Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, 1020 Locust Street, Suite 564, Philadelphia, PA, 19107, USA.
Department of Translational Dental Medicine, School of Dental Medicine, Boston University, 700 Albany Street, W201, Boston, MA, 02118, USA.
Sci Rep. 2021 Jan 11;11(1):330. doi: 10.1038/s41598-020-79650-y.
The development of ductal structures during branching morphogenesis relies on signals that specify ductal progenitors to set up a pattern for the ductal network. Here, we identify cellular asymmetries defined by the F-actin cytoskeleton and the cell adhesion protein ZO-1 as the earliest determinants of duct specification in the embryonic submandibular gland (SMG). Apical polarity protein aPKCζ is then recruited to the sites of asymmetry in a ZO-1-dependent manner and collaborates with ROCK signaling to set up apical-basal polarity of ductal progenitors and further define the path of duct specification. Moreover, the motor protein myosin IIB, a mediator of mechanical force transmission along actin filaments, becomes localized to vertices linking the apical domains of multiple ductal epithelial cells during the formation of ductal lumens and drives duct maturation. These studies identify cytoskeletal, junctional and polarity proteins as the early determinants of duct specification and the patterning of a ductal tree during branching morphogenesis of the SMG.
在分支形态发生过程中,导管结构的发育依赖于指定导管祖细胞的信号,以建立导管网络的模式。在这里,我们确定由 F-肌动蛋白细胞骨架和细胞粘附蛋白 ZO-1 定义的细胞不对称性是胚胎下颌下腺 (SMG) 导管特化的最早决定因素。然后,顶端极性蛋白 aPKCζ 以 ZO-1 依赖的方式被募集到不对称的部位,并与 ROCK 信号合作,建立导管祖细胞的顶端-基底极性,并进一步定义导管特化的路径。此外,肌球蛋白 IIB 是沿肌动蛋白丝传递机械力的运动蛋白,在形成导管腔时,它定位于连接多个导管上皮细胞的顶端区域的顶点,从而驱动导管成熟。这些研究确定了细胞骨架、连接和极性蛋白作为 SMG 分支形态发生过程中导管特化和导管树模式形成的早期决定因素。