Cited by 817Hematopoietic Stem Cell TransplantationPI3K/AKT/mTOR signaling in cancerAcute Myeloid Leukemia Research

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PTEN maintains haematopoietic stem cells and acts in lineage choice and leukaemia prevention

Zhang, Jiwang, Grindley, Justin C., Yin, Tong, Jayasinghe, Sachintha, He, Xi C., Ross, Jason T., Haug, Jeffrey S., Rupp, Dawn, Porter-Westpfahl, Kimberly S., Wiedemann, Leanne M., Wu, Hong, Li, Linheng·2006·Nature

DOI 10.1038/nature04747

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Abstract

Haematopoietic stem cells (HSCs) must achieve a balance between quiescence and activation that fulfils immediate demands for haematopoiesis without compromising long-term stem cell maintenance, yet little is known about the molecular events governing this balance. Phosphatase and tensin homologue (PTEN) functions as a negative regulator of the phosphatidylinositol-3-OH kinase (PI(3)K)-Akt pathway, which has crucial roles in cell proliferation, survival, differentiation and migration. Here we show that inactivation of PTEN in bone marrow HSCs causes their short-term expansion, but long-term decline, primarily owing to an enhanced level of HSC activation. PTEN-deficient HSCs engraft normally in recipient mice, but have an impaired ability to sustain haematopoietic reconstitution, reflecting the dysregulation of their cell cycle and decreased retention in the bone marrow niche. Mice with PTEN-mutant bone marrow also have an increased representation of myeloid and T-lymphoid lineages and develop myeloproliferative disorder (MPD). Notably, the cell populations that expand in PTEN mutants match those that become dominant in the acute myeloid/lymphoid leukaemia that develops in the later stages of MPD. Thus, PTEN has essential roles in restricting the activation of HSCs, in lineage fate determination, and in the prevention of leukaemogenesis.

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SLAM Family Receptors Distinguish Hematopoietic Stem and Progenitor Cells and Reveal Endothelial Niches for Stem Cells
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
Identification of the haematopoietic stem cell niche and control of the niche size
Zhang, J., Niu, C. S., Ye, L., Huang, H., He, X. C., Tong, W.-G., Ross, J., Haug, J., Johnson, T. J., Feng, J. Q., et al. (2003) · Nature · doi:10.1038/nature02041 · Cited by 2,948
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Akashi, K., Traver, D., Miyamoto, T., & Weissman, I. L. (2000) · Nature · doi:10.1038/35004599 · Cited by 2,617
Identification of Clonogenic Common Lymphoid Progenitors in Mouse Bone Marrow
Kondo, M., Weissman, I. L., & Akashi, K. (1997) · Cell · doi:10.1016/s0092-8674(00)80453-5 · Cited by 2,253
Tie2/Angiopoietin-1 Signaling Regulates Hematopoietic Stem Cell Quiescence in the Bone Marrow Niche
Arai, F., Hirao, A., Ohmura, M., Sato, H., Matsuoka, S., Takubo, K., Ito, K., Koh, G. Y., & Suda, T. (2004) · Cell · doi:10.1016/j.cell.2004.07.004 · Cited by 1,958
Recruitment of Stem and Progenitor Cells from the Bone Marrow Niche Requires MMP-9 Mediated Release of Kit-Ligand
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Inducible Gene Targeting in Mice
Kühn, R., Schwenk, F., Aguet, M., & Rajewsky, K. (1995) · Science · doi:10.1126/science.7660125 · Cited by 1,641
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Cheng, T., Rodrigues, N., Shen, H., Yang, Y.-G., Dombkowski, D., Sykes, M., & Scadden, D. T. (2000) · Science · doi:10.1126/science.287.5459.1804 · Cited by 1,339
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Chen, C., Liu, Y., Liu, Y., & Zheng, P. (2010) · Journal of Clinical Investigation · doi:10.1172/jci43873 · Cited by 105
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Fukuyama, M., Sakuma, K., Park, R., Hidefumi, K., Nagaya, R., Atsumi, Y., Shimomura, Y., Takahashi, S., Kajiho, H., Rougvie, A. E., et al. (2012) · Biology Open · doi:10.1242/bio.2012836 · Cited by 105
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Sabnis, A. J., Cheung, L. S., Dail, M., Kang, H. C., Santaguida, M. A., Hermiston, M. L., Passegue, E. A., Shannon, K., & Braun, B. S. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000059 · Cited by 102
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Gan, B., & DePinho, R. A. (2009) · Cell Cycle · doi:10.4161/cc.8.7.8045 · Cited by 99
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Ciuffreda, L., Falcone, I., Incani, U. C., Curatolo, A. D., Conciatori, F., Matteoni, S., Vari, S., Vaccaro, V., Cognetti, F., & Milella, M. (2014) · Advances in Biological Regulation · doi:10.1016/j.jbior.2014.07.002 · Cited by 85
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Xiao, W., Hong, H., Kawakami, Y., Lowell, C. A., & Kawakami, T. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34013 · Cited by 82
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Sordillo, P. P., & Helson, L. (2015) · PubMed · Cited by 77
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Qian, Z., Chen, L., Fernald, A. A., Williams, B. O., & Beau, M. M. L. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20080578 · Cited by 81
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Yang, Q., Kardava, L., Leger, A. J. S., Martincic, K., Varnum‐Finney, B., Bernstein, I. D., Milcarek, C., & Borghesi, L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.9.5885 · Cited by 72
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Qiao, W., Wang, W., Laurenti, E., Turinsky, A. L., Wodak, S. J., Bader, G. D., Dick, J. E., & Zandstra, P. W. (2014) · Molecular Systems Biology · doi:10.15252/msb.20145141 · Cited by 72
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Guo, W., Schubbert, S., Chen, J. Y., Valamehr, B. B., Mosessian, S., Shi, H., Dang, N. H., Garcia, C., Theodoro, M. F., Varella‐Garcia, M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006937108 · Cited by 73
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Hoshii, T., Kasada, A., Hatakeyama, T., Ohtani, M., Tadokoro, Y., Naka, K., Ikenoue, T., Ikawa, T., Kawamoto, H., Fehling, H. J., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320265111 · Cited by 63
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Authors: Zhang, J., Grindley, J. C., Yin, T., Jayasinghe, S., He, X. C., Ross, J. T., Haug, J. S., Rupp, D., Porter-Westpfahl, K. S., Wiedemann, L. M., Wu, H., & Li, L.
Affiliations: Stowers Institute for Medical Research (US)
University of California, Los Angeles (US)
Corresponding author: Li, Linheng
ORCID: Zhang, Jiwang
Yin, Tong
Jayasinghe, Sachintha
He, Xi C.
Haug, Jeffrey S.
Wiedemann, Leanne M.
Wu, Hong
Li, Linheng
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2006-04-23
Volume: 441
Issue: 7092
Pages: 518-522
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature04747
OpenAlex: W2057403210
Cited by: 817
References: 30
Citations by year: 2026: 7 · 2025: 6 · 2024: 9 · 2023: 19 · 2022: 18 · 2021: 30 · 2020: 22 · 2019: 29 · 2018: 24 · 2017: 29 · 2016: 48 · 2015: 40 · 2014: 58 · 2013: 61 · 2012: 55
FWCI: 43.78
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
RePEc: Research Papers in Economics (submittedVersion)
Topics: Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
Keywords: PTEN, hematopoietic stem cells, leukemia stem cells, PI3K/Akt signaling, stem cell self-renewal, HSC quiescence, lineage choice, myeloproliferative neoplasms, acute myeloid leukemia, acute lymphoblastic leukemia, rapamycin, bone marrow microenvironment, haematopoietic reconstitution
MeSH terms: Animals, Cell Count, Cell Cycle, Hematopoietic Stem Cells, Leukemia, Mutation, Gene Expression, Cell Lineage, Cyclin D1, Cell Proliferation, PTEN Phosphohydrolase, Mice

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PTEN maintains haematopoietic stem cells and acts in lineage choice and leukaemia prevention

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