The DOI matches its Crossref record; 186 of the 186 references it cites were found in a registry or an index.
Adult haematopoietic stem cell niches
Abstract
Stem cell niches are specialized microenvironments that promote the maintenance of stem cells and regulate their function. Recent advances have improved our understanding of the niches that maintain adult haematopoietic stem cells (HSCs). These advances include new markers for HSCs and niche cells, systematic analyses of the expression patterns of niche factors, genetic tools for functionally identifying niche cells in vivo, and improved imaging techniques. Together, they have shown that HSC niches are perivascular in the bone marrow and spleen. Endothelial cells and mesenchymal stromal cells secrete factors that promote HSC maintenance in these niches, but other cell types also directly or indirectly regulate HSC niches.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Surface tethering can also be achieved with nanotechnologies, such as nano-imprint lithography, electron-beam, and electrospinning, can fabricate substrates with nanopillars, nanopits, or nanochannels, mimicking the basement membrane for 3D organoid culture90.”
From Organoids (2022) · cites this paper as [90]
Citations
Cites
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
Mesenchymal 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
Kiel, 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
Self-citationProgenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1
Ceradini, D. J., Kulkarni, A. R., Callaghan, M. J., Tepper, O. M., Bastidas, N., Kleinman, M. E., Capla, J. M., Galiano, R. D., Levine, J. P., & Gurtner, G. C. (2004) · Nature Medicine · doi:10.1038/nm1075 · Cited by 2,600
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 2,531
The bone marrow niche for haematopoietic stem cells
Morrison, S. J., & Scadden, D. T. (2014) · Nature · doi:10.1038/nature12984 · Cited by 2,451
Self-citationSugiyama, T., Kohara, H., Noda, M., & Nagasawa, T. (2006) · Immunity · doi:10.1016/j.immuni.2006.10.016 · Cited by 2,419
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
The relationship between the spleen colony-forming cell and the haemopoietic stem cell.
Schofield, R. (1978) · PubMed · Cited by 2,304
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
Coupling of angiogenesis and osteogenesis by a specific vessel subtype in bone
Kusumbe, A. P., Ramasamy, S. K., & Adams, R. H. (2014) · Nature · doi:10.1038/nature13145 · Cited by 2,155
Endothelial 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 2,031
Self-citationStem 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 2,026
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
Definitive Hematopoiesis Is Autonomously Initiated by the AGM Region
Medvinsky, A., & Dzierzak, E. A. (1996) · Cell · doi:10.1016/s0092-8674(00)80165-8 · Cited by 1,548
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
Zsebo, K. M., Williams, D. A., Geissler, E. N., Broudy, V. C., Martin, F. H., Atkins, H. L., Hsu, R.-Y., Birkett, N. C., Okino, K. H., Murdock, D. C., et al. (1990) · Cell · doi:10.1016/0092-8674(90)90302-u · Cited by 1,394
Zhou, B. O., Yue, R., Murphy, M. M., Peyer, J. G., & Morrison, S. J. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.06.008 · Cited by 1,381
Self-citationCXCL12 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
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 1,349
Self-citationG-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
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
Arteriolar 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 1,290
Stimulation of megakaryocytopoiesis and thrombopoiesis by the c-Mpl ligand
de Sauvage, F. J., Hass, P. E., Spencer, S. D., Malloy, B., Gurney, A. L., Spencer, S. A., Darbonne, W. C., Henzel, W. J., Wong, S. C., Kuang, W.-J., et al. (1994) · Nature · doi:10.1038/369533a0 · Cited by 1,270
