Center for Genetic Medicine Research, Children's National Health System, 111 Michigan Avenue, NW, Washington, DC, 20010-2970, USA.
Department of Genomics and Precision Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Cell Mol Life Sci. 2018 Oct;75(20):3751-3770. doi: 10.1007/s00018-018-2888-7. Epub 2018 Jul 26.
Plasma membrane forms the barrier between the cytoplasm and the environment. Cells constantly and selectively transport molecules across their plasma membrane without disrupting it. Any disruption in the plasma membrane compromises its selective permeability and is lethal, if not rapidly repaired. There is a growing understanding of the organelles, proteins, lipids, and small molecules that help cells signal and efficiently coordinate plasma membrane repair. This review aims to summarize how these subcellular responses are coordinated and how cellular signals generated due to plasma membrane injury interact with each other to spatially and temporally coordinate repair. With the involvement of calcium and redox signaling in single cell and tissue repair, we will discuss how these and other related signals extend from single cell repair to tissue level repair. These signals link repair processes that are activated immediately after plasma membrane injury with longer term processes regulating repair and regeneration of the damaged tissue. We propose that investigating cell and tissue repair as part of a continuum of wound repair mechanisms would be of value in treating degenerative diseases.
质膜形成细胞质与环境之间的屏障。细胞不断地、有选择性地将分子运输穿过质膜,而不会破坏质膜。如果不迅速修复,质膜的任何破坏都会损害其选择性通透性,甚至导致细胞死亡。人们越来越了解细胞器、蛋白质、脂质和小分子,它们有助于细胞发出信号并有效地协调质膜修复。本综述旨在总结这些亚细胞反应是如何协调的,以及由于质膜损伤产生的细胞信号如何相互作用,以在空间和时间上协调修复。由于钙和氧化还原信号在单细胞和组织修复中的参与,我们将讨论这些信号以及其他相关信号如何从单细胞修复扩展到组织水平修复。这些信号将在质膜损伤后立即激活的修复过程与调节受损组织修复和再生的长期过程联系起来。我们提出,将细胞和组织修复作为伤口修复机制连续体的一部分进行研究,对于治疗退行性疾病将具有重要价值。