Department of Chemical Engineering, University of Florida, Gainesville, FL 32611, USA.
Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA.
Curr Biol. 2019 Sep 9;29(17):2826-2839.e4. doi: 10.1016/j.cub.2019.07.021. Epub 2019 Aug 8.
The nucleoskeleton and cytoskeleton are important protein networks that govern cellular behavior and are connected together by the linker of nucleoskeleton and cytoskeleton (LINC) complex. Mutations in LINC complex components may be relevant to cancer, but how cell-level changes might translate into tissue-level malignancy is unclear. We used glandular epithelial cells in a three-dimensional culture model to investigate the effect of perturbations of the LINC complex on higher order cellular architecture. We show that inducible LINC complex disruption in human mammary epithelial MCF-10A cells and canine kidney epithelial MDCK II cells mechanically destabilizes the acinus. Lumenal collapse occurs because the acinus is unstable to increased mechanical tension that is caused by upregulation of Rho-kinase-dependent non-muscle myosin II motor activity. These findings provide a potential mechanistic explanation for how disruption of LINC complex may contribute to a loss of tissue structure in glandular epithelia.
核骨架和细胞骨架是重要的蛋白质网络,它们控制着细胞的行为,并通过核骨架-细胞骨架连接蛋白(LINC)复合体连接在一起。LINC 复合体成分的突变可能与癌症有关,但细胞水平的变化如何转化为组织水平的恶性肿瘤尚不清楚。我们使用三维培养模型中的腺上皮细胞来研究 LINC 复合体的扰动对更高阶细胞结构的影响。我们表明,在人乳腺上皮 MCF-10A 细胞和犬肾上皮 MDCK II 细胞中诱导的 LINC 复合体破坏会使腺泡在机械上不稳定。管腔塌陷是因为腺泡不稳定,无法承受 Rho-激酶依赖性非肌肉肌球蛋白 II 运动活性上调引起的机械张力增加。这些发现为 LINC 复合体的破坏如何导致腺上皮组织结构丧失提供了潜在的机制解释。