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
Huang, E. J., Nocka, K. H., Beier, D. R., Chu, T.-Y., Buck, J., Lahm, H., Wellner, D., Leder, P., & Besmer, P. (1990) · Cell · doi:10.1016/0092-8674(90)90303-v · Cited by 1,149
Bone-marrow adipocytes as negative regulators of the haematopoietic microenvironment
Naveiras, O., Nardi, V., Wenzel, P. L., Hauschka, P. V., Fahey, F., & Daley, G. Q. (2009) · Nature · doi:10.1038/nature08099 · Cited by 1,129
Bone 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
Granulocyte colony-stimulating factor and its receptor
Demetri, G. D., & Griffin, J. D. (1991) · Blood · doi:10.1182/blood.v78.11.2791.2791 · Cited by 1,066
Haematopoietic stem cells derive directly from aortic endothelium during development
Bertrand, J. Y., Chi, N. C., Santoso, B., Teng, S., Stainier, D. Y. R., & Traver, D. (2010) · Nature · doi:10.1038/nature08738 · Cited by 1,025
Kaushansky, K., Lok, S., Holly, R. D., Broudy, V. C., Lin, N. L., Bailey, M. C., Forstrom, J. W., Buddle, M. M., Oort, P. J., Hagen, F. S., et al. (1994) · Nature · doi:10.1038/369568a0 · Cited by 1,024
Expression of Cre recombinase in the developing mouse limb bud driven by a Prxl enhancer
Logan, M., Martin, J. F., Nagy, A., Lobe, C., Olson, E., & Tabin, C. (2002) · Genesis · doi:10.1002/gene.10092 · Cited by 1,022
Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter
Chen, M. J., Yokomizo, T., Zeigler, B. M., Dzierzak, E. A., & Speck, N. A. (2009) · Nature · doi:10.1038/nature07619 · Cited by 1,016
Blood stem cells emerge from aortic endothelium by a novel type of cell transition
Kissa, K., & Herbomel, P. (2010) · Nature · doi:10.1038/nature08761 · Cited by 961
Maes, C., Kobayashi, T., Selig, M. K., Torrekens, S., Roth, S. I., Mackem, S., Carmeliet, G., & Kronenberg, H. M. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.07.010 · Cited by 940
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
Identification of a ligand for the c-kit proto-oncogene
Williams, D. E., Eisenman, J., Baird, A. M., Rauch, C. T., Ness, K. V., March, C. J., Park, L. S., Martin, U., Mochizukl, D. Y., Boswell, H. S., et al. (1990) · Cell · doi:10.1016/0092-8674(90)90297-r · Cited by 920
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 914
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 912
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
Quiescent haematopoietic stem cells are activated by IFN-γ in response to chronic infection
Baldridge, M. T., King, K. Y., Boles, N. C., Weksberg, D. C., & Goodell, M. A. (2010) · Nature · doi:10.1038/nature09135 · Cited by 877
Distribution 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
Anderson, D. M., Lyman, S. D., Baird, A. M., Wignall, J. M., Eisenman, J. R., Rauch, C. T., March, C. J., Boswell, H. S., Gimpel, S. D., Cosman, D. J., et al. (1990) · Cell · doi:10.1016/0092-8674(90)90304-w · Cited by 827
Granulocyte colony-stimulating factor and its receptor
Demetri, G. D., & Griffin, J. (1991) · Blood · doi:10.1182/blood.v78.11.2791.bloodjournal78112791 · Cited by 825
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
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
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
Clonal dynamics of native haematopoiesis
Sun, J., Ramos, A., Chapman, B., Johnnidis, J. B., Le, L., Ho, Y.-J., Klein, A. M., Hofmann, O., & Camargo, F. D. (2014) · Nature · doi:10.1038/nature13824 · Cited by 803
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
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
Cellular Niches Controlling B Lymphocyte Behavior within Bone Marrow during Development
Tokoyoda, K., Egawa, T., Sugiyama, T., Choi, B.-I., & Nagasawa, T. (2004) · Immunity · doi:10.1016/j.immuni.2004.05.001 · Cited by 796
Zsebo, K. M., Wypych, J., McNiece, I., Lu, H. S., Smith, K. A., Karkare, S. B., Sachdev, R. K., Yuschenkoff, V. N., Birkett, N. C., Williams, L. R., et al. (1990) · Cell · doi:10.1016/0092-8674(90)90300-4 · Cited by 786
