The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Autophagy maintains the metabolism and function of young and old stem cells
Open accessAbstract
With age, haematopoietic stem cells lose their ability to regenerate the blood system, and promote disease development. Autophagy is associated with health and longevity, and is critical for protecting haematopoietic stem cells from metabolic stress. Here we show that loss of autophagy in haematopoietic stem cells causes accumulation of mitochondria and an activated metabolic state, which drives accelerated myeloid differentiation mainly through epigenetic deregulations, and impairs haematopoietic stem-cell self-renewal activity and regenerative potential. Strikingly, most haematopoietic stem cells in aged mice share these altered metabolic and functional features. However, approximately one-third of aged haematopoietic stem cells exhibit high autophagy levels and maintain a low metabolic state with robust long-term regeneration potential similar to healthy young haematopoietic stem cells. Our results demonstrate that autophagy actively suppresses haematopoietic stem-cell metabolism by clearing active, healthy mitochondria to maintain quiescence and stemness, and becomes increasingly necessary with age to preserve the regenerative capacity of old haematopoietic stem cells.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“During ageing, tissue regenerative functions decline, in part due to stem cell-intrinsic accumulation of damage (for example, DNA damage, loss of proteostasis and oxidative damage), functional decay of niche cells and increased inflammation (inflammageing)4–9 through uncharacterized mechanisms.”
From Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration (2023) · cites this paper as [7]
Experimental — accuracy not yet measuredIn the citing paper
“the functional heterogeneity of the HSC population increases with age.”
From Aging of hematopoietic stem cells (2018) · cites this paper as [33]
In the citing paper
“individual HSCs behave very differently.”
From Aging of hematopoietic stem cells (2018) · cites this paper as [33]
In the citing paper
“in aged mice that display an overall increase in HSC pool size”
From Aging of hematopoietic stem cells (2018) · cites this paper as [33]
In the citing paper
“A large fraction of aged HSCs show impaired levels of autophagy.”
From Aging of hematopoietic stem cells (2018) · cites this paper as [33]
In the citing paper
“Autophagy, which helps degrade large aggregates or damaged organelles, is critical to maintain HSCs during ageing106.”
From Ageing and rejuvenation of tissue stem cells and their niches (2023) · cites this paper as [106]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
limma powers differential expression analyses for RNA-sequencing and microarray studies
Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv007 · Cited by 40,458
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982
Bolstad, B. M., Irizarry, R. A., Åstrand, M., & Speed, T. P. (2003) · Bioinformatics · doi:10.1093/bioinformatics/19.2.185 · Cited by 8,328
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
Hara, T., Nakamura, K., Matsui, M., Yamamoto, A., Nakahara, Y., Suzuki-Migishima, R., Yokoyama, M., Mishima, K., Saito, I., Okano, H., et al. (2006) · Nature · doi:10.1038/nature04724 · Cited by 3,882
Regulation mechanisms and signaling pathways of autophagy
He, C., & Klionsky, D. J. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102808-114910 · Cited by 3,609
Autophagy in immunity and inflammation
Levine, B., Mizushima, N., & Virgin, H. W. (2011) · Nature · doi:10.1038/nature09782 · Cited by 3,289
Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273
Hematopoiesis: An Evolving Paradigm for Stem Cell Biology
Orkin, S. H., & Zon, L. I. (2008) · Cell · doi:10.1016/j.cell.2008.01.025 · Cited by 2,570
