The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Fundamental properties of unperturbed haematopoiesis from stem cells in vivo
Abstract
Haematopoietic stem cells (HSCs) are widely studied by HSC transplantation into immune- and blood-cell-depleted recipients. Single HSCs can rebuild the system after transplantation. Chromosomal marking, viral integration and barcoding of transplanted HSCs suggest that very low numbers of HSCs perpetuate a continuous stream of differentiating cells. However, the numbers of productive HSCs during normal haematopoiesis, and the flux of differentiating progeny remain unknown. Here we devise a mouse model allowing inducible genetic labelling of the most primitive Tie2(+) HSCs in bone marrow, and quantify label progression along haematopoietic development by limiting dilution analysis and data-driven modelling. During maintenance of the haematopoietic system, at least 30% or ∼5,000 HSCs are productive in the adult mouse after label induction. However, the time to approach equilibrium between labelled HSCs and their progeny is surprisingly long, a time scale that would exceed the mouse's life. Indeed, we find that adult haematopoiesis is largely sustained by previously designated 'short-term' stem cells downstream of HSCs that nearly fully self-renew, and receive rare but polyclonal HSC input. By contrast, in fetal and early postnatal life, HSCs are rapidly used to establish the immune and blood system. In the adult mouse, 5-fluoruracil-induced leukopenia enhances the output of HSCs and of downstream compartments, thus accelerating haematopoietic flux. Label tracing also identifies a strong lineage bias in adult mice, with several-hundred-fold larger myeloid than lymphoid output, which is only marginally accentuated with age. Finally, we show that transplantation imposes severe constraints on HSC engraftment, consistent with the previously observed oligoclonal HSC activity under these conditions. Thus, we uncover fundamental differences between the normal maintenance of the haematopoietic system, its regulation by challenge, and its re-establishment after transplantation. HSC fate mapping and its linked modelling provide a quantitative framework for studying in situ the regulation of haematopoiesis in health and disease.
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
“However, barcodes produced through Cre-lox recombination in different hematopoietic cells confirmed a major replicative role of MPPs, while also demonstrating a consistent contribution of HSCs (Busch et al., 2015).”
From Unraveling Hematopoiesis through the Lens of Genomics (2020) · cites this paper as Busch et al., 2015
Citations
Cites
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
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors
Gomez Perdiguero, E., Klapproth, K., Schulz, C., Busch, K., Azzoni, E., Crozet, L., Garner, H., Trouillet, C., de Bruijn, M. F., Geissmann, F., et al. (2015) · Nature · doi:10.1038/nature13989 · Cited by 2,339 · cited 1×
“8, 4) day (21), bCMP 5 4 (21, 4) day(21), bCLP 5 3 (0.”
Self-citationLong-Term Lymphohematopoietic Reconstitution by a Single CD34-Low/Negative Hematopoietic Stem Cell
Osawa, M., Hanada, K., Hamada, H., & Nakauchi, H. (1996) · Science · doi:10.1126/science.273.5272.242 · Cited by 2,141
Wilson, 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
Weissman, I. L. (2000) · Cell · doi:10.1016/s0092-8674(00)81692-x · Cited by 1,827
Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation
Sato, T. N., Tozawa, Y., Deutsch, U., Wolburg‐Buchholz, K., Fujiwara, Y., Gendron‐Maguire, M., Gridley, T., Wolburg, H., Risau, W., & Qin, Y. (1995) · Nature · doi:10.1038/376070a0 · Cited by 1,821
Schwenk, F., Baron, U., & Rajewsky, K. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.24.5080 · Cited by 1,289
Dumont, D. J., Gradwohl, G., Fong, G. H., Puri, M. C., Gertsenstein, M., Auerbach, A., & Breitman, M. L. (1994) · Genes & Development · doi:10.1101/gad.8.16.1897 · Cited by 985
Developmental potential and dynamic behavior of hematopoietic stem cells
Lemischka, I. R., Raulet, D. H., & Mulligan, R. C. (1986) · Cell · doi:10.1016/0092-8674(86)90566-0 · Cited by 848
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 753
To B1a or not to B1a: do hematopoietic stem cells contribute to tissue-resident immune cells?