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 785
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
Osteoclasts 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
Fundamental properties of unperturbed haematopoiesis from stem cells in vivo
Busch, K., Klapproth, K., Barile, M., Flossdorf, M., Holland-Letz, T., Schlenner, S. M., Reth, M., Höfer, T., & Rodewald, H.-R. (2015) · Nature · doi:10.1038/nature14242 · Cited by 769
Identification and Specification of the Mouse Skeletal Stem Cell
Chan, C. K. F., Seo, E. Y., Chen, J. Y., Lo, D. D., McArdle, A., Sinha, R., Tevlin, R., Seita, J., Vincent-Tompkins, J., Wearda, T. L., et al. (2015) · Cell · doi:10.1016/j.cell.2014.12.002 · Cited by 763
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 757
The kit ligand: A cell surface molecule altered in steel mutant fibroblasts
Flanagan, J. G., & Leder, P. (1990) · Cell · doi:10.1016/0092-8674(90)90299-t · Cited by 747
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
Stier, S., Ko, Y. D., Forkert, R., Lutz, C., Neuhaus, T., Grünewald, E., Cheng, T., Dombkowski, D., Calvi, L. M., Rittling, S. R., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041992 · Cited by 733
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 729
Self-citationPrimary structure and functional expression of rat and human stem cell factor DNAs
Martin, F. H., Suggs, S. V., Langley, K. E., Lu, H. S., Ting, J., Okino, K. H., Morris, C. F., McNiece, I., Jacobsen, F. W., Mendlaz, E. A., et al. (1990) · Cell · doi:10.1016/0092-8674(90)90301-t · Cited by 719
Origin of monocytes and macrophages in a committed progenitor
Hettinger, J., Richards, D. M., Hansson, J., Barra, M. M., Joschko, A.-C., Krijgsveld, J., & Feuerer, M. (2013) · Nature Immunology · doi:10.1038/ni.2638 · Cited by 706
Oguro, H., Ding, L., & Morrison, S. J. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.05.014 · Cited by 692
Self-citationFate tracing reveals the endothelial origin of hematopoietic stem cells
Zovein, A. C., Hofmann, J. J., Lynch, M., French, W. J., Turlo, K. A., Yang, Y., Becker, M. S., Zanetta, L., Dejana, E., Gasson, J. C., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.09.018 · Cited by 691
Megakaryocytes regulate hematopoietic stem cell quiescence through CXCL4 secretion
Bruns, I., Lucas, D., Pinho, S., Ahmed, J. U., Lambert, M. P., Kunisaki, Y., Scheiermann, C., Schiff, L., Poncz, M., Bergman, A., et al. (2014) · Nature Medicine · doi:10.1038/nm.3707 · Cited by 679
Butler, 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 678
The Placenta Is a Niche for Hematopoietic Stem Cells
Gekas, C., Dieterlen‐Lièvre, F., Orkin, S. H., & Mikkola, H. K. A. (2005) · Developmental Cell · doi:10.1016/j.devcel.2004.12.016 · Cited by 664
Hooper, 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 662
Zhao, M. L., Perry, J. M., Marshall, H. M., Venkatraman, A., Qian, P., He, X., Ahamed, J., & Li, L. (2014) · Nature Medicine · doi:10.1038/nm.3706 · Cited by 649
Gremlin 1 Identifies a Skeletal Stem Cell with Bone, Cartilage, and Reticular Stromal Potential
Worthley, D. L., Churchill, M., Compton, J. T., Tailor, Y. H., Rao, M., Si, Y., Levin, D. E., Schwartz, M. G., Uygur, A., Hayakawa, Y., et al. (2015) · Cell · doi:10.1016/j.cell.2014.11.042 · Cited by 645
Ikuta, K., & Weissman, I. L. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.4.1502 · Cited by 637
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 637
Bruijn, M. F. T. R. D., Speck, N. A., Peeters, M. C. E., & Dzierzak, E. A. (2000) · The EMBO Journal · doi:10.1093/emboj/19.11.2465 · Cited by 637
Bone Marrow Transplantation for Sickle Cell Disease
Walters, M. C., Patience, M., Leisenring, W. M., Eckman, J. R., Scott, J. P., Mentzer, W. C., Davies, S. C., Ohene‐Frempong, K., Bernaudin, F., Matthews, D. C., et al. (1996) · New England Journal of Medicine · doi:10.1056/nejm199608083350601 · Cited by 623
