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Distinct stem cells contribute to mammary gland development and maintenance
Abstract
The mammary epithelium is composed of several cell lineages including luminal, alveolar and myoepithelial cells. Transplantation studies have suggested that the mammary epithelium is maintained by the presence of multipotent mammary stem cells. To define the cellular hierarchy of the mammary gland during physiological conditions, we performed genetic lineage-tracing experiments and clonal analysis of the mouse mammary gland during development, adulthood and pregnancy. We found that in postnatal unperturbed mammary gland, both luminal and myoepithelial lineages contain long-lived unipotent stem cells that display extensive renewing capacities, as demonstrated by their ability to clonally expand during morphogenesis and adult life as well as undergo massive expansion during several cycles of pregnancy. The demonstration that the mammary gland contains different types of long-lived stem cells has profound implications for our understanding of mammary gland physiology and will be instrumental in unravelling the cells at the origin of breast cancers.
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“Lineage tracing experiments have also facilitated the identification of long-lived stem cells in the mammary epithelium36,37 and in glandular epithelia such as that found in the prostate38.”
From Molecular regulation of stem cell quiescence (2013) · cites this paper as [36]
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Cites
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907
Identification of stem cells in small intestine and colon by marker gene Lgr5
Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687
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
In vitro propagation and transcriptional profiling of human mammary stem/progenitor cellsPreprint
Dontu, G., Abdallah, W. M., Foley, J. M., Jackson, K. W., Clarke, M. F., Kawamura, M., & Wicha, M. S. (2003) · Genes & Development · doi:10.1101/gad.1061803 · Cited by 2,413
Generation of a functional mammary gland from a single stem cell
Shackleton, M., Vaillant, F., Simpson, K. J., Stingl, J., Smyth, G. K., Asselin-Labat, M.-L., Wu, L., Lindeman, G. J., & Visvader, J. E. (2006) · Nature · doi:10.1038/nature04372 · Cited by 2,005
Purification and unique properties of mammary epithelial stem cells
Stingl, J., Eirew, P. D., Ricketson, I., Shackleton, M. J., Vaillant, F., Choi, D., Li, H. I., & Eaves, C. J. (2006) · Nature · doi:10.1038/nature04496 · Cited by 1,581
Epidermal homeostasis: a balancing act of stem cells in the skin
Blanpain, C., & Fuchs, E. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2636 · Cited by 1,270
Self-citationKeeping abreast of the mammary epithelial hierarchy and breast tumorigenesisPreprint
Visvader, J. E. (2009) · Genes & Development · doi:10.1101/gad.1849509 · Cited by 603
An entire functional mammary gland may comprise the progeny from a single cell
Kordon, E. C., & Smith, G. H. (1998) · Development · doi:10.1242/dev.125.10.1921 · Cited by 553
Early restriction of peripheral and proximal cell lineages during formation of the lung
Perl, A. T., Wert, S. E., Nagy, A., Lobe, C. G., & Whitsett, J. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152238499 · Cited by 525
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Makarem, M., Spike, B. T., Dravis, C., Kannan, N., Wahl, G. M., & Eaves, C. J. (2013) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-013-9284-6 · Cited by 49
Single-cell RNA-Seq reveals cell heterogeneity and hierarchy within mouse mammary epithelia
Sun, H., Miao, Z., Zhang, X., Chan, U. I., Su, S. M., Guo, S., Wong, C. K. H., Xu, X., & Deng, C. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002297 · Cited by 45
Neutral lineage tracing of proliferative embryonic and adult mammary stem/progenitor cells
Lloyd‐Lewis, B., Davis, F. M., Harris, O. B., Hitchcock, J. R., & Watson, C. J. (2018) · Development · doi:10.1242/dev.164079 · Cited by 45
Notch and Wnt Dysregulation and Its Relevance for Breast Cancer and Tumor Initiation
Braune, E.-B., Seshire, A., & Lendahl, U. (2018) · Biomedicines · doi:10.3390/biomedicines6040101 · Cited by 45
Flemban, A. F., & Qualtrough, D. (2015) · Cancers · doi:10.3390/cancers7030866 · Cited by 44
Yallowitz, A. R., Alexandrova, E. M., Talos, F., Xu, S., Marchenko, N. D., & Moll, U. M. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2013.199 · Cited by 43
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Shum, W. W., Hill, E., Brown, D., & Breton, S. (2013) · Reproduction · doi:10.1530/rep-12-0510 · Cited by 44
Kwak, M., & Ghazizadeh, S. (2014) · Stem Cells and Development · doi:10.1089/scd.2014.0355 · Cited by 43
Jin, L., Qu, Y., Gomez, L. J., Chung, S., Han, B., Gao, B., Yue, Y., Gong, Y., Liu, X., Amersi, F. F., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.23817 · Cited by 45
Frank, S. B., Nelson, P. S., & Vasioukhin, V. I. (2018) · F1000Research · doi:10.12688/f1000research.14499.1 · Cited by 45
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Yuan, L., Xie, S., Bai, H., Liu, X., Cai, P., Lu, J., Wang, C., Lin, Z., Li, S., Guo, Y., et al. (2023) · Nature Methods · doi:10.1038/s41592-023-02039-y · Cited by 43
Many, A. M., & Brown, A. M. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101800 · Cited by 45
Wang, D., Gao, H., Bandyopadhyay, A. M., Wu, A., Yeh, I., Chen, Y., Zou, Y., Huang, C., Walter, C. A., Dong, Q., et al. (2014) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-13-0260 · Cited by 45
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Moumen, M., Chiche, A., Deugnier, M., Petit, V., Gandarillas, A., Glukhova, M. A., & Faraldo, M. M. (2012) · Stem Cells · doi:10.1002/stem.1090 · Cited by 44
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Li, L., Li, B., Li, M., Niu, C., Wang, G., Li, T., Król, E., Jin, W., & Speakman, J. R. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.07.015 · Cited by 44
Iglesia, M. D., Jayasinghe, R. G., Chen, S., Terekhanova, N. V., Herndon, J. M., Storrs, E. P., Karpova, A. Y., Zhou, D. C., Deen, N. N. A., Shinkle, A. T., et al. (2024) · Nature Cancer · doi:10.1038/s43018-024-00773-6 · Cited by 45
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Oliemuller, E., Kogata, N., Bland, P. J., Kriplani, D., Daley, F. M., Haider, S. A., Shah, V., Sawyer, E. J., & Howard, B. A. (2017) · The Journal of Pathology · doi:10.1002/path.4939 · Cited by 43
Goidts, V., Nakata, S., & Phillips, E. (2014) · Cancer Management and Research · doi:10.2147/cmar.s57846 · Cited by 41
Boras-Granic, K., Dann, P. R., & Wysolmerski, J. J. (2014) · Breast Cancer Research · doi:10.1186/s13058-014-0487-6 · Cited by 42
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Dumont-Lagacé, M., Brochu, S., St-Pierre, C., & Perreault, C. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302961 · Cited by 41
Remodeling of Murine Mammary Adipose Tissue during Pregnancy, Lactation, and Involution
Wang, Q. A., & Scherer, P. E. (2019) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-019-09434-2 · Cited by 38
Leung, Y., Kandyba, E. E., Chen, Y., Ruffins, S. W., & Kobielak, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074174 · Cited by 40
Dong, Q., Wang, D., Bandyopadhyay, A. M., Gao, H., Gorena, K. M., Hildreth, K., Rebel, V. I., Walter, C. A., Huang, C., & Sun, L. (2013) · Stem Cell Research · doi:10.1016/j.scr.2013.01.007 · Cited by 38
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Cocola, C., Molgora, S., Piscitelli, E., Veronesi, M. C., Greco, M., Bragato, C., Moro, M., Crosti, M., Gray, B. D., Milanesi, L., et al. (2016) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25737 · Cited by 39
Élias, S., Morgan, M. A., Bikoff, E. K., & Robertson, E. J. (2017) · Nature Communications · doi:10.1038/s41467-017-01971-w · Cited by 42
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Varès, G., Sai, S., Wang, B., Fujimori, A., Nenoi, M., & Nakajima, T. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.03.030 · Cited by 38
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Lee, H. J., & Ormandy, C. J. (2012) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2012.02.006 · Cited by 38
Han, Y., VILLARREAL-PONCE, A. P., Gutierrez, G., Nguyen, Q., Sun, P., Wu, T. H., Sui, B., Berx, G., Brabletz, T., Kessenbrock, K., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110240 · Cited by 37
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Sheridan, J. M., Ritchie, M. E., Best, S. A., Jiang, K., Beck, T. J., Vaillant, F., Liu, K., Dickins, R. A., Smyth, G. K., Lindeman, G. J., et al. (2015) · BMC Cancer · doi:10.1186/s12885-015-1187-z · Cited by 37
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Yallowitz, A. R., Li, D., Lobko, A., Mott, D., Nemajerová, A., & Marchenko, N. D. (2015) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-14-0360 · Cited by 36
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Rinaldi, L., & Benitah, S. A. (2014) · FEBS Journal · doi:10.1111/febs.12946 · Cited by 38
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Ferrari, N., Riggio, A. I., Mason, S. M., McDonald, L., King, A., Higgins, T., Rosewell, I. R., Neil, J. C., Smalley, M. J., Sansom, O. J., et al. (2015) · Scientific Reports · doi:10.1038/srep15658 · Cited by 35
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Xiang, H., Yuan, L., Gao, X., Alexander, P. B., Lopez, O. M., Lau, C. E., Ding, Y., Chong, M., Sun, T., Chen, R., et al. (2017) · Cell Discovery · doi:10.1038/celldisc.2017.19 · Cited by 33
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Stewart, T. A., Hughes, K., Stevenson, A. J., Marino, N., Ju, A. L., Morehead, M., & Davis, F. M. (2020) · Journal of Cell Science · doi:10.1242/jcs.248849 · Cited by 39
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Wu, A., Dong, Q., Gao, H., Shi, Y., Chen, Y., Zhang, F., Bandyopadhyay, A. M., Wang, D., Gorena, K. M., Huang, C., et al. (2016) · Scientific Reports · doi:10.1038/srep32190 · Cited by 31
Bresson, L., Faraldo, M. M., Di-Cicco, A., Quintanilla, M., Glukhova, M. A., & Deugnier, M. (2018) · Development · doi:10.1242/dev.160382 · Cited by 30
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Dong, Q., Gao, H., Shi, Y., Zhang, F., Gu, X., Wu, A., Wang, D., Chen, Y., Bandyopadhyay, A., Yeh, I.-T., et al. (2016) · Aging · doi:10.18632/aging.101082 · Cited by 29
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Zaragozá, R., García–Trevijano, E. R., Lluch, A. M., Ribas, G., & Vinã, J. R. (2015) · IUBMB Life · doi:10.1002/iub.1365 · Cited by 29
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Arendt, L. M., Keller, P. J., Skibinski, A., Goncalves, K., Naber, S. P., Buchsbaum, R. J., Gilmore, H. L., Come, S. E., & Kuperwasser, C. (2014) · Breast Cancer Research · doi:10.1186/s13058-014-0453-3 · Cited by 28
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Arendt, L. M., St. Laurent, J., Wronski, A., Caballero, S., Lyle, S. R., Naber, S. P., & Kuperwasser, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111442 · Cited by 27
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Metadata
- Authors
- Van Keymeulen, A., Rocha, A. S., Ousset, M., Beck, B., Bouvencourt, G., Rock, J., Sharma, N., Dekoninck, S., & Blanpain, C.
- Affiliations
- Université Libre de Bruxelles (BE)
- Duke Medical Center (US)
- Corresponding author
- Blanpain, Cédric
- Venue
- Nature
- Published
- 2011-10-09
- Volume
- 479
- Issue
- 7372
- Pages
- 189-193
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2082161467
- Cited by
- 854
- References
- 38
- Citations by year
- 2026: 24 · 2025: 38 · 2024: 41 · 2023: 44 · 2022: 30 · 2021: 55 · 2020: 62 · 2019: 51 · 2018: 73 · 2017: 55 · 2016: 54 · 2015: 91 · 2014: 83 · 2013: 81 · 2012: 68
- FWCI
- 36.95
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- mammary stem cells, mammary gland development, mammary epithelium, cellular hierarchy, lineage tracing, clonal expansion, multipotent stem cells, luminal cells, myoepithelial cells, alveolar cells, mammary gland morphogenesis, pregnancy, lactation
- MeSH terms
- Aging, Animals, Cell Differentiation, Epithelium, Female, Homeostasis, Lactation, Mammary Glands, Animal, Pregnancy, Stem Cells, Cell Transplantation, Cell Lineage, Multipotent Stem Cells, Mice
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