methylKit: a comprehensive R package for the analysis of genome-wide DNA methylation profiles
Akalin, A., Kormáksson, M., Li, S., Garrett-Bakelman, F. E., Figueroa, M. E., Melnick, A. M., & Mason, C. E. (2012) · Genome biology · doi:10.1186/gb-2012-13-10-r87 · Cited by 2,269
Self-citationOWEN, M. R., DORAN, E., & HALESTRAP, A. P. (2000) · Biochemical Journal · doi:10.1042/bj3480607 · Cited by 2,157
Flagged first, then by citations
Cited by
Sorted by citations
Items 701–800 of 895
Chen, F., Chen, N., Wang, L., Zeng, H., Lu, Y., Liu, Y., Chen, J., Xu, Y., Chen, M., Wang, S., et al. (2026) · HemaSphere · doi:10.1002/hem3.70334 · Cited by 2
Decline of chaperone-mediated autophagy in aging impairs macrophage clearance of senescent cells
Sereda, R., Lindenau, K. L., Díaz, A., Liu, Z., Santiago‐Fernández, O., Khawaja, R. R., Cutler, R. R., Calyeca, J., McCabe, M., Durand, S., et al. (2026) · Nature Aging · doi:10.1038/s43587-026-01240-w · Cited by 4
Human stem cells – sources, sourcing and in vitro methods
Szubarga, A., Kamińska, M., Kotlarz, W., Malewski, S., Zawada, W., Kuczma, M., Ješeta, M., & Antosik, P. (2021) · Medical Journal of Cell Biology · doi:10.2478/acb-2021-0011 · Cited by 2
Hungry Hematopoietic Stem Cells during Bacterial Infection: Fatty Acid for Food
Filippi, M. (2022) · Immunometabolism · doi:10.20900/immunometab20220011 · Cited by 2
Bmi‐1 alleviates alveolar bone resorption through the regulation of autophagy
Chu, Y., Liu, S., Yan, L., & Gong, A. (2024) · Journal of Periodontology · doi:10.1002/jper.23-0796 · Cited by 2
Current Understanding of the Role of Autophagy in the Treatment of Myeloid Leukemia
Kubota, Y., & Kimura, S. H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212219 · Cited by 3
The Lysosome, Elixir of Neural Stem Cell Youth
Simic, M., & Dillin, A. G. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.04.017 · Cited by 3
Autophagy on the road to longevity and aging
Manifava, M., & Ktistakis, N. T. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822003-0.00002-4 · Cited by 2
Autophagy in hematopoiesis and leukemogenesis
Ianniciello, A., & Helgason, G. V. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822003-0.00021-8 · Cited by 2
Liu, Z., Yan, N. J., Chen, Y., & Hu, B. (2022) · Cells Tissues Organs · doi:10.1159/000527212 · Cited by 2
Li, K., Shi, L., Yu, A., Meng, W.-H., & Xie, K.-P. (2023) · Synlett · doi:10.1055/a-2201-3612 · Cited by 2
Transglutaminase Type 2 is Involved in the Hematopoietic Stem Cells Homeostasis
Oliverio, S., Beltran, J. S. O., Occhigrossi, L., Bordoni, V., Agrati, C., D’Eletto, M., Rossin, F., Borelli, P., Amarante-Mendes, G. P., Demidov, O. N., et al. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920100041 · Cited by 2
Blomfield, I. M., Rocamonde, B., Masdeu, M. D. M., Mulugeta, E., Vaga, S., van den Berg, D. L. C., Huillard, E., Urbán, N., & Guillemot, F. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3219271 · Cited by 2
Autophagy slows the aging of Germline stem cells in Drosophila through modulation of E-cadherinPreprint
Murmu, N., & Shravage, B. V. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.31.486570 · Cited by 2
Bnip3lb-driven mitophagy sustains expansion of the embryonic hematopoietic stem cell poolPreprint
Meader, E., Walcheck, M. T., Leder, M. R., Jing, R., Wrighton, P. J., Sugden, W. W., Najia, M. A. T., Oderberg, I. M., Taylor, V. M., LeBlanc, Z. C., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.23.614531 · Cited by 2
Stathmin 1 regulates mitophagy and cellular function in hematopoietic stem cellsPreprint
Paracatu, L. C., Schuetz, M., Dong, Q., Warmka, M. G., Valin, L., Jones, A., Hunt, P., Petermeier, C., Wang, J., Roundy, N., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.10.642434 · Cited by 2
Ageing and its role in modulating healthy and tumour-associated macrophages
Duong, L., Jackaman, C., & Nelson, D. J. (2024) · Ageing and Cancer Research & Treatment · doi:10.37155/2972-4759-2024-02-01-1 · Cited by 1
