Lin Ling, Hu Kebin
Department of Medicine and Department of Cell and Biological Systems, The Pennsylvania State University College of Medicine, Hershey, PA, United States.
Front Cell Dev Biol. 2025 Jun 5;13:1593914. doi: 10.3389/fcell.2025.1593914. eCollection 2025.
The 90 kDa ribosomal s6 kinases (RSKs) are a group of serine/threonine kinases consisting of 4 RSK isoforms (RSK1-4), of which RSK1 is also named as p90RSK. p90RSK is directly phosphorylated and activated by its immediate upstream mediator extracellular signal-regulated kinase (Erk1/2), followed by activating various signaling pathways through phosphorylating selective downstream substrates. Aberrant induction of p90RSK has been reported in various human diseases including kidney disease suggesting a pathogenic role of p90RSK in these diseases. In response to pathogenic cues, p90RSK not only mediates intracellular signal events leading to cell-specific phenotypes but also modulates intercellular communication impacting the adjacent cellular responses. In this review, we provide an update on the current knowledge regarding the roles of p90RSK-mediated intercellular and intracellular signaling in the pathogenesis and progression of kidney diseases.
90 kDa核糖体S6激酶(RSKs)是一组丝氨酸/苏氨酸激酶,由4种RSK亚型(RSK1 - 4)组成,其中RSK1也被称为p90RSK。p90RSK被其紧邻的上游介质细胞外信号调节激酶(Erk1/2)直接磷酸化并激活,随后通过磷酸化选择性下游底物激活各种信号通路。在包括肾脏疾病在内的各种人类疾病中,均已报道p90RSK的异常诱导,提示p90RSK在这些疾病中具有致病作用。响应致病信号,p90RSK不仅介导导致细胞特异性表型的细胞内信号事件,还调节影响相邻细胞反应的细胞间通讯。在本综述中,我们提供了关于p90RSK介导的细胞间和细胞内信号在肾脏疾病发病机制和进展中的作用的当前知识更新。