Department of Genetics and Developmental Biology, Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
MERLN Institute for Technology-Inspired Regenerative Medicine, Department of Cell Biology-Inspired Tissue Engineering, Maastricht University, 6200 MD Maastricht, the Netherlands.
Cell Rep. 2024 Mar 26;43(3):113811. doi: 10.1016/j.celrep.2024.113811. Epub 2024 Feb 21.
Extracellular matrix (ECM) rigidity is a major effector of cell fate decisions. Whereas cell proliferation on stiff matrices, wherein Yes-associated protein (YAP) plays a pivotal role, is well documented, activation of apoptosis in response to soft matrices is poorly understood. Here, we show that YAP drives the apoptotic decision as well. We find that in cells on soft matrices, YAP is recruited to small adhesions, phosphorylated at the Y357 residue, and translocated into the nucleus, ultimately leading to apoptosis. In contrast, Y357 phosphorylation levels are dramatically low in large adhesions on stiff matrices. Furthermore, mild attenuation of actomyosin contractility allows adhesion growth on soft matrices, leading to reduced Y357 phosphorylation levels and resulting in cell growth. These findings indicate that failed adhesion reinforcement drives rigidity-dependent apoptosis through YAP and that this decision is not determined solely by ECM rigidity but rather by the balance between cellular forces and ECM rigidity.
细胞外基质(ECM)硬度是细胞命运决定的主要效应因子。尽管在坚硬基质上细胞增殖,其中 Yes 相关蛋白(YAP)起着关键作用,已经有充分的文献记载,但对于软基质中细胞凋亡的激活机制仍知之甚少。在这里,我们表明 YAP 也能驱动细胞凋亡。我们发现,在软基质上的细胞中,YAP 被招募到小黏附物中,在 Y357 残基处发生磷酸化,并转移到细胞核中,最终导致细胞凋亡。相比之下,在坚硬基质上的大黏附物中,Y357 的磷酸化水平极低。此外,轻度减弱肌动球蛋白收缩力可以使细胞在软基质上形成黏附,从而降低 Y357 的磷酸化水平,导致细胞生长。这些发现表明,黏附力减弱导致 YAP 依赖性细胞凋亡,这一决定不仅取决于 ECM 硬度,还取决于细胞力和 ECM 硬度之间的平衡。