Kumar, S., Vassallo, J. D., Nattamai, K., Hassan, A., Vollmer, A., Karns, R. A., Saçma, M., Nemkov, T. G., D’Alessandro, A., & Geiger, H. (2024) · Aging Cell · doi:10.1111/acel.14324 · Cited by 1
Jahan, S., Maganti, H. B., Patel, J., Pasha, R. P. K., Doxtator, E., Manesia, J. K., & Pineault, N. (2025) · Vox Sanguinis · doi:10.1111/vox.70012 · Cited by 1
Li, Y., Cheng, P., Zhang, H., Chen, S., Liu, H., Wang, K., Wang, J., & Kang, X. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47121001 · Cited by 1
Hsp70-Bim interaction mediated mitophagy as a potential therapeutic target for CML stem cells
Song, T., Song, Y., Zhang, H., Hu, Z., Yin, F., Jiang, M., Zhang, Y., Wang, Z., & Zhang, Z. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102751 · Cited by 1
From Hero to Hijacker: Autophagy’s Double Life in Immune Patrols and Cancer Escape
Garampon, F., & Claude‐Taupin, A. (2026) · Cells · doi:10.3390/cells15020102 · Cited by 1
Autophagy in emerging and highly concerned severe zoonotic infectious diseases
Qi, Y., Wang, L., Wu, S., Meng, C., Chu, Y., Yin, Y., & Jiao, H. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1761571 · Cited by 1
Lack of MDA5 delays hematopoietic aging by modulating inflammaging and proteostasis in mice
Bergo, V., Bousounis, P., Vu, G. T., Douté, M., Polyzou, A., Lalioti, M., Grigorash, B. B., Tsurkan, L., Morchel, N., Deboutte, W., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69424-x · Cited by 3
Non-necroptotic MLKL function damages mitochondria and promotes hematopoietic stem cell aging
Yamada, Y., Yang, J., Tsuchiya, A., Watanabe, Y., Koide, S., Murai, S., Sorimachi, Y., Fukuda, Y., Sumiyama, K., Sagara, H., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-71060-4 · Cited by 5
Aging mechanisms and rejuvenation strategies for hematopoietic stem cells
Zhang, Y., Xu, Y., Shi, W., Cao, D., Guo, D.-A., & Yue, R. (2026) · Genome biology · doi:10.1186/s13059-026-04119-6 · Cited by 1
Tian, X., Wu, B., Yang, K., Wang, Y., Li, Y., Guan, J., Wang, K., Zhao, Y., Sun, K., Ling, Y., et al. (2026) · Cell stem cell · doi:10.1016/j.stem.2026.05.012 · Cited by 2
Vitamin C attenuates primate bone marrow aging at the molecular and progenitor level
Ye, Y., Zhang, H., Xin, Z., Sun, W., Liu, L., Xiong, M., Zhao, H., Zhang, Y., Geng, J., Zhao, L., et al. (2026) · Cell stem cell · doi:10.1016/j.stem.2026.06.006 · Cited by 1
Wang, W., Xiao, L., Cui, C., Yin, G., Ren, W., & Wang, X. (2023) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2023.101583 · Cited by 1
Multi-lineage Differentiation from Hematopoietic Stem Cells
Wang, X., Liu, S., & Yu, J. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-981-99-7471-9_10 · Cited by 1
Abnormal expression of CUX1 influences autophagy activation in paroxysmal nocturnal hemoglobinuria
Wu, J., Li, L., Liu, Z., Wang, H., Chen, Y., Zeng, L., Wang, G., Liu, H., & Fu, R. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae008 · Cited by 1
Autophagy accompanying the developmental process of male germline stem cells
Jiang, Z., Chen, L., Wang, T., Zhao, J., Liu, S., He, Y., Wang, L., & Wu, H. (2024) · Cell and Tissue Research · doi:10.1007/s00441-024-03910-w · Cited by 1
Fang, X., Yao, X., Zhang, Y., Tian, Z., Wang, M., Li, P., & Cai, X. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153770 · Cited by 1
Balomenos, P., Dragomir, A., Tsakalidis, A. K., & Bezerianos, A. (2020) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc44109.2020.9176556 · Cited by 1
He, Y., & Zhou, D. (2020) · Blood Science · doi:10.1097/bs9.0000000000000060 · Cited by 1
Novel strategies to overcome drug resistance in liver cancer
Wang, Y. (2018) · Figshare · Cited by 1
Genetic Landscape of Electron Transport Chain Complex I Dependency in Acute Myeloid LeukemiaPreprint
