Department of Molecular Biosciences, Rice Institute for Biomedical Research, Northwestern University, Evanston, IL 60208, USA.
J Exp Biol. 2014 Jan 1;217(Pt 1):129-36. doi: 10.1242/jeb.091249.
The ability of each cell within a metazoan to adapt to and survive environmental and physiological stress requires cellular stress-response mechanisms, such as the heat shock response (HSR). Recent advances reveal that cellular proteostasis and stress responses in metazoans are regulated by multiple layers of intercellular communication. This ensures that an imbalance of proteostasis that occurs within any single tissue 'at risk' is protected by a compensatory activation of a stress response in adjacent tissues that confers a community protective response. While each cell expresses the machinery for heat shock (HS) gene expression, the HSR is regulated cell non-autonomously in multicellular organisms, by neuronal signaling to the somatic tissues, and by transcellular chaperone signaling between somatic tissues and from somatic tissues to neurons. These cell non-autonomous processes ensure that the organismal HSR is orchestrated across multiple tissues and that transmission of stress signals between tissues can also override the neuronal control to reset cell- and tissue-specific proteostasis. Here, we discuss emerging concepts and insights into the complex cell non-autonomous mechanisms that control stress responses in metazoans and highlight the importance of intercellular communication for proteostasis maintenance in multicellular organisms.
真核生物中每个细胞适应和生存环境及生理压力的能力需要细胞应激反应机制,如热休克反应(HSR)。最近的进展表明,真核生物的细胞蛋白稳态和应激反应受多层次的细胞间通讯调控。这确保了发生在任何单个“有风险”组织中的蛋白稳态失衡受到相邻组织中应激反应的代偿性激活的保护,从而赋予了社区保护反应。虽然每个细胞都表达了热休克(HS)基因表达的机制,但在多细胞生物中,HSR 是通过神经元信号传递到体组织,以及通过体细胞组织之间的伴侣蛋白信号传递和从体细胞组织到神经元的信号传递,以非自主的方式进行调节的。这些非自主细胞过程确保了生物体 HSR 在多个组织中协调,并强调了细胞间通讯对于维持多细胞生物中蛋白稳态的重要性。在这里,我们讨论了控制真核生物应激反应的复杂非自主细胞机制的新出现的概念和见解,并强调了细胞间通讯对于维持多细胞生物中蛋白稳态的重要性。