Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, MA 02114, USA; Department of Pediatrics, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Internal Medicine, Pulmonary and Critical Care Unit, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA.
Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, MA 02114, USA.
Dev Cell. 2014 Jul 28;30(2):151-65. doi: 10.1016/j.devcel.2014.06.004. Epub 2014 Jul 17.
Our understanding of how stem cells are regulated to maintain appropriate tissue size and architecture is incomplete. We show that Yap (Yes-associated protein 1) is required for the actual maintenance of an adult mammalian stem cell. Without Yap, adult airway basal stem cells are lost through their unrestrained differentiation, resulting in the simplification of a pseudostratified epithelium into a columnar one. Conversely, Yap overexpression increases stem cell self-renewal and blocks terminal differentiation, resulting in epithelial hyperplasia and stratification. Yap overexpression in differentiated secretory cells causes them to partially reprogram and adopt a stem cell-like identity. In contrast, Yap knockdown prevents the dedifferentiation of secretory cells into stem cells. We then show that Yap functionally interacts with p63, the cardinal transcription factor associated with myriad epithelial basal stem cells. In aggregate, we show that Yap regulates all of the cardinal behaviors of airway epithelial stem cells and determines epithelial architecture.
我们对于干细胞如何受到调控以维持适当的组织大小和结构的理解还不完整。我们发现 Yap(Yes 相关蛋白 1)对于维持成年哺乳动物干细胞的实际状态是必需的。没有 Yap,成年气道基底干细胞会通过不受控制的分化而丧失,导致假复层上皮简化为柱状上皮。相反, Yap 的过表达会增加干细胞的自我更新并阻止终端分化,从而导致上皮过度增生和分层。 Yap 在分化的分泌细胞中的过表达会导致它们部分重新编程并获得干细胞样特征。相比之下, Yap 的敲低会阻止分泌细胞向干细胞的去分化。然后,我们发现 yap 与 p63 (与众多上皮基底干细胞相关的主要转录因子)在功能上相互作用。总的来说,我们表明 yap 调节了气道上皮干细胞的所有主要行为,并决定了上皮结构。