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补肾活血针刺通过上调 MARCHF3 诱导 NLRP3 泛素化,抑制 caspase-1 依赖性细胞焦亡来改善阿尔茨海默病。

Bushen Huoxue acupuncture ameliorates Alzheimer's disease by upregulating MARCHF3 to induce NLRP3 ubiquitination and inhibit caspase-1-dependent pyroptosis.

机构信息

Department of Traditional Chinese Medicine, The Third Xiangya Hospital of Central South University, 138 Tongzipo Road, Changsha, 410008, Hunan Province, China.

出版信息

Metab Brain Dis. 2024 Nov 18;40(1):11. doi: 10.1007/s11011-024-01459-9.

Abstract

Alzheimer's disease (AD) is a common neurodegenerative disorder that places a heavy burden on patients and society. Hippocampal neuronal loss is a hallmark of AD progression. Therefore, understanding the mechanism underlying hippocampal neuronal death would be of great importance for the diagnosis and treatment of AD. This study aimed to explore the molecular mechanism via which Bushen Huoxue Acupuncture inhibits hippocampal neuronal pyroptosis in AD. Senescence-accelerated mouse prone 8 (SAMP8) mice were used as a model of AD. Bushen Huoxue Acupuncture was performed in four acupoints: "Baihui acupoint" (GV20), "Shenshu acupoint" (BL23), "Xuehai acupoint" (SP10), and "Geshu acupoint" (BL17). Morris water maze was used to test cognitive function in mice. IHC staining was used to test mice's Aβ1-42, MARCHF1 and MARCHF3 expression. Terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) staining was used for observing hippocampal neuronal apoptosis. The mRNA expression levels of pyroptosis markers MARCHF1, MARCHF3, NLRP3, caspase-1, GSDMD, IL-1β, and IL-18 mRNA in AD mice were determined by quantitative reverse transcription polymerase chain reaction (qRT-PCR). The protein expression of NLRP3, caspase-1 and GSDMD-N was tested by Western blotting. IL-1β and IL-18 protein levels were measured by Enzyme-Linked Immunosorbent Assay (ELISA). SH-SY5Y cells were used to establish an AD model following Aβ treatment. Western blot was used to detect the NLRP3, MARCHF1 and MARCHF3 proteins following Aβ treatment. The endogenous Co-IP assay in combination with immunoblotting for ubiquitin signals was used to detect of NLRP3 ubiquitination level. We found that Bushen Huoxue Acupuncture protected cognitive impairment in AD mice. Bushen Huoxue Acupuncture inhibited hippocampal neuronal pyroptosis and the secretion of inflammatory cytokines in vivo. In SH-SY