Beaudin, A. E., & Forsberg, E. C. (2016) · Blood · doi:10.1182/blood-2016-10-697813 · Cited by 26
Tian, S., Huang, P., Gu, Y., Yang, J., Wu, R., Zhao, J., Liu, A., & Zhang, W. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00408 · Cited by 22
To portray clonal evolution in blood cancer, count your stem cells
Lyne, A.-M., Laplane, L., & Perié, L. (2020) · Blood · doi:10.1182/blood.2020008407 · Cited by 26
Stem Cells, Hematopoiesis and Lineage Tracing: Transplantation-Centric Views and Beyond
Konturek-Cieśla, A., & Bryder, D. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.903528 · Cited by 24
Sarkaria, S. M., Decker, M., & Ding, L. (2018) · BioEssays · doi:10.1002/bies.201700190 · Cited by 22
Zhao, H., & Deininger, M. W. (2023) · Blood · doi:10.1182/blood.2022017152 · Cited by 21
Cancer as a Disease of Development Gone Awry
Stanger, B. Z., & Wahl, G. M. (2023) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-031621-025610 · Cited by 23
Stem cell heterogeneity, plasticity, and regulation
Cui, Z., Wei, H., Goding, C. R., & Cui, R. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122240 · Cited by 21
Singh, A., Chia, J. J., Rao, D. S., & Hoffmann, A. (2025) · Blood · doi:10.1182/blood.2024025598 · Cited by 21
How hematopoietic stem/progenitors and their niche sense and respond to infectious stress
Kobayashi, H., Suda, T., & Takubo, K. (2015) · Experimental Hematology · doi:10.1016/j.exphem.2015.11.008 · Cited by 21
MicroRNAs in Control of Stem Cells in Normal and Malignant Hematopoiesis
Roden, C., & Lü, J. (2016) · Current Stem Cell Reports · doi:10.1007/s40778-016-0057-1 · Cited by 23
Retracing the in vivo haematopoietic tree using single‐cell methods
Perié, L., & Duffy, K. R. (2016) · FEBS Letters · doi:10.1002/1873-3468.12299 · Cited by 27
Vainieri, M. L., Blagborough, A. M., MacLean, A. L., Haltalli, M. L. R., Ruivo, N., Fletcher, H. A., Stumpf, M. P. H., Sinden, R. E., & Celso, C. L. (2016) · Open Biology · doi:10.1098/rsob.160038 · Cited by 22
Hoxb5 defines the heterogeneity of self-renewal capacity in the hematopoietic stem cell compartment
Sakamaki, T., Kao, K. S., Nishi, K., Chen, J. Y., Sadaoka, K., Fujii, M., Takaori‐Kondo, A., Weissman, I. L., & Miyanishi, M. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.12.077 · Cited by 21
Marchetti, F., Zhou, G., LeBlanc, D. P. M., White, P. A., Williams, A., Yauk, C. L., & Douglas, G. R. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-02977-6 · Cited by 21
Takahashi, M., Barile, M., Chapple, R. H., Tseng, Y.-J., Nakada, D., Busch, K., Fanti, A.-K., Säwén, P., Bryder, D., Höfer, T., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.02.020 · Cited by 21
Self-citationHematopoietic Stem Cells Self-Renew Symmetrically or Gradually Proceed to DifferentiationPreprint
Barile, M., Busch, K., Fanti, A.-K., Greco, A., Wang, X., Oguro, H., Zhang, Q., Morrison, S. J., Rodewald, H.-R., & Höfer, T. (2020) · SSRN Electronic Journal · doi:10.1101/2020.08.06.239186 · Cited by 24
Self-citationNew frameworks for hematopoiesis derived from single-cell genomics
Safina, K. R., & van Galen, P. (2024) · Blood · doi:10.1182/blood.2024024006 · Cited by 23
Mou, R., Ma, J., Ju, X., Wu, Y., Chen, Q., Li, J., Shang, T., Chen, S., Yang, Y., Li, Y., et al. (2024) · Cell Stem Cell · doi:10.1016/j.stem.2024.09.018 · Cited by 20
Xu, Y., Murphy, A. J., & Fleetwood, A. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042234 · Cited by 23
HSC Niche Dynamics in Regeneration, Pre-malignancy, and Cancer: Insights From Mathematical Modeling
