Ghrelin Alleviates Aging-Related Cognitive Impairment by Regulating Autophagy-Related Signaling via the SHBG/JNK1/Beclin1 Axis in Microglia

IF 7.7 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Aging Cell Pub Date : 2026-09-29 DOI:10.1111/acel.70732
Lixing Zhou, Ying Cheng, Wanyu Zhao, Xuelian Sun, Fengjuan Hu, Meiling Ge, Yan Zhang, Gongchang Zhang, Birong Dong, Xiaolei Liu
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Abstract

Cognitive impairment (CI) associated with aging and immunosenescence is linked to metabolic alterations. Microglial senescence and dysregulated autophagy have been implicated as major contributors to this process, but the underlying metabolic regulators remain unclear. This study aimed to identify key metabolic regulators of CI and elucidate their underlying mechanisms. Human cohort analyses, older and D-galactose (D-gal)-induced mouse models, and microglial cell models were integrated to investigate the metabolic regulation of CI. Clinical analyses identified ghrelin as the factor most strongly associated with CI. Older and D-gal mice exhibited CI, microglial senescence, enhanced inflammation, and elevated ghrelin. Ghrelin treatment improved cognitive function, attenuated microglial senescence, and suppressed inflammation, whereas high-dose ghrelin induced growth hormone secretagogue receptor (GHSR) desensitization. Sex hormone-binding globulin (SHBG) showed mainly cytoplasmic localization, was identified as a potential mediator of ghrelin signaling in microglia, and its expression was downregulated following ghrelin treatment. Transcriptomic profiling revealed significant enrichment of autophagy-related pathways in ghrelin-treated microglia. Ghrelin altered autophagy-related markers, as indicated by increased Beclin1 and LC3 and decreased p62. SHBG overexpression or JNK1 inhibition attenuated the ghrelin-induced alterations in autophagy-related markers and anti-senescent effects, whereas Beclin1 overexpression partially rescued these inhibitory effects caused by SHBG overexpression. In conclusion, ghrelin alleviated aging-related CI, with mechanistic evidence indicating that the modulation of microglial autophagy-related mechanisms through the SHBG/JNK1/Beclin1 axis may contribute to its protective effects, thereby providing a potential therapeutic strategy for aging-related CI.

Ghrelin通过小胶质细胞SHBG/JNK1/Beclin1轴调节自噬相关信号通路减轻衰老相关认知障碍
与衰老和免疫衰老相关的认知障碍(CI)与代谢改变有关。小胶质细胞衰老和失调的自噬被认为是这一过程的主要贡献者,但潜在的代谢调节因子尚不清楚。本研究旨在确定CI的关键代谢调节因子并阐明其潜在机制。结合人类队列分析、老年和d -半乳糖(D-gal)诱导的小鼠模型以及小胶质细胞模型来研究CI的代谢调节。临床分析确定胃饥饿素是与CI最密切相关的因素。老年小鼠和D-gal小鼠表现出CI、小胶质细胞衰老、炎症增强和胃饥饿素升高。胃饥饿素治疗改善认知功能,减轻小胶质细胞衰老,抑制炎症,而高剂量胃饥饿素诱导生长激素分泌受体(GHSR)脱敏。性激素结合球蛋白(Sex hormone-binding globulin, SHBG)主要表现为细胞质定位,被认为是小胶质细胞中胃饥饿素信号传导的潜在介质,在胃饥饿素治疗后其表达下调。转录组学分析显示,在胃饥饿素处理的小胶质细胞中,自噬相关通路显著富集。Ghrelin改变了自噬相关的标志物,Beclin1和LC3升高,p62降低。SHBG过表达或JNK1抑制会减弱ghrelin诱导的自噬相关标志物的改变和抗衰老作用,而Beclin1过表达部分地恢复了SHBG过表达引起的这些抑制作用。综上所述,ghrelin减轻了衰老相关的CI,机制证据表明,通过SHBG/JNK1/Beclin1轴调节小胶质细胞自噬相关机制可能有助于其保护作用,从而为衰老相关的CI提供了潜在的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
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