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ROCK1 定向基底膜定位协调上皮组织极性。

ROCK1-directed basement membrane positioning coordinates epithelial tissue polarity.

机构信息

Graduate program in Molecular, Cellular, Developmental, and Neural Biology, University at Albany, State University of New York, Albany, NY 12208, USA.

出版信息

Development. 2012 Jan;139(2):411-22. doi: 10.1242/dev.075366.

Abstract

The basement membrane is crucial for epithelial tissue organization and function. However, the mechanisms by which basement membrane is restricted to the basal periphery of epithelial tissues and the basement membrane-mediated signals that regulate coordinated tissue organization are not well defined. Here, we report that Rho kinase (ROCK) controls coordinated tissue organization by restricting basement membrane to the epithelial basal periphery in developing mouse submandibular salivary glands, and that ROCK inhibition results in accumulation of ectopic basement membrane throughout the epithelial compartment. ROCK-regulated restriction of PAR-1b (MARK2) localization in the outer basal epithelial cell layer is required for basement membrane positioning at the tissue periphery. PAR-1b is specifically required for basement membrane deposition, as inhibition of PAR-1b kinase activity prevents basement membrane deposition and disrupts overall tissue organization, and suppression of PAR-1b together with ROCK inhibition prevents interior accumulations of basement membrane. Conversely, ectopic overexpression of wild-type PAR-1b results in ectopic interior basement membrane deposition. Significantly, culture of salivary epithelial cells on exogenous basement membrane rescues epithelial organization in the presence of ROCK1 or PAR-1b inhibition, and this basement membrane-mediated rescue requires functional integrin β1 to maintain epithelial cell-cell adhesions. Taken together, these studies indicate that ROCK1/PAR-1b-dependent regulation of basement membrane placement is required for the coordination of tissue polarity and the elaboration of tissue structure in the developing submandibular salivary gland.

摘要

基膜对于上皮组织的结构和功能至关重要。然而,基膜被限制在上皮组织基底面的机制,以及基膜介导的调节组织协调的信号,尚不完全清楚。在这里,我们报告 Rho 激酶(ROCK)通过将基膜限制在发育中的小鼠颌下唾液腺的上皮基底面来控制组织的协调,ROCK 抑制导致基膜在整个上皮细胞区室中积累异位。ROCK 调节的 PAR-1b(MARK2)在基底上皮细胞层的外层的定位限制对于基膜在组织边缘的定位是必需的。PAR-1b 是基膜沉积所必需的,因为 PAR-1b 激酶活性的抑制会阻止基膜沉积并破坏整体组织结构,而 PAR-1b 的抑制与 ROCK 抑制一起可防止基膜在内层的积累。相反,野生型 PAR-1b 的异位过表达会导致基膜在内部的异位沉积。重要的是,在 ROCK1 或 PAR-1b 抑制的情况下,唾液腺上皮细胞在细胞外基膜上的培养可挽救上皮组织的结构,而这种基膜介导的挽救需要功能性整合素β1 来维持上皮细胞-细胞间的粘附。总之,这些研究表明,ROCK1/PAR-1b 依赖性基膜定位的调节对于下颌下唾液腺发育中组织极性的协调和组织结构的形成是必需的。

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