Pedersen, R. K., Andersen, M., Skov, V., Kjær, L., Hasselbalch, H. C., Ottesen, J. T., & Stiehl, T. (2022) · Stem Cells · doi:10.1093/stmcls/sxac079 · Cited by 20
Srinivasan, J., Vasudev, A., Shasha, C., Selden, H. J., Perez, E., LaFleur, B., Sinari, S. A., Krueger, A., Richie, E. R., & Ehrlich, L. I. R. (2023) · Aging Cell · doi:10.1111/acel.13870 · Cited by 23
Hou, Y., Sheng, Z., Mao, X., Li, C., Chen, J., Zhang, J., Huang, H., Ruan, H., Luo, L., & Li, L. (2016) · Scientific Reports · doi:10.1038/srep36853 · Cited by 21
Radtke, S., Enstrom, M., Pande, D., Duke, E. R., Ojeda, E. F. C., Madhu, R., Owen, S., Kanestrom, G., Cui, M., Perez, A. M., et al. (2023) · Blood · doi:10.1182/blood.2022018564 · Cited by 19
Bidirectional interplay between metabolism and epigenetics in hematopoietic stem cells and leukemia
Zhang, Y. W., Schönberger, K., & Cabezas‐Wallscheid, N. (2023) · The EMBO Journal · doi:10.15252/embj.2022112348 · Cited by 24
Decoding early myelopoiesis from dynamics of core endogenous network
Su, H., Wang, G., Yuan, R., Wang, J., Tang, Y., Ao, P., & Zhu, X. (2017) · Science China Life Sciences · doi:10.1007/s11427-017-9059-y · Cited by 19
Epigenetic Control of Haematopoietic Stem Cell Aging and Its Clinical Implications
Choudry, F., & Frontini, M. (2015) · Stem Cells International · doi:10.1155/2016/5797521 · Cited by 19
Stem cell homeostasis by integral feedback through the niche
Becker, N. B., Günther, M., Li, C., Jolly, A., & Höfer, T. (2018) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2018.12.029 · Cited by 19
Self-citationThe bone marrow hematopoietic niche and its adaptation to infection
Gomes, A. C., Saraiva, M., & Gomes, M. S. (2021) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2020.05.014 · Cited by 18
Kim, E., Cheng, Y., Bolton-Gillespie, E., Cai, X., Ma, C., Tarangelo, A., Le, L., Jambhekar, M., Raman, P., Hayer, K. E., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20160719 · Cited by 18
Molecular and cellular bases of trained immunity
Sun, S. J., Aguirre‐Gamboa, R., & Barreiro, L. B. (2026) · Immunity · doi:10.1016/j.immuni.2026.03.001 · Cited by 18
The slippery slope of hematopoietic stem cell aging
Wahlestedt, M., & Bryder, D. (2017) · Experimental Hematology · doi:10.1016/j.exphem.2017.09.008 · Cited by 18
Watanuki, S., Kobayashi, H., Sugiura, Y., Yamamoto, M., Karigane, D., Shiroshita, K., Sorimachi, Y., Fujita, S., Morikawa, T., Koide, S., et al. (2023) · eLife · doi:10.7554/elife.87674 · Cited by 19
Jani, P. K., Petkau, G., Kawano, Y., Klemm, U., Guerra, G. M., Heinz, G. A., Heinrich, F., Durek, P., Mashreghi, M., & Melchers, F. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002015 · Cited by 18
Tseng, Y.-J., Kageyama, Y., Murdaugh, R. L., Kitano, A., Kim, J. H., Hoegenauer, K. A., Tiessen, J., Smith, M. H., Uryu, H., Takahashi, K., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-44718-0 · Cited by 21
Mechanisms underlying the heterogeneity of myelodysplastic syndromes
Dussiau, C., & Fontenay, M. (2017) · Experimental Hematology · doi:10.1016/j.exphem.2017.10.004 · Cited by 19
Klose, M., Florian, M. C., Gerbaulet, A., Geiger, H., & Glauche, I. (2019) · Stem Cells · doi:10.1002/stem.3005 · Cited by 19
Tak, T., Prevedello, G., Simon, G., Paillon, N., Benlabiod, C., Marty, C., Plo, I., Duffy, K. R., & Perié, L. (2021) · eLife · doi:10.7554/elife.60624 · Cited by 18
Necroinflammation emerges as a key regulator of hematopoiesis in health and disease
Jost, P. J., & Höckendorf, U. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0194-4 · Cited by 21
