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非基因组机制介导雄激素诱导的PSD95表达。

Non-genomic mechanisms mediate androgen-induced PSD95 expression.

作者信息

Zhang Yizhou, Li Sha, Chen Huan, Chen Meiqin, Mi Shixiong, Ma Jingle, Wang Chang, Sun Hongmei, Liu Xiaoyun, Cui Huixian

机构信息

Department of Anatomy, Hebei Medical University, Shijiazhuang, China.

Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.

出版信息

Aging (Albany NY). 2019 Apr 20;11(8):2281-2294. doi: 10.18632/aging.101913.

Abstract

The non-genomic actions of androgen-induced synaptic plasticity have been extensively studied. However, the underlying mechanisms remain controversial. We recently found that testosterone-fetal bovine serum albumin (T-BSA), a cell membrane-impermeable complex, led to a rapid increase in the postsynaptic density 95 (PSD95) protein level through a transcription-independent mechanism in mouse hippocampal HT22 cells. Using T-BSA conjugated FITC, we verified the presence of membrane androgen-binding sites. Here, we show that T-BSA-induced PSD95 expression is mediated by G-protein-coupled receptor (GPCR)-zinc transporter ZIP9 (SLC39A9), one of the androgen membrane binding sites, rather than the membrane-localized androgen receptor. Furthermore, we found that T-BSA induced an interaction between ZIP9 and Gnα11 that lead to the phosphorylation of Erk1/2 MAPK and eIF4E, which are critical in the mRNA translation process. The PSD95 and p-eIF4E expression decreased when knockdown of ZIP9 or Gnα11 expression or inhibition of Erk1/2 activation. Taken together, these findings suggest that ZIP9 mediates the non-genomic action of androgen on synaptic protein PSD95 synthesis through the Gnα11/Erk1/2/eIF4E pathway in HT22 cells. This novel mechanism provides a theoretical basis to understand the neuroprotective mechanism of androgen.

摘要

雄激素诱导的突触可塑性的非基因组作用已得到广泛研究。然而,其潜在机制仍存在争议。我们最近发现,睾酮 - 胎牛血清白蛋白(T - BSA),一种不能透过细胞膜的复合物,通过一种不依赖转录的机制,导致小鼠海马HT22细胞中突触后致密蛋白95(PSD95)水平迅速升高。使用与异硫氰酸荧光素(FITC)偶联的T - BSA,我们证实了膜雄激素结合位点的存在。在此,我们表明,T - BSA诱导的PSD95表达是由G蛋白偶联受体(GPCR) - 锌转运体ZIP9(SLC39A9)介导的,ZIP9是雄激素膜结合位点之一,而非膜定位的雄激素受体。此外,我们发现T - BSA诱导ZIP9与Gnα11之间相互作用,导致细胞外信号调节激酶1/2(Erk1/2)丝裂原活化蛋白激酶和真核翻译起始因子4E(eIF4E)磷酸化,这在mRNA翻译过程中至关重要。当ZIP9或Gnα11表达敲低或Erk1/2激活受到抑制时,PSD95和磷酸化eIF4E表达下降。综上所述,这些发现表明,ZIP9通过HT22细胞中的Gnα11/Erk1/2/eIF4E途径介导雄激素对突触蛋白PSD95合成的非基因组作用。这一新机制为理解雄激素的神经保护机制提供了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/999d/6520003/d412862aab3d/aging-11-101913-g001.jpg

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