Blaas Leander, Pucci Fabio, Messal Hendrik A, Andersson Agneta B, Josue Ruiz E, Gerling Marco, Douagi Iyadh, Spencer-Dene Bradley, Musch Alexandra, Mitter Richard, Bhaw Leena, Stone Richard, Bornhorst Dorothee, Sesay Abdul K, Jonkers Jos, Stamp Gordon, Malanchi Ilaria, Toftgård Rune, Behrens Axel
Center for Innovative Medicine (CIMED), Department of Biosciences and Nutrition, Karolinska Institutet, Novum, 141 83 Huddinge, Sweden.
Adult Stem Cell Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Nat Cell Biol. 2016 Dec;18(12):1346-1356. doi: 10.1038/ncb3434. Epub 2016 Oct 31.
The mammary gland is composed of a complex cellular hierarchy with unusual postnatal plasticity. The identities of stem/progenitor cell populations, as well as tumour-initiating cells that give rise to breast cancer, are incompletely understood. Here we show that Lgr6 marks rare populations of cells in both basal and luminal mammary gland compartments in mice. Lineage tracing analysis showed that Lgr6 cells are unipotent progenitors, which expand clonally during puberty but diminish in adulthood. In pregnancy or following stimulation with ovarian hormones, adult Lgr6 cells regained proliferative potency and their progeny formed alveoli over repeated pregnancies. Oncogenic mutations in Lgr6 cells resulted in expansion of luminal cells, culminating in mammary gland tumours. Conversely, depletion of Lgr6 cells in the MMTV-PyMT model of mammary tumorigenesis significantly impaired tumour growth. Thus, Lgr6 marks mammary gland progenitor cells that can initiate tumours, and cells of luminal breast tumours required for efficient tumour maintenance.
乳腺由具有异常出生后可塑性的复杂细胞层级结构组成。对于干细胞/祖细胞群体以及引发乳腺癌的肿瘤起始细胞的身份,我们尚未完全了解。在此,我们表明Lgr6标记小鼠乳腺基底和管腔隔室中的稀有细胞群体。谱系追踪分析表明,Lgr6细胞是单能祖细胞,在青春期期间克隆性扩增,但在成年期减少。在怀孕或用卵巢激素刺激后,成年Lgr6细胞恢复增殖能力,并且它们的后代在多次怀孕过程中形成腺泡。Lgr6细胞中的致癌突变导致管腔细胞扩张,最终形成乳腺肿瘤。相反,在MMTV-PyMT乳腺肿瘤发生模型中耗尽Lgr6细胞会显著损害肿瘤生长。因此,Lgr6标记了能够引发肿瘤的乳腺祖细胞以及高效维持肿瘤所需的乳腺管腔肿瘤细胞。