Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.
Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.
Curr Biol. 2014 Apr 14;24(8):868-74. doi: 10.1016/j.cub.2014.02.057. Epub 2014 Apr 3.
Apoptotic extrusion is a multicellular process utilized by live cells to remove neighboring apoptotic cells. In epithelial tissues, this process has been shown to be critical for the preservation of tissue integrity and barrier function. Here we demonstrate that extrusion is driven by the retraction of the apoptotic cell, which, in turn, triggers a transient and coordinated elongation of the neighboring cells. The coordination of cell elongation requires E-cadherin-mediated cell-cell adhesion. Accordingly, cells that express low levels of E-cadherin are compromised in elongation and apoptotic extrusion, and furthermore, display loss of barrier function in response to apoptotic stimuli. These findings indicate that the maintenance of adhesive forces during apoptotic cell turnover might play an essential role in controlling tissue homeostasis.
细胞凋亡挤出是活细胞用来清除邻近凋亡细胞的一种细胞多形性过程。在上皮组织中,该过程对于维持组织完整性和屏障功能至关重要。在这里,我们证明挤出是由凋亡细胞的回缩驱动的,反过来,凋亡细胞的回缩又触发了邻近细胞的短暂和协调伸长。细胞伸长的协调需要 E-钙黏蛋白介导的细胞间黏附。因此,表达低水平 E-钙黏蛋白的细胞在伸长和凋亡挤出方面受到影响,并且在受到凋亡刺激时显示出屏障功能丧失。这些发现表明,在凋亡细胞更替过程中维持黏附力可能在控制组织动态平衡中发挥重要作用。