulsmans, M., Dutta, P., Courties, G., Sebas, M., Wojtkiewicz, G. R., Tricot, B., Iwamoto, Y., Sun, Y., et al. (2015) · Circulation · doi:10.1161/circulationaha.115.016160 · Cited by 250 · see citing works
CXCL12-Producing Vascular Endothelial Niches Control Acute T Cell Leukemia Maintenance
Pitt, L. A., Tikhonova, A. N., Hu, H., Trimarchi, T., King, B., Gong, Y., Sánchez-Martín, M., Tsirigos, A., Littman, D. R., Ferrando, A. A., et al. (2015) · Cancer Cell · doi:10.1016/j.ccell.2015.05.002 · Cited by 252 · see citing works
Self-citationStem cell dynamics in homeostasis and cancer of the intestine
Vermeulen, L., & Snippert, H. J. G. (2014) · Nature reviews. Cancer · doi:10.1038/nrc3744 · Cited by 250 · see citing works
Regulation of hematopoietic and leukemic stem cells by the immune system
Riether, C., Schürch, C. M., & Ochsenbein, A. F. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.89 · Cited by 246 · see citing works
CD44: More than a mere stem cell marker
Morath, I., Hartmann, T. N., & Orian‐Rousseau, V. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.09.009 · Cited by 250 · see citing works
Hirata, Y., Furuhashi, K., Ishii, H., Li, H. W., Pinho, S., Ding, L., Robson, S. C., Frenette, P. S., & Fujisaki, J. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.01.017 · Cited by 249 · see citing works
Biasco, L., Pellin, D., Scala, S., Dionisio, F., Basso-Ricci, L., Leonardelli, L., Scaramuzza, S., Baricordi, C., Ferrua, F., Cicalese, M. P., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.04.016 · Cited by 243 · see citing works
Identity Noise and Adipogenic Traits Characterize Dermal Fibroblast Aging
Salzer, M. C., Lafzi, A., Berenguer, A., Youssif, C., Castellanos‐Martín, A., Solanas, G., Peixoto, F. O., Attolini, C. S., Prats, N., Aguilera, M., et al. (2018) · Cell · doi:10.1016/j.cell.2018.10.012 · Cited by 243 · see citing works
Microglial Dynamics During Human Brain Development
Menassa, D. A., & Gómez‐Nicola, D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01014 · Cited by 238 · see citing works
Ischemic Stroke Activates Hematopoietic Bone Marrow Stem Cells
Courties, G., Hérisson, F., Sager, H. B., Heidt, T., Ye, Y., Wei, Y., Sun, Y., Sévère, N., Dutta, P., Scharff, J., et al. (2014) · Circulation Research · doi:10.1161/circresaha.116.305207 · Cited by 240 · see citing works
Self-citationThe kindlin family: functions, signaling properties and implications for human disease
Rognoni, E., Ruppert, R., & Fässler, R. (2016) · Journal of Cell Science · doi:10.1242/jcs.161190 · Cited by 241 · see citing works
Lee, H. J., Bao, S., Qian, Y., Geula, S., Leslie, J. S., Zhang, C., Hanna, J. H., & Ding, L. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0318-1 · Cited by 237 · see citing works
The analysis, roles and regulation of quiescence in hematopoietic stem cells
Nakamura‐Ishizu, A., Takizawa, H., & Suda, T. (2014) · Development · doi:10.1242/dev.106575 · Cited by 229 · see citing works
Mapping Distinct Bone Marrow Niche Populations and Their Differentiation Paths
Wolock, S. L., Krishnan, I., Tenen, D. E., Matkins, V. R., Camacho, V., Patel, S. B., Agarwal, P., Bhatia, R., Tenen, D. G., Klein, A. M., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.031 · Cited by 229 · see citing works
Haematopoietic stem cell self-renewal in vivo and ex vivo
Wilkinson, A. C., Igarashi, K. J., & Nakauchi, H. (2020) · Nature Reviews Genetics · doi:10.1038/s41576-020-0241-0 · Cited by 226 · see citing works
Stem cell homing: From physiology to therapeutics
