Chen Michelle X, Oh Yong-Seok, Kim Yong
University of Iowa Medical Scientist Training Program, Carver College of Medicine, University of Iowa, Iowa, IA, United States.
Department of Brain Sciences, Daegu-Gyeongbuk Institute of Science and Technology (DGIST), Daegu, South Korea.
Front Mol Neurosci. 2022 Aug 15;15:953066. doi: 10.3389/fnmol.2022.953066. eCollection 2022.
S100A10 (p11) is an emerging player in the neurobiology of depression and antidepressant actions. p11 was initially thought to be a modulator of serotonin receptor (5-HTR) trafficking and serotonergic transmission, though newly identified binding partners of p11 and neurobiological studies of these proteins have shed light on multifunctional roles for p11 in the regulation of glutamatergic transmission, calcium signaling and nuclear events related to chromatin remodeling, histone modification, and gene transcription. This review article focuses on direct binding partners of p11 in the brain including 5-HTRs, mGluR5, annexin A2, Ahnak, Smarca3, and Supt6h, as well as their roles in neuronal function, particularly in the context of depressive-like behavior as well as behavioral effects of antidepressant drug treatments in mice. In addition, we discuss neurobiological insights from recently uncovered p11 pathways in multiple types of neurons and non-neuronal cells and cast major remaining questions for future studies.
S100A10(p11)在抑郁症神经生物学及抗抑郁作用中是一个新出现的相关因素。p11最初被认为是血清素受体(5 - HTR)转运和血清素能传递的调节剂,不过p11新确定的结合伴侣以及对这些蛋白质的神经生物学研究揭示了p11在谷氨酸能传递调节、钙信号传导以及与染色质重塑、组蛋白修饰和基因转录相关的核事件中的多功能作用。这篇综述文章重点关注p11在大脑中的直接结合伴侣,包括5 - HTRs、代谢型谷氨酸受体5(mGluR5)、膜联蛋白A2、Ahnak、Smarca3和Supt6h,以及它们在神经元功能中的作用,特别是在小鼠抑郁样行为以及抗抑郁药物治疗的行为效应方面。此外,我们讨论了最近在多种类型的神经元和非神经元细胞中发现的p11途径的神经生物学见解,并提出了未来研究中主要的遗留问题。