Cell Mechanosensitivity is Enabled by the LINC Nuclear Complex.

Current molecular biology reports Pub Date : 2016-03-01 Epub Date: 2016-02-01 DOI:10.1007/s40610-016-0032-8
Gunes Uzer, Clinton T Rubin, Janet Rubin
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引用次数: 39

Abstract

Mechanoresponses in mesenchymal stem cells (MSCs) guide both differentiation and function. In this review, we focus on advances in0 our understanding of how the cytoplasmic cytoskeleton, nuclear envelope and nucleoskeleton, which are connected via LINC (Linker of Nucleoskeleton and Cytoskeleton) complexes, are emerging as an integrated dynamic signaling platform to regulate MSC mechanobiology. This dynamic interconnectivity affects mechanical signaling and transfer of signals into the nucleus. In this way, nuclear and LINC-mediated cytoskeletal connectivity play a critical role in maintaining mechanical signaling that affects MSC fate by serving as both mechanosensory and mechanoresponsive structures. We review disease and age related compromises of LINC complexes and nucleoskeleton that contribute to the etiology of musculoskeletal diseases. Finally we invite the idea that acquired dysfunctions of LINC might be a contributing factor to conditions such as aging, microgravity and osteoporosis and discuss potential mechanical strategies to modulate LINC connectivity to combat these conditions.

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细胞机械敏感性是由LINC核复合物实现的。
间充质干细胞(MSCs)的机械反应指导分化和功能。在这篇综述中,我们重点介绍了通过LINC(核骨架和细胞骨架的连接物)复合物连接的细胞质细胞骨架、核膜和核骨架如何成为一个综合的动态信号平台来调节MSC的机械生物学。这种动态的相互连接影响机械信号和信号向细胞核的传递。通过这种方式,核和linc介导的细胞骨架连接在维持影响MSC命运的机械信号传导中发挥关键作用,同时作为机械感觉和机械反应结构。我们回顾了与疾病和年龄相关的LINC复合物和核骨架的损害,这些损害有助于肌肉骨骼疾病的病因。最后,我们提出了获得性LINC功能障碍可能是导致衰老、微重力和骨质疏松等疾病的一个因素,并讨论了调节LINC连接以对抗这些疾病的潜在机械策略。
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