Liesveld, J. L., Sharma, N., & Aljitawi, O. S. (2020) · Stem Cells · doi:10.1002/stem.3242 · Cited by 222 · see citing works
Aging: A Temporal Dimension for Neutrophils
Adrover, J. M., Nicolás-Ávila, J. Á., & Hidalgo, A. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.03.005 · Cited by 223 · see citing works
Conversion of adult endothelium to immunocompetent haematopoietic stem cells
Lis, R., Karrasch, C. C., Poulos, M. G., Kunar, B., Redmond, D., Durán, J. G. B., Badwe, C. R., Schachterle, W., Ginsberg, M. D., Xiang, J., et al. (2017) · Nature · doi:10.1038/nature22326 · Cited by 222 · see citing works
Myocardial Infarction Activates CCR2+ Hematopoietic Stem and Progenitor Cells
Dutta, P., Sager, H. B., Stengel, K. R., Naxerova, K., Courties, G., Sáez, B., Silberstein, L., Heidt, T., Sebas, M., Sun, Y., et al. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.04.008 · Cited by 219 · see citing works
Self-citationMitchell, C. A., Verovskaya, E. V., Calero‐Nieto, F. J., Olson, O. C., Swann, J. W., Wang, X., Hérault, A., Dellorusso, P. V., Zhang, S. Y., Svendsen, A. F., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-022-01053-0 · Cited by 219 · see citing works
Matrix metalloproteinases in stem cell regulation and cancer
Kessenbrock, K., Wang, C., & Werb, Z. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.01.022 · Cited by 215 · see citing works
Mirantes, C., Passegué, E., & Pietras, E. M. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.08.017 · Cited by 211 · see citing works
Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss
Hu, Y., Li, X., Zhang, Q., Gu, Z., Luo, Y., Guo, J., Wang, X., Jing, Y., Chen, X., & Su, J. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.02.014 · Cited by 210 · see citing works
Bioceramics to regulate stem cells and their microenvironment for tissue regeneration
Zhou, Y., Wu, C., & Chang, J. (2018) · Materials Today · doi:10.1016/j.mattod.2018.07.016 · Cited by 209 · see citing works
Nrf2: Redox and Metabolic Regulator of Stem Cell State and Function
Dai, X., Yan, X., Wintergerst, K. A., Cai, L., Keller, B. B., & Tan, Y. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.09.007 · Cited by 205 · see citing works
- Authors
- Morrison, S. J., & Scadden, D. T.
- Affiliations
- Howard Hughes Medical Institute (US)
- Harvard University (US)
- Corresponding author
- Morrison, Sean J.
- Scadden, David T.
- Venue
- Nature
- Published
- 2014-01
- Volume
- 505
- Issue
- 7483
- Pages
- 327-334
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4514480
- OpenAlex
- W2149053153
- Semantic Scholar
- 63cdd906a38c49f8d452a64cb77d5a597cfbfb38
- Cited by
- 2,451
- References
- 130
- Citations by year
- 2026: 139 · 2025: 176 · 2024: 141 · 2023: 177 · 2022: 194 · 2021: 210 · 2020: 226 · 2019: 225 · 2018: 240 · 2017: 223 · 2016: 225 · 2015: 184 · 2014: 89
- FWCI
- 36.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Heart, Lung, and Blood Institute (HL096372, R01HL044851, R03HL096372, HL044851, HL097760, R01HL097760)
- National Institute of Biomedical Imaging and Bioengineering (R01EB014703, EB014703)
- Topics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Health Sciences › Medicine › Hematology › Multiple Myeloma Research and Treatments
- Keywords
- hematopoietic stem cells, bone marrow microenvironment, hematopoiesis, perivascular niche, mesenchymal stem cells, endothelial cells, trabecular bone, endosteum, stem cell niche
- MeSH terms
- Animals, Bone and Bones, Bone Marrow, Hematopoietic Stem Cells, Humans, Osteoblasts, Endothelial Cells, Stem Cell Niche, Mesenchymal Stem Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review