Exit from dormancy provokes DNA-damage-induced attrition in haematopoietic stem cells
Walter, D., Lier, A., Geiselhart, A., Thalheimer, F. B., Huntscha, S., Sobotta, M. C., Moehrle, B., Brocks, D., Bayindir, I., Kaschutnig, P., et al. (2015) · Nature · doi:10.1038/nature14131 · Cited by 619
The journey of developing hematopoietic stem cells
Mikkola, H. K. A., & Orkin, S. H. (2006) · Development · doi:10.1242/dev.02568 · Cited by 616
Schepers, 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
The purification and characterization of fetal liver hematopoietic stem cells
Morrison, S. J., Hemmati, H. D., Wandycz, A. M., & Weissman, I. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.22.10302 · Cited by 611
Self-citationCopeland, N. G., Gilbert, D. J., Cho, B. C., Donovan, P. J., Jenkins, N. A., Cosman, D. J., Anderson, D. M., Lyman, S. D., & Williams, D. E. (1990) · Cell · doi:10.1016/0092-8674(90)90298-s · Cited by 604
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 600
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
In vivo imaging of Treg cells providing immune privilege to the haematopoietic stem-cell niche
Fujisaki, J., Wu, J. W., Carlson, A. L., Silberstein, L., Putheti, P., Larocca, R. A., Gao, W., Saito, T. I., Celso, C. L., Tsuyuzaki, H., et al. (2011) · Nature · doi:10.1038/nature10160 · Cited by 570
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
Neuroepithelial Cells Supply an Initial Transient Wave of MSC Differentiation
Takashima, Y., Era, T., Nakao, K., Kondo, S., Kasuga, M., Smith, A. G., & Nishikawa, S.-I. (2007) · Cell · doi:10.1016/j.cell.2007.04.028 · Cited by 521
Yue, R., Zhou, B. O., Shimada, I. S., Zhao, Z., & Morrison, S. J. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.02.015 · Cited by 495
Self-citationCheng, C., Adams, G. B., Perin, L., Wei, M., Zhou, X., Lam, B. S., Sacco, S. D., Mirisola, M. G., Quinn, D. I., Dorff, T. B., et al. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.04.014 · Cited by 491
Age-dependent modulation of vascular niches for haematopoietic stem cells
Kusumbe, A. P., Ramasamy, S. K., Itkin, T., Mäe, M. A., Langen, U. H., Betsholtz, C., Lapidot, T., & Adams, R. H. (2016) · Nature · doi:10.1038/nature17638 · Cited by 474
Zou, L., Barnett, B. G., Safah, H. F., LaRussa, V. F., Evdemon-Hogan, M., Mottram, P. J., Wei, S., David, O., Curiel, T. J., & Zou, W. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-1987 · Cited by 466
Differential cytokine contributions of perivascular haematopoietic stem cell niches
Asada, N., Kunisaki, Y., Pierce, H., Wang, Z., Fernandez, N., Birbrair, A., Ma’ayan, A., & Frenette, P. S. (2017) · Nature Cell Biology · doi:10.1038/ncb3475 · Cited by 453
Mizoguchi, T., Pinho, S., Ahmed, J. U., Kunisaki, Y., Hanoun, M., Mendelson, A., Ono, N., Kronenberg, H. M., & Frenette, P. S. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.03.013 · Cited by 451
Neuropathy of haematopoietic stem cell niche is essential for myeloproliferative neoplasms
Arranz, L., Sánchez-Aguilera, A., Martín-Pérez, D., Isern, J., Langa, X., Tzankov, A., Lundberg, P., Muntión, S., Tzeng, Y.-S., Lai, D.-M., et al. (2014) · Nature · doi:10.1038/nature13383 · Cited by 444
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
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
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
A subset of chondrogenic cells provides early mesenchymal progenitors in growing bones
Ono, N., Ono, W., Nagasawa, T., & Kronenberg, H. M. (2014) · Nature Cell Biology · doi:10.1038/ncb3067 · Cited by 418
Diverse and heritable lineage imprinting of early haematopoietic progenitors
Naik, S. H., Perié, L., Swart, E., Gerlach, C., van Rooij, N., de Boer, R. J., & Schumacher, T. N. (2013) · Nature · doi:10.1038/nature12013 · Cited by 416
Oestrogen increases haematopoietic stem-cell self-renewal in females and during pregnancy
