Grego-Bessa Joaquim, Bloomekatz Joshua, Castel Pau, Omelchenko Tatiana, Baselga José, Anderson Kathryn V
Developmental Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, United States.
Human Oncology and Pathogenesis Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, United States.
Elife. 2016 Jan 26;5:e12034. doi: 10.7554/eLife.12034.
Epithelial morphogenesis and stability are essential for normal development and organ homeostasis. The mouse neural plate is a cuboidal epithelium that remodels into a columnar pseudostratified epithelium over the course of 24 hr. Here we show that the transition to a columnar epithelium fails in mutant embryos that lack the tumor suppressor PTEN, although proliferation, patterning and apical-basal polarity markers are normal in the mutants. The Pten phenotype is mimicked by constitutive activation of PI3 kinase and is rescued by the removal of PDK1 (PDPK1), but does not depend on the downstream kinases AKT and mTORC1. High resolution imaging shows that PTEN is required for stabilization of planar cell packing in the neural plate and for the formation of stable apical-basal microtubule arrays. The data suggest that appropriate levels of membrane-associated PDPK1 are required for stabilization of apical junctions, which promotes cell elongation, during epithelial morphogenesis.
上皮形态发生和稳定性对于正常发育和器官稳态至关重要。小鼠神经板是一种立方形上皮,在24小时的过程中重塑为柱状假复层上皮。在这里我们表明,在缺乏肿瘤抑制因子PTEN的突变胚胎中,向柱状上皮的转变失败,尽管突变体中的增殖、模式形成和顶-基极性标记是正常的。PI3激酶的组成型激活模拟了Pten表型,而去除PDK1(PDPK1)可挽救该表型,但不依赖于下游激酶AKT和mTORC1。高分辨率成像显示,PTEN是神经板中平面细胞堆积稳定以及稳定的顶-基微管阵列形成所必需的。数据表明,在上皮形态发生过程中,稳定顶端连接需要适当水平的膜相关PDPK1,这促进细胞伸长。