Baccelli, I., Gareau, Y., Lehnertz, B., Gingras, S., Spinella, J.-F., Beautrait, A., Corneau, S., Mayotte, N., Boivin, I., Girard, S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/513887 · Cited by 1
Stem cell quiescence requires PRC2/PRC1-mediated mitochondrial checkpointPreprint
Ishibashi, J. R., Taslim, T. H., Hussein, A., Brewer, D., Liu, S., Harper, S., Nguyen, B. N., Dang, J., Chen, A., del Castillo, D., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.21.440825 · Cited by 1
Stressed and disoriented: stromal autophagy regulates HSCs
Hurwitz, S. N., & Kurre, P. (2022) · Blood · doi:10.1182/blood.2021014337 · Cited by 1
Puri, D., Kelkar, A., Bhaskar, G. S., & Subramanyam, D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.29.486206 · Cited by 1
Perdiguero, E., García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00138-3 · Cited by 1
Johnson, C. S., Sham, K., Belluschi, S., Wang, X., Lau, W. W. Y., Kaufmann, K. B., Krivdova, G., Calderbank, E. F., Mende, N., McLeod, J. L., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.17.516906 · Cited by 1
Watanuki, S., Kobayashi, H., Sugiura, Y., Yamamoto, M., Karigane, D., Shiroshita, K., Sorimachi, Y., Fujita, S., Morikawa, T., Koide, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.16.532898 · Cited by 1
Gcn5 and mTORC1 mediated regulation of autophagy controls Drosophila blood cell homeostasisPreprint
Arjun, A., Kunjumon, M., Math, S., Kata, L., & Khadilkar, R. J. (2024) · eLife · doi:10.7554/elife.91615 · Cited by 1
Arjun, A., Math, S., Kata, L., & Khadilkar, R. J. (2024) · eLife · doi:10.7554/elife.91615.1 · Cited by 1
Yu, C.-H., Malijauskaite, S., Hinze, C., Franzoni, M., Hickey, S., Marcar, L., Peak‐Chew, S., Cryar, A., Bain, C., Marsden, J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.01.606017 · Cited by 1
Varesi, A., Nagree, M. S., Biasio, I. D., Zeng, A. G. X., Shah, S., Kim, H., Zhang, M., Murison, A., Dick, J. E., & Xie, S. Z.-J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.11.659017 · Cited by 1
Proteostasis Stress Drives Stem Cell Aging, Clonal Hematopoiesis and LeukemiaPreprint
Zhou, F., Le, M. K., Wang, H. C., Yang, W., Wang, H., Tiwari, A., Cen, X., Sunshine, M. J., Magee, J. A., & Signer, R. A. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.27.690982 · Cited by 1
Self-consumption will keep your blood young
Strzyz, P. J. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.19
Papers of note in Nature 543 (7644)
VanHook, A. M. (2017) · Science Signaling · doi:10.1126/scisignal.aan1406
Kulkarni, R. S., Bajaj, M. S., & Kale, V. P. (2018) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-98146-8_3
Temporal inhibition of autophagy reveals segmental reversal of aging with increased cancer riskPreprint
Cassidy, L. D., Young, A. R. J., Young, C., Soilleux, E. J., Fielder, E., Weigand, B. M., Brais, R. J., Wiggins, K. A., Clarke, M. C. H., Jurk, D., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/528984
Relevance of Autophagy in Cancer Stem Cell and Therapeutic
Sinha, N. (2020) · Springer eBooks · doi:10.1007/978-981-15-6930-2_10
Li, Z., Liu, X., Liu, X., Du, Y., Zhu, Y., Lv, L., Zhang, X., Liu, Y., Zhang, P., & Zhou, Y. (2020) · Research Square · doi:10.21203/rs.3.rs-115769/v1
Ames, K. T., Kaur, I., Shi, Y., Tong, M., Sinclair, T., Hemmati, S., Glushakow-Smith, S. G., Tein, E., Gurska, L. M., Dubin, R., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.04.412593
Tan, Y., Xu, X., Dai, J., Yin, Y., He, X., Zhang, Y., Zhu, T.-X., An, Y., Tian, B., & Chen, F. (2020) · Research Square · doi:10.21203/rs.3.rs-122498/v1
Hair Regeneration by Small Molecules That Activate AutophagyPreprint
Chai, M., Jiang, M., Vergnes, L., Fu, X., de Barros, S. C., Jiao, J., Herschman, H. R., Crooks, G. M., Reue, K., & Huang, J. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3188356
Wang, W., Xiao, L., Cui, C., Liu, D., Yin, G., Guo, Z., & Wang, X. (2021) · Research Square · doi:10.21203/rs.3.rs-227201/v1
Dysregulated myogenesis and autophagy in genetically induced pulmonary emphysemaPreprint
Balnis, J., Drake, L. A., Singer, D. V., Vincent, C. E., Korponay, T. C., D'Armiento, J. M., Lee, C. G., Elias, J. A., Singer, H. A., & Jaitovich, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.08.450201
Metabolic reprogramming and redox perturbations
Aboushousha, R. (2021) · Research Publications (Maastricht University) · doi:10.26481/dis.20211208ra
Secretory MPP3 Reinforce Myeloid Differentiation Trajectory and Amplify Myeloid Cell ProductionPreprint
Kang, Y.-A., Paik, H., Zhang, S. Y., Chen, J., Warr, M. R., Fan, R., & Passegue, E. A. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3971148
Self-citationPrincipales medidas fiscales en la Ley 13/1997, de 23 de diciembre, de la Generalitat Valenciana
Clari, M. L. C. (2008) · Dialnet (Universidad de la Rioja)
Lazarovici, P. (2021) · Springer eBooks · doi:10.1007/978-3-030-22009-9_432
An Insight of Autophagy and Cellular Senescence: One Promising Approach for Senescence Delaying
(2022) · Journal of Contemporary Medical Practice · doi:10.53469/jcmp.2022.04(03).11
Yang, R., Shi, Y., Wang, S., Zhang, W., Zhu, Y., Fan, Z., Huang, Y., & Li, F. (2022) · Research Square · doi:10.21203/rs.3.rs-1443993/v1
Chu, Y., Yue, C., Peng, W., Chen, W., Zhang, Y., He, G., Liu, C., Zhang, N., Li, J., Liu, L., et al. (2020) · Research Square · doi:10.21203/rs.3.rs-43803/v1
Méndez‐Ferrer, S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732563533.793575319
Chu, Y., Yue, C., Peng, W., Chen, W., Zhang, Y., He, G., Liu, C., Zhang, N., Li, J., Liu, L., et al. (2020) · doi:10.21203/rs.3.rs-25663/v1
Krause, D. S. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733947391.793583300
Faculty Opinions recommendation of Understanding intrinsic hematopoietic stem cell aging.
Méndez‐Ferrer, S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737043526.793575345
Lazarovici, P. (2019) · Springer eBooks · doi:10.1007/978-3-319-69892-2_432-1
Jiang, X., & Rothe, K. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733947391.793554355
Mitochondrial and Lysosomal Metabolism in Hematopoietic Stem Cells
Mochizuki‐Kashio, M., Ito, K., & Nakamura‐Ishizu, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00077-8
Glycolytic metabolism and differentiation remodeling of hematopoietic stem cells in lung cancerPreprint
Guo, Z., Pu, S., Yang, L., Liu, Y., Li, X., Zhao, H., Zhou, Z., & Yang, C. (2022) · Research Square · doi:10.21203/rs.3.rs-2201060/v1
The Role of Autophagy in the Regulation of Hematopoietic Stem Cells
Budgude, P., Teli, P., Vaidya, A., & Kale, V. P. (2022) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-031-17362-2_5
Ding, Q., Zhou, J., Yu, L., Wang, Q., Yao, C., Jiang, R., Meng, Q., Wang, H., Chen, Y., & Guo, B. (2022) · Stem Cell Reviews and Reports · doi:10.1007/s12015-022-10480-3
Ainciburu, M. (2022) · Deposito Adademico Digital Universidad De Navarra (University of Navarra) · doi:10.15581/10171/65224
Induction of mitophagy reverts age-associated decline of the hematopoietic and immune systemsPreprint
Girotra, M., Chiang, Y.-H., Charmoy, M., Ginefra, P., Schyrr, F., Franco, F., Ho, P., Naveiras, O., Auwerx, J. H., Held, W., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.30.534925
Yin, Z., Huang, G., Gu, C., Liu, Y., Yang, J., & Fei, J. (2023) · doi:10.1158/1078-0432.c.6529803
Aoyagi, Y., Hayashi, Y., Harada, Y., Choi, K., Matsunuma, N., Sadato, D., Maemoto, Y., Ito, A., Yanagi, S., Starczynowski, D. T., et al. (2023) · doi:10.1158/2159-8290.c.6549430.v1
Loss of PINK1 promotes the expansion of hematopoietic cells via upregulating autophagyPreprint
Yi, Z., Chen, X., & Chun‐Hang, A. (2023) · Research Square · doi:10.21203/rs.3.rs-2671385/v1
Watanuki, S., Kobayashi, H., Sugiura, Y., Yamamoto, M., Karigane, D., Shiroshita, K., Sorimachi, Y., Koide, S., Oshima, M., Nishiyama, A., et al. (2023) · eLife · doi:10.7554/elife.87674.1
Gilchrist, J. J., Fang, H., Danielli, S., Tomková, M., Nassiri, I., Ng, E., Tong, O., Taylor, C. A., Al‐Mossawi, H., Lau, E., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.17.541041
Gcn5 and mTORC1 mediated regulation of autophagy controls Drosophila blood cell homeostasis
Reeja, A. A., Kunjumon, M., Math, S., Kata, L., & Khadilkar, R. J. (2026) · eLife · doi:10.1101/2023.07.04.547637
Skinder, N., Fernández, I. S., Dethmers-Ausema, A., Weersing, E., & de Haan, G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.14.553203
Autophagy regulates the maturation of hematopoietic precursors in the embryoPreprint
Liu, Y., Shi, L., Chen, Y., Luo, S., Chen, Y., Chen, H., Lan, W., Lu, X., Cao, Z., Ye, Z., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3288232/v1
Fueling fate: Metabolic crosstalk in the bone marrow microenvironment
Lisi-Vega, L. E., & Méndez‐Ferrer, S. (2023) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2023.08.001
Basic Hematopoiesis and Leukemia Stem Cells
Hwang, W. Y. K., Bari, S., Ng, L. G., Itahana, K., Li, S., Koh, J. Y. P., & Than, H. (2023) · Springer eBooks · doi:10.1007/978-981-99-3810-0_1
Vitamin B3 Rescues Mandibular Osteoporosis in Bmi-1–Deficient Mice by Regulating AutophagyPreprint
Liu, S., Chu, Y., Yan, L., Chen, H., Ge, J., Cai, S., Wu, J., & Gong, A. (2023) · Research Square · doi:10.21203/rs.3.rs-3691125/v1
Ferritinophagy is a Druggable Vulnerability of Quiescent Leukemic Stem CellsPreprint
Larrue, C., Mouche, S., Angelino, P., Sajot, M., Birsen, R., Vergez, F., Récher, C., Mas, V. M., Gu, Q., Xu, J., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.18.572101
The potential use of recombinant immunotoxin and BCL-2 inhibitors for leukemic stem cell elimination
Rizkiawan, D. E. (2023) · World Journal of Advanced Research and Reviews · doi:10.30574/wjarr.2023.20.3.2571
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.87674.2
Epidermal Growth Factor Rejuvenates Aged Hematopoietic Stem CellsPreprint
Chang, V. Y., He, Y., Grohe, S., Brady, M. J., Chan, A., Kadam, R., Fang, T., Pang, A., Pohl, K. A., Tran, E., et al. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4685388
Immune System Influence on Hematopoietic Stem Cells and Leukemia Development
Perry, J. M. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-981-99-7471-9_8
Time-series analysis of hematopoietic stem cells
Han, J., Duan, S., Li, Y., & Xin, C. (2024) · Medicine · doi:10.1097/md.0000000000036509
Metadata
- Authors
- Ho, T. T., Warr, M. R., Adelman, E. R., Lansinger, O. M., Flach, J., Verovskaya, E. V., Figueroa, M. E., & Passegué, E.
- Affiliations
- University of California, San Francisco (US)
- University of Michigan (US)
- ORCID
- Venue
- Nature
- Published
- 2017-03
- Volume
- 543
- Issue
- 7644
- Pages
- 205-210
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5344718
- OpenAlex
- W2592615787
- Cited by
- 896
- References
- 42
- Citations by year
- 2026: 58 · 2025: 67 · 2024: 95 · 2023: 103 · 2022: 107 · 2021: 124 · 2020: 118 · 2019: 93 · 2018: 90 · 2017: 40
- FWCI
- 71.87
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute on Aging (T32AG000114)
- National Heart, Lung, and Blood Institute (R01HL126947)
- National Cancer Institute (R01CA184014)
- National Institute of General Medical Sciences (T32GM008284)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK063720)
- Topics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- autophagy, hematopoietic stem cells, cellular aging, stem cell self-renewal, mitochondrial accumulation, myeloid differentiation, epigenetic regulation, metabolic stress, regenerative capacity, stem cell quiescence
- MeSH terms
- Cell Self Renewal, Animals, Autophagy, Female, Hematopoiesis, Hematopoietic Stem Cells, Male, Mitochondria, Cellular Senescence, Myeloid Cells, Epigenesis, Genetic, Mice
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