Nakada, D., Oguro, H., Levi, B. P., Ryan, N., Kitano, A., Saitoh, Y., Takeichi, M., Wendt, G. R., & Morrison, S. J. (2014) · Nature · doi:10.1038/nature12932 · Cited by 409
Self-citationCXCR4 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
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
Bianco, P., & Robey, P. G. (2015) · Development · doi:10.1242/dev.102210 · Cited by 402
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
Hanoun, M., Zhang, D., Mizoguchi, T., Pinho, S., Pierce, H., Kunisaki, Y., Lacombe, J., Armstrong, S. A., Dührsen, U., & Frenette, P. S. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.06.020 · Cited by 381
Hematopoietic Stem Cells Are the Major Source of Multilineage Hematopoiesis in Adult Animals
Sawai, C. M., Babovic, S., Upadhaya, S., Knapp, D. J. H. F., Lavin, Y., Lau, C. M., Goloborodko, A., Feng, J., Fujisaki, J., Ding, L., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.08.007 · Cited by 381
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
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
β-Catenin Is Dispensable for Hematopoiesis and Lymphopoiesis
Cobas, M., Wilson, A., Ernst, B., Mancini, S. J. C., MacDonald, H. R., Kemler, R., & Radtke, F. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031615 · Cited by 358
Zhang, B., Ho, Y., Huang, Q., Maeda, T., Lin, A., Lee, S.-U., Hair, A., Holyoake, T. L., Huettner, C. S., & Bhatia, R. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.02.018 · Cited by 357
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 354
Sitnicka, E., Lin, N., Priestley, G. V., Fox, N., Broudy, V., Wolf, N., & Kaushansky, K. (1996) · Blood · doi:10.1182/blood.v87.12.4998.bloodjournal87124998 · Cited by 350
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
Zambetti, N. A., Ping, Z., Chen, S., Kenswil, K. J. G., Mylona, M. A., Sanders, M. A., Hoogenboezem, R. M., Bindels, E. M. J., Adisty, M. N., Van Strien, P. M. H., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.08.021 · Cited by 342
Christopher, M. J., Rao, M., Liu, F., Woloszynek, J. R., & Link, D. C. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20101700 · Cited by 330
Rhodes, K. E., Gekas, C., Wang, Y., Lux, C. T., Francis, C. S., Chan, D. N., Conway, S. J., Orkin, S. H., Yöder, M. C., & Mikkola, H. K. A. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.01.001 · Cited by 327
TGF-β as a candidate bone marrow niche signal to induce hematopoietic stem cell hibernation
Yamazaki, S., Iwama, A., Takayanagi, S., Eto, K., Ema, H., & Nakauchi, H. (2008) · Blood · doi:10.1182/blood-2008-04-146480 · Cited by 327
Ito, K., Turcotte, R., Cui, J., Zimmerman, S. E., Pinho, S., Mizoguchi, T., Arai, F., Runnels, J. M., Alt, C., Teruya‐Feldstein, J., et al. (2016) · Science · doi:10.1126/science.aaf5530 · Cited by 326
Isern, J., García‐García, A., MARTIN, A., Arranz, L., Martín-Pérez, D., Torroja, C., Sánchez‐Cabo, F., & Méndez‐Ferrer, S. (2014) · eLife · doi:10.7554/elife.03696 · Cited by 323
Thrombopoietin, the Mp1 ligand, is essential for full megakaryocyte development.
Kaushansky, K., Broudy, V. C., Lin, N., Jorgensen, M. J., McCarty, J. M., Fox, N., Zucker-Franklin, D., & Lofton–Day, C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.8.3234 · Cited by 313
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 313
Noncanonical 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 306
Koch, C. A., Li, C., Mesa, R. A., & Tefferi, A. (2003) · Mayo Clinic Proceedings · doi:10.4065/78.10.1223 · Cited by 302
Jenq, R. R., & van den Brink, M. R. M. (2010) · Nature reviews. Cancer · doi:10.1038/nrc2804 · Cited by 301
Chemotherapy-induced bone marrow nerve injury impairs hematopoietic regeneration
Lucas, D., Scheiermann, C., Chow, A. T., Kunisaki, Y., Bruns, I., Barrick, C. A., Tessarollo, L., & Frenette, P. S. (2013) · Nature Medicine · doi:10.1038/nm.3155 · Cited by 300