Helios represses megakaryocyte priming in hematopoietic stem and progenitor cells
Cova, G., Taroni, C., Deau, M.-C., Cai, Q., Mittelheisser, V., Philipps, M., Jung, M., Cerciat, M., Le Gras, S., Thibault-Carpentier, C., et al. (2021) · Journal of Experimental Medicine · doi:10.1084/jem.20202317 · Cited by 17
Dissecting stem cell differentiation using single cell expression profiling
Moignard, V., & Göttgens, B. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.08.005 · Cited by 18
Grb2 regulates the proliferation of hematopoietic stem and progenitors cells
Frelin, C., Ofran, Y., Ruston, J., Hayun, M., Ofir, Y. D., Khier, Y., Rozales, K., Brenner, B., Iscove, N. N., Pawson, T. J., et al. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.09.018 · Cited by 18
Stem cell decoupling underlies impaired lymphoid development during aging
Jang, G., Contreras, S., Esteva, E., Upadhaya, S., Feng, J., Adams, N. M., Richard, É., Awatramani, R. B., Sawai, C. M., & Reizis, B. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2302019120 · Cited by 19
Revisiting the lineage contribution of hematopoietic stem and progenitor cells
Gao, S., Zhang, Y., & Liu, F. (2023) · Development · doi:10.1242/dev.201609 · Cited by 17
Comazzetto, S., Cassidy, D. L., DeVilbiss, A., Jeffery, E. C., Ottesen, B. R., Reyes, A. R., Paul, A., Bansal, S., Xie, S. Z.-J., Muh, S., et al. (2024) · Blood · doi:10.1182/blood.2024024769 · Cited by 17
Fotopoulou, F., Rodriguez-Correa, E., Dussiau, C., & Milsom, M. D. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104698 · Cited by 17
Output without input: the lifelong productivity of hematopoietic stem cells
Höfer, T., & Rodewald, H.-R. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.08.003 · Cited by 17
Self-citationSingle-cell fate decisions of bipotential hematopoietic progenitors
Brand, M., & Morrissey, E. R. (2020) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000592 · Cited by 19
Wnt-5A/B Signaling in Hematopoiesis throughout Life
de Rezende, M. M., Justo, G. Z., Paredes‐Gamero, E. J., & Gosens, R. (2020) · Cells · doi:10.3390/cells9081801 · Cited by 17
Tang, W., He, J., Huang, T., Bai, Z., Wang, C., Wang, H., Yang, R., Ni, Y., Hou, J. W., Wang, J., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.728057 · Cited by 17
Gao, J., Yim, E., Siwicki, M. R., Yang, A. Y., Liu, Q., Azani, A. B., Owusu-Ansah, A., McDermott, D. H., & Murphy, P. M. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120375 · Cited by 17
Slow cycling and durable Flt3+ progenitors contribute to hematopoiesis under native conditions
Solomon, M. P., Song, B., Govindarajah, V., Good, S., Arasu, A., Hinton, E. B., Thakkar, K., Bartram, J., Filippi, M., Cancelas, J. A., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20231035 · Cited by 16
Zhang, Q., Olofzon, R., Konturek-Cieśla, A., Yuan, O., & Bryder, D. (2023) · eLife · doi:10.7554/elife.91826 · Cited by 16
The heart is a resident tissue for hematopoietic stem and progenitor cells in zebrafish
Bornhorst, D., Hejjaji, A. V., Steuter, L., Woodhead, N. M., Maier, P., Gentile, A., Alhajkadour, A., Santis, O., Weber, M., Kikhi, K., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51920-7 · Cited by 16
Understanding Hematological Toxicities Using Mathematical Modeling
Fornari, C., O’Connor, L. O., Yates, J. W. T., Cheung, S. Y. A., Jodrell, D. I., Mettetal, J. T., & Collins, T. A. (2018) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.1080 · Cited by 16
