Chung SeYeon, Kim Sangjoon, Andrew Deborah J
Department of Cell Biology, The Johns Hopkins University School of Medicine, Baltimore, United States.
Elife. 2017 Mar 6;6:e22235. doi: 10.7554/eLife.22235.
Apical constriction is a widely utilized cell shape change linked to folding, bending and invagination of polarized epithelia. It remains unclear how apical constriction is regulated spatiotemporally during tissue invagination and how this cellular process contributes to tube formation in different developmental contexts. Using salivary gland (SG) invagination as a model, we show that regulation of expression by the Fork head transcription factor is required for apicomedial accumulation of Rho kinase and non-muscle myosin II, which coordinate apical constriction. We demonstrate that neither loss of spatially coordinated apical constriction nor its complete blockage prevent internalization and tube formation, although such manipulations affect the geometry of invagination. When apical constriction is disrupted, compressing force generated by a tissue-level myosin cable contributes to SG invagination. We demonstrate that fully elongated polarized SGs can form outside the embryo, suggesting that tube formation and elongation are intrinsic properties of the SG.
顶端收缩是一种广泛存在的细胞形状变化,与极化上皮的折叠、弯曲和内陷有关。目前尚不清楚在组织内陷过程中顶端收缩是如何在时空上受到调控的,以及这一细胞过程在不同发育背景下如何促进管形成。以唾液腺(SG)内陷为模型,我们发现叉头转录因子对表达的调控是Rho激酶和非肌肉肌球蛋白II在顶内侧积累所必需的,它们共同协调顶端收缩。我们证明,空间协调的顶端收缩的丧失或其完全阻断都不会阻止内化和管形成,尽管这些操作会影响内陷的几何形状。当顶端收缩被破坏时,由组织水平的肌球蛋白索产生的压缩力有助于SG内陷。我们证明,完全伸长的极化SG可以在胚胎外形成,这表明管形成和伸长是SG的内在特性。