Sungaran, R., Markovic, B., & Chong, B. H. (1997) · Blood · doi:10.1182/blood.v89.1.101 · Cited by 290
Regulation of SDF-1 (CXCL12) production by osteoblasts; a possible mechanism for stem cell homing
Jung, Y., Wang, J., Schneider, A., Sun, Y., Koh-Paige, A. J., Osman, N. I., McCauley, L. K., & Taichman, R. S. (2005) · Bone · doi:10.1016/j.bone.2005.10.003 · Cited by 290
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
A perisinusoidal niche for extramedullary haematopoiesis in the spleen
Inra, C. N., Zhou, B. O., Acar, M., Murphy, M. M., Richardson, J. A., Zhao, Z., & Morrison, S. J. (2015) · Nature · doi:10.1038/nature15530 · Cited by 282
Self-citationTzeng, 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
Angiogenesis in myelodysplastic syndromes
Pruneri, G., Bertolini, F., Soligo, D. A., Carboni, N., Cortelezzi, A., Ferrucci, P. F., Buffa, R., Lambertenghi‐Deliliers, G., & Pezzella, F. (1999) · British Journal of Cancer · doi:10.1038/sj.bjc.6693515 · Cited by 268
Fetal liver hematopoietic stem cell niches associate with portal vessels
Khan, J. A., Mendelson, A., Kunisaki, Y., Birbrair, A., Kou, Y., Estape, A. A., Pinho, S., Ciero, P., Nakahara, F., Ma’ayan, A., et al. (2015) · Science · doi:10.1126/science.aad0084 · Cited by 260
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
Foxc1 is a critical regulator of haematopoietic stem/progenitor cell niche formation
Omatsu, Y., Seike, M., Sugiyama, T., Kume, T., & Nagasawa, T. (2014) · Nature · doi:10.1038/nature13071 · Cited by 254
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
Self-citationLive imaging of emerging hematopoietic stem cells and early thymus colonization
Kissa, K., Murayama, E., Zapata, A. G., Cortés, A., Perret, E., Machu, C., & Herbomel, P. (2007) · Blood · doi:10.1182/blood-2007-07-099499 · Cited by 242
Bernad, A., Kopf, M., Kulbacki, R., Weich, N., Koehler, G., & Gutiérrez-Ramos, J. (1994) · Immunity · doi:10.1016/s1074-7613(94)80014-6 · Cited by 242
Osteoclasts 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 239
Becker, R. P., & Bruyn, P. P. H. D. (1976) · American Journal of Anatomy · doi:10.1002/aja.1001450204 · Cited by 233
Ludin, A., Itkin, T., Gur‐Cohen, S., Mildner, A., Shezen, E., Golan, K., Kollet, Ó., Kalinkovich, A., Porat, Z., D’Uva, G., et al. (2012) · Nature Immunology · doi:10.1038/ni.2408 · Cited by 218
Simultaneous loss of β- and γ-catenin does not perturb hematopoiesis or lymphopoiesis
Koch, U., Wilson, A., Cobas, M., Kemler, R., MacDonald, H. R., & Radtke, F. (2007) · Blood · doi:10.1182/blood-2007-07-099754 · Cited by 204
Fgd5 identifies hematopoietic stem cells in the murine bone marrow
Gazit, R., Mandal, P. K., Ebina, W., Ben‐Zvi, A., Nombela‐Arrieta, C., Silberstein, L. E., & Rossi, D. J. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20130428 · Cited by 201
Bittencourt, H. N. D. S., Rocha, V., Chevret, S., Socié, G., Espérou, H., Devergié, A., Cortivo, L. D., Marolleau, J., Garnier, F., Ribaud, P., et al. (2002) · Blood · doi:10.1182/blood.v99.8.2726 · Cited by 198
Goncalves, K. A., Silberstein, L., Li, S., Sévère, N., Hu, M. G., Yang, H., Scadden, D. T., & Hu, G. (2016) · Cell · doi:10.1016/j.cell.2016.06.042 · Cited by 195
Burberry, A., Zeng, M. Y., Ding, L., Wicks, I. P., Inohara, N., Morrison, S. J., & Núñez, G. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.05.004 · Cited by 194
Self-citationGenetic treatment of a molecular disorder: gene therapy approaches to sickle cell disease
Hoban, M. D., Orkin, S. H., & Bauer, D. E. (2016) · Blood · doi:10.1182/blood-2015-09-618587 · Cited by 194
Ono, N., Ono, W., Mizoguchi, T., Nagasawa, T., Frenette, P. S., & Kronenberg, H. M. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.03.014 · Cited by 190
Chromothriptic Cure of WHIM Syndrome
McDermott, D. H., Gao, J., Liu, Q., Siwicki, M. R., Martens, C., Jacobs, P., Velez, D. S., Yim, E., Bryke, C. R., Hsu, N. Y.-H., et al. (2015) · Cell · doi:10.1016/j.cell.2015.01.014 · Cited by 190
Depleting dietary valine permits nonmyeloablative mouse hematopoietic stem cell transplantation
Taya, Y., Ota, Y., Wilkinson, A. C., Kanazawa, A., Watarai, H., Kasai, M., Nakauchi, H., & Yamazaki, S. (2016) · Science · doi:10.1126/science.aag3145 · Cited by 189
Zhou, B. O., Ding, L., & Morrison, S. J. (2015) · eLife · doi:10.7554/elife.05521 · Cited by 188
Self-citationWang, L., Zhang, H., Rodriguez, S., Cao, L., Parish, J., Mumaw, C., Zollman, A., Kamoka, M. M., Mu, J., Chen, D. Z., et al. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.04.021 · Cited by 186
Macrophages retain hematopoietic stem cells in the spleen via VCAM-1
Dutta, P., Hoyer, F. F., Grigoryeva, L. S., Sager, H. B., Leuschner, F., Courties, G., Borodovsky, A., Novobrantseva, T., Ruda, V. M., Fitzgerald, K., et al. (2015) · Journal of Experimental Medicine · doi:10.1084/jem.20141642 · Cited by 180
The innervation of the bone marrow in laboratory animals
CALVO, W. (1968) · American Journal of Anatomy · doi:10.1002/aja.1001230206 · Cited by 179
Hur, J., Choi, J.-I., Lee, H., Nham, P., Kim, T., Chae, C.-W., Yun, J.-Y., Kang, J.-A., Kang, J., Lee, S. E., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.01.013 · Cited by 177
Fleischman, R. A., & Mintz, B. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.11.5736 · Cited by 174
Silberstein, L., Goncalves, K. A., Kharchenko, P. V., Turcotte, R., Kfoury, Y. S., Mercier, F., Baryawno, N., Sévère, N., Bachand, J., Spencer, J. A., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.07.004 · Cited by 159
Yamazaki, K., & Allen, T. (1990) · American Journal of Anatomy · doi:10.1002/aja.1001870306 · Cited by 151
Notch2 governs the rate of generation of mouse long- and short-term repopulating stem cells
Varnum‐Finney, B., Halasz, L. M., Sun, M., Gridley, T., Radtke, F., & Bernstein, I. D. (2011) · Journal of Clinical Investigation · doi:10.1172/jci43868 · Cited by 138
Benign extramedullary myeloid proliferations
O’Malley, D. P. (2007) · Modern Pathology · doi:10.1038/modpathol.3800768 · Cited by 136
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
Bowers, M., Zhang, B., Ho, Y., Agarwal, P., Chen, C., & Bhatia, R. (2015) · Blood · doi:10.1182/blood-2014-06-582924 · Cited by 131
BMP4 regulates the hematopoietic stem cell niche
Goldman, D. C., Bailey, A. S., Pfaffle, D. L., Masri, A. A., Christian, J. L., & Fleming, W. (2009) · Blood · doi:10.1182/blood-2009-02-206433 · Cited by 129
Itkin, T., Ludin, A., Gradus, B., Gur‐Cohen, S., Kalinkovich, A., Schajnovitz, A., Ovadya, Y., Kollet, Ó., Canaani, J., Shezen, E., et al. (2012) · Blood · doi:10.1182/blood-2011-11-394692 · Cited by 123
Notch signaling distinguishes 2 waves of definitive hematopoiesis in the zebrafish embryo
Bertrand, J. Y., Schwedler, J. L., Stachura, D. L., & Traver, D. J. (2010) · Blood · doi:10.1182/blood-2009-09-244590 · Cited by 123
Primitive macrophages control HSPC mobilization and definitive haematopoiesis
Travnickova, J., Chau, V. T., Julien, E., Mateos-Langerak, J., Gonzalez, C., Lelièvre, E., Lutfalla, G., Tavian, M., & Kissa, K. (2015) · Nature Communications · doi:10.1038/ncomms7227 · Cited by 119
BMP signalling differentially regulates distinct haematopoietic stem cell types
Crisan, M., Kartalaei, P. S., Vink, C. S., Yamada-Inagawa, T., Bollérot, K., van IJcken, W. F. J., van der Linden, R., Lopes, S. M. C. D. S., Monteiro, R. M., Mummery, C. L., et al. (2015) · Nature Communications · doi:10.1038/ncomms9040 · Cited by 99
Zheng, J., Huynh, H., Umikawa, M., Silvany, R. E., & Zhang, C. C. (2010) · Blood · doi:10.1182/blood-2010-06-291716 · Cited by 95
Dissecting the Hematopoietic Microenvironment
Wolf, N. S. (1978) · Cell Proliferation · doi:10.1111/j.1365-2184.1978.tb00806.x · Cited by 94
Sl/Sld hematopoietic progenitors are deficient in situ.
Barker, J. E. (1994) · PubMed · Cited by 93
Localization of megakaryocytes in the bone marrow.
Tavassoli, M., & Aoki, M. (1989) · PubMed · Cited by 86
Sun, M., Yetman, M. J., Lee, T., Chen, Y., & Jankowsky, J. L. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23497 · Cited by 86
FGF signaling facilitates postinjury recovery of mouse hematopoietic system
Zhao, M. L., Ross, J. T., Itkin, T., Perry, J. M., Venkatraman, A., Haug, J. S., Hembree, M. J., Deng, C., Lapidot, T., He, X. C., et al. (2012) · Blood · doi:10.1182/blood-2011-11-393991 · Cited by 86
Origins and Properties of Dental, Thymic, and Bone Marrow Mesenchymal Cells and Their Stem Cells
Komada, Y., Yamane, T., Kadota, D., Isono, K., Takakura, N., Hayashi, S., & Yamazaki, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046436 · Cited by 83
Mohty, M., Duarte, R. F., Croockewit, S., Hübel, K., Kvalheim, G., & Russell, N. H. (2011) · Leukemia · doi:10.1038/leu.2010.224 · Cited by 75
Barker, J. E. (1997) · PubMed · Cited by 58
Pleiotrophin mediates hematopoietic regeneration via activation of RAS
Himburg, H. A., Yan, X., Doan, P. L., Quarmyne, M., Micewicz, E., McBride, W. H., Chao, N. J. A., Slamon, D. J., & Chute, J. P. (2014) · Journal of Clinical Investigation · doi:10.1172/jci76838 · Cited by 58
tfec controls the hematopoietic stem cell vascular niche during zebrafish embryogenesis
Mahony, C. B., Fish, R. J., Pasche, C., & Bertrand, J. Y. (2016) · Blood · doi:10.1182/blood-2016-04-710137 · Cited by 58
Singbrant, S., Karlsson, G., Ehinger, M., Olsson, K., Jaako, P., Miharada, K., Stadtfeld, M., Graf, T., & Karlsson, S. (2010) · Blood · doi:10.1182/blood-2009-05-220988 · Cited by 56
Fish to Learn: Insights into Blood Development and Blood Disorders from Zebrafish Hematopoiesis
Avagyan, S., & Zon, L. I. (2016) · Human Gene Therapy · doi:10.1089/hum.2016.024 · Cited by 53
Distinctive Mesenchymal-Parenchymal Cell Pairings Govern B Cell Differentiation in the Bone Marrow
Yu, V. W. C., Lymperi, S., Oki, T., Jones, A., Swiatek, P., Vasic, R., Ferraro, F., & Scadden, D. T. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.06.009 · Cited by 52
Smith‐Berdan, S., Nguyen, A., Hong, M. A., & Forsberg, E. C. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.12.013 · Cited by 47
Lai, C., Yamazaki, S., Okabe, M., Suzuki, S., Maeyama, Y., Iimura, Y., Onodera, M., Kakuta, S., Iwakura, Y., Nojima, M., et al. (2014) · Stem Cells · doi:10.1002/stem.1670 · Cited by 43
Measurement of megakaryocyte frequency and ploidy distribution in unfractionated murine bone marrow.
Corash, L., Levin, J., Mok, Y., Baker, G., & McDowell, J. R. (1989) · PubMed · Cited by 40
Myocardial Extramedullary Hematopoiesis: A Clinicopathologic Study
Hill, D. A., & Swanson, P. E. (2000) · Modern Pathology · doi:10.1038/modpathol.3880135 · Cited by 37
Tajima, Y., Ito, K., Umino, A., Wilkinson, A. C., Nakauchi, H., & Yamazaki, S. (2017) · Scientific Reports · doi:10.1038/srep40684 · Cited by 23
Johns, J. L., & Borjesson, D. (2011) · Innate Immunity · doi:10.1177/1753425911413794 · Cited by 18
Quantitative trait gene Slit2 positively regulates murine hematopoietic stem cell numbers
Waterstrat, A., Rector, K., Geiger, H., & Liang, Y. (2016) · Scientific Reports · doi:10.1038/srep31412 · Cited by 9
Flagged first, then by citations
Cited by
Sorted by citations
Zhao, Z., Chen, X., Dowbaj, A. M., Sljukic, A., Bratlie, K., Lin, L., Fong, E. L. S., Balachander, G. M., Chen, Z., Soragni, A., et al. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00174-y · Cited by 1,082
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
Buenrostro, J. D., Corces, M. R., Lareau, C. A., Wu, B., Schep, A. N., Aryee, M. J., Majeti, R., Chang, H. Y., & Greenleaf, W. J. (2018) · Cell · doi:10.1016/j.cell.2018.03.074 · Cited by 670
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 562
Menstruation: science and society
Critchley, H., Babayev, E., Bulun, S. E., Clark, S., Garcia-Grau, I., Gregersen, P. K., Kilcoyne, A., Kim, J.-Y. J., Lavender, M. D., Marsh, E. E., et al. (2020) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2020.06.004 · Cited by 533
Metadata
- Authors
- Crane, G. M., Jeffery, E., & Morrison, S. J.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Morrison, Sean J.
- Venue
- Nature Reviews Immunology
- Published
- 2017-06-12
- Volume
- 17
- Issue
- 9
- Pages
- 573-590
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W2624346565
- Cited by
- 712
- References
- 185
- Citations by year
- 2026: 30 · 2025: 41 · 2024: 75 · 2023: 68 · 2022: 79 · 2021: 133 · 2020: 103 · 2019: 78 · 2018: 86 · 2017: 17
- FWCI
- 12.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Keywords
- hematopoietic stem cells, stem cell niche, bone marrow, spleen, perivascular niche, niche cells, endothelial cells, mesenchymal stem cells, niche factors, HSC maintenance
- MeSH terms
- Adult, Bone Marrow, Hematopoiesis, Hematopoietic Stem Cells, Humans, Spleen, Leukopoiesis, Adult Stem Cells, Stem Cell Niche
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