Conditional Selection of B Cells in Mice With an Inducible B Cell Development
Hobeika, E., Dautzenberg, M., Levit‐Zerdoun, E., Pelanda, R., & Reth, M. G. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01806 · Cited by 16
Self-citationClonal approaches to understanding the impact of mutations on hematologic disease development
Nangalia, J., Mitchell, E., & Green, A. R. (2019) · Blood · doi:10.1182/blood-2018-11-835405 · Cited by 19
Clones assemble! The clonal complexity of blood during ontogeny and disease
Ganuza, M., Hall, T., Obeng, E. A., & McKinney‐Freeman, S. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.01.009 · Cited by 17
Loke, J. C. T., Kim, P. G., Nguyen, T. T. P., Boileau, M., McConkey, M. E., Miller, A., Shin, W., Hergott, C. A., Ericsson, M., Nordstrom, A. E. H., et al. (2025) · Blood · doi:10.1182/blood.2024028033 · Cited by 17
Jafari, A. H., Allahverdy, A., Moghaddam, A. K., Rahbar, S., Shafiekhani, S., Mirzaei, H. R., Amanpour, S., Etemadi, Y., & Hadjati, J. (2019) · Journal of Medical Signals & Sensors · doi:10.4103/jmss.jmss_33_18 · Cited by 15
Usp22 is an intracellular regulator of systemic emergency hematopoiesis
Dietlein, N., Wang, X., Metz, J., Disson, O., Shang, F., Beyersdörffer, C., Rodriguez-Correa, E., Lipka, D. B., Begus‐Nahrmann, Y., Kosinsky, R. L., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abq2061 · Cited by 15
Self-citationRoles of pyroptosis in intervertebral disc degeneration
Zhou, K., Ran, R., Gong, C.-Y., Zhang, S.-B., Ma, C.-W., Lv, J.-Y., Lei, Z.-Y., Ren, Y., & Zhang, H.-H. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154685 · Cited by 15
Kinase-inactivated CDK6 preserves the long-term functionality of adult hematopoietic stem cells
Mayer, I. M., Doma, E., Klampfl, T., Prchal‐Murphy, M., Kollmann, S., Schirripa, A., Scheiblecker, L., Zojer, M., Kunowska, N., Gebrail, L., et al. (2024) · Blood · doi:10.1182/blood.2023021985 · Cited by 16
Nilsson, A. R., Pronk, C. J., & Bryder, D. (2015) · Experimental Hematology · doi:10.1016/j.exphem.2015.05.003 · Cited by 15
Using Zebrafish to Study Pathways that Regulate Hematopoietic Stem Cell Self-Renewal and Migration
Choudhuri, A., Fast, E. M., & Zon, L. I. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.05.018 · Cited by 15
Development of the hematopoietic system: Role of inflammatory factors
Hayashi, Y., Sezaki, M., & Takizawa, H. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.341 · Cited by 16
Systems analysis of hematopoiesis using single-cell lineage tracing
Rodriguez-Fraticelli, A., & Camargo, F. D. (2020) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000624 · Cited by 16
Understanding Normal and Pathological Hematopoietic Stem Cell Biology Using Mathematical Modelling
Brunetti, M., Mackey, M. C., & Craig, M. (2021) · Current Stem Cell Reports · doi:10.1007/s40778-021-00191-9 · Cited by 17
Chavez, J. S., Rabe, J. L., Hernandez, G., Mills, T., Niño, K. E., Davizon‐Castillo, P., & Pietras, E. M. (2022) · Cells · doi:10.3390/cells11040680 · Cited by 16
Spotlighting adult stem cells: advances, pitfalls, and challenges
Altshuler, A., Wickström, S. A., & Shalom‐Feuerstein, R. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.09.007 · Cited by 15
De novo hematopoiesis from the fetal lung
Yeung, A. K., Villacorta-Martín, C., Lindstrom-Vautrin, J., Belkina, A. C., Vanuytsel, K., Dowrey, T. W., Ysasi, A. B., Bawa, P., Wang, F., Vrbanac, V. D., et al. (2023) · Blood Advances · doi:10.1182/bloodadvances.2022008347 · Cited by 15
Stem-cell dynamics and lineage topology from in vivo fate mapping in the hematopoietic system
Höfer, T., Barile, M., & Floßdorf, M. (2016) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2016.04.001 · Cited by 15
Self-citationThe chromatin-associated Sin3B protein is required for hematopoietic stem cell functions in mice
Cantor, D. J., & David, G. (2016) · Blood · doi:10.1182/blood-2016-06-721746 · Cited by 16
New genetic tools for the in vivo study of hematopoietic stem cell function
Upadhaya, S., Reizis, B., & Sawai, C. M. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.02.004 · Cited by 15
Chasing Mavericks: The quest for defining developmental waves of hematopoiesis
Cool, T., & Forsberg, E. C. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.01.001 · Cited by 16
Mayer, I. M., Hoelbl‐Kovacic, A., Sexl, V., & Doma, E. (2022) · Cancers · doi:10.3390/cancers14071723 · Cited by 18
Xu, S., Kim, S., Chen, I. S. Y., & Chou, T. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006489 · Cited by 15
Mast Cell Repopulating Ability Is Lost During the Transition From Pre-HSC to FL HSC
Yoshimoto, M., Kosters, A., Cornelius, S. A., Valiente, N., Cheng, H., Latorre, A., Nishida, C., Ghosn, E., & Kobayashi, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.896396 · Cited by 14
Layered immune system development in mice and humans
Dorshkind, K. A., & Crooks, G. M. (2023) · Immunological Reviews · doi:10.1111/imr.13198 · Cited by 14
Single-cell lineage tracing approaches to track kidney cell development and maintenance
Yoon, B., Kim, H., Jung, S. W., & Park, J. (2024) · Kidney International · doi:10.1016/j.kint.2024.01.045 · Cited by 14
Modeling human RNA spliceosome mutations in the mouse: not all mice were created equal
Xu, J. J., Smeets, M. F. M. A., Tan, S. Y., Wall, M., Purton, L. E., & Walkley, C. R. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.11.001 · Cited by 15
Specification of hematopoietic stem cells in mammalian embryos: A rare or frequent event?
Ganuza, M., Clements, W. K., & McKinney‐Freeman, S. (2021) · Blood · doi:10.1182/blood.2020009839 · Cited by 14
Emerging role of the RNA-editing enzyme ADAR1 in stem cell fate and function
Lu, D., Lu, J., Liu, Q., & Zhang, Q. (2023) · Biomarker Research · doi:10.1186/s40364-023-00503-7 · Cited by 14
How nutrition regulates hematopoietic stem cell features
Schönberger, K., & Cabezas‐Wallscheid, N. (2023) · Experimental Hematology · doi:10.1016/j.exphem.2023.09.008 · Cited by 14
The changing face of hematopoiesis: a spectrum of options is available to stem cells
Brown, G., Tsapogas, P., & Ceredig, R. (2018) · Immunology and Cell Biology · doi:10.1111/imcb.12055 · Cited by 15
Mapping Active Gene-Regulatory Regions in Human Repopulating Long-Term HSCs
Wünsche, P., Eckert, E., Holland‐Letz, T., Paruzynski, A., Hotz‐Wagenblatt, A., Fronza, R., Rath, T., Gil-Fariña, I., Schmidt, M., Kalle, C. V., et al. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.06.003 · Cited by 14
Self-citationDu, J., Jing, J., Chen, S., Yuan, Y., Feng, J., Ho, T., Sehgal, P., Xu, J., Jiang, X., & Chai, Y. (2021) · Development · doi:10.1242/dev.198838 · Cited by 14
“Hierarchy” and “Holacracy”; A Paradigm of the Hematopoietic System
Yokota, T. (2019) · Cells · doi:10.3390/cells8101138 · Cited by 14
Building bones for blood and beyond: the growing field of bone marrow niche model development
Doherty-Boyd, W. S., Donnelly, H., Tsimbouri, M. P., & Dalby, M. J. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104232 · Cited by 13
Advances in ex vivo expansion of hematopoietic stem and progenitor cells for clinical applications
Branco, A., Rayabaram, J., Miranda, C. C., Fernandes‐Platzgummer, A., Fernandes, T. G., Sajja, S., da Silva, C. L., & Vemuri, M. C. (2024) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2024.1380950 · Cited by 13
Dong, F., Zhang, S., Zhu, C., Yang, Z., Wang, L., Ma, Y., Lu, J., Li, X., Wang, X., Wang, N., et al. (2025) · Blood · doi:10.1182/blood.2024027872 · Cited by 13
Lv, H., Wang, C., Liu, Z., Quan, M., Li, K., Gou, F., Shi, X., Liu, Q., Yu, Y., Zhu, P., et al. (2025) · Circulation · doi:10.1161/circulationaha.124.069420 · Cited by 14
Fraint, E., Ulloa, B. A., Norberto, M. F., Potts, K. S., & Bowman, T. V. (2020) · Stem Cells Translational Medicine · doi:10.1002/sctm.20-0294 · Cited by 15
Repolarization of HSC attenuates HSCs failure in Shwachman–Diamond syndrome
Kumar, S., Nattamai, K., Hassan, A., Amoah, A., Karns, R. A., Zhang, C., Liang, Y., Shimamura, A., Florian, M. C., Bissels, U., et al. (2020) · Leukemia · doi:10.1038/s41375-020-01054-8 · Cited by 13
Optimal experimental design for mathematical models of haematopoiesis
Lomeli, L. M., Iniguez, A., Tata, P. V., Jena, N., Liu, Z., Etten, R. A. V., Lander, A. D., Shahbaba, B., Lowengrub, J. S., & Minin, V. N. (2021) · Journal of The Royal Society Interface · doi:10.1098/rsif.2020.0729 · Cited by 13
Lopez, A. G., Gutiérrez, F., Saavedra, L., Hebert, E. M., Alvarez, S., & Salva, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.647049 · Cited by 13
Niche Regulation of Hematopoiesis: The Environment Is “Micro,” but the Influence Is Large
Rasheed, A. (2022) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.121.316235 · Cited by 14
Yoshida, K., Satoh, Y., Uchimura, A., Misumi, M., Kyoizumi, S., Taga, M., Matsuda, Y., Noda, A., & Kusunoki, Y. (2022) · Scientific Reports · doi:10.1038/s41598-022-21621-6 · Cited by 13
Clonal analysis of stem cells in differentiation and disease
Colom, B., & Jones, P. H. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.07.002 · Cited by 13
Hematopoietic Stem Cells and RegenerationPreprint
Biermann, M., & Reya, T. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a040774 · Cited by 14
Metadata
- Authors
- Busch, K., Klapproth, K., Barile, M., Flossdorf, M., Holland-Letz, T., Schlenner, S. M., Reth, M., Höfer, T., & Rodewald, H.-R.
- Affiliations
- German Cancer Research Center (DE)
- KU Leuven (BE)
- University of Freiburg (DE)
- Corresponding author
- Höfer, Thomas
- Rodewald, Hans-Reimer
- Venue
- Nature
- Published
- 2015-02-11
- Volume
- 518
- Issue
- 7540
- Pages
- 542-546
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2142043313
- Cited by
- 769
- References
- 34
- Citations by year
- 2026: 31 · 2025: 48 · 2024: 72 · 2023: 72 · 2022: 71 · 2021: 69 · 2020: 75 · 2019: 56 · 2018: 88 · 2017: 80 · 2016: 79 · 2015: 26
- FWCI
- 71.55
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- FreiDok plus (Universitätsbibliothek Freiburg) (submittedVersion)
- Funders
- Deutsches Krebsforschungszentrum
- 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 › Hematology › Blood disorders and treatments
- Keywords
- hematopoietic stem cells, self-renewal, long-term HSCs, progenitor cells, limiting dilution analysis
- MeSH terms
- Aging, Animals, Animals, Newborn, Female, Fetus, Fluorouracil, Hematopoiesis, Hematopoietic Stem Cells, Male, Stem Cells, Bone Marrow Transplantation, Cell Lineage, Receptor, TIE-2, Cell Proliferation, Mice, Cell Tracking
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