Van Keymeulen Alexandra, Fioramonti Marco, Centonze Alessia, Bouvencourt Gaëlle, Achouri Younes, Blanpain Cédric
Laboratory of Stem Cells and Cancer, Université Libre de Bruxelles (ULB), Brussels 1070, Belgium.
Laboratory of Stem Cells and Cancer, Université Libre de Bruxelles (ULB), Brussels 1070, Belgium.
Cell Rep. 2017 Aug 15;20(7):1525-1532. doi: 10.1016/j.celrep.2017.07.066.
The mammary gland (MG) is composed of different cell lineages, including the basal and the luminal cells (LCs) that are maintained by distinct stem cell (SC) populations. LCs can be subdivided into estrogen receptor (ER) and ER cells. LCs act as the cancer cell of origin in different types of mammary tumors. It remains unclear whether the heterogeneity found in luminal-derived mammary tumors arises from a pre-existing heterogeneity within LCs. To investigate LC heterogeneity, we used lineage tracing to assess whether the ER lineage is maintained by multipotent SCs or by lineage-restricted SCs. To this end, we generated doxycycline-inducible ER-rtTA mice that allowed us to perform genetic lineage tracing of ER LCs and study their fate and long-term maintenance. Our results show that ER cells are maintained by lineage-restricted SCs that exclusively contribute to the expansion of the ER lineage during puberty and their maintenance during adult life.
乳腺(MG)由不同的细胞谱系组成,包括基底细胞和管腔细胞(LCs),它们由不同的干细胞(SCs)群体维持。LCs可细分为雌激素受体(ER)阳性和ER阴性细胞。LCs在不同类型的乳腺肿瘤中作为肿瘤起源细胞。尚不清楚在管腔源性乳腺肿瘤中发现的异质性是否源于LCs内预先存在的异质性。为了研究LC异质性,我们使用谱系追踪来评估ER谱系是由多能SCs还是由谱系限制SCs维持。为此,我们生成了强力霉素诱导的ER-rtTA小鼠,这使我们能够对ER LCs进行遗传谱系追踪,并研究它们的命运和长期维持。我们的结果表明,ER阳性细胞由谱系限制SCs维持,这些SCs在青春期专门促进ER谱系的扩张,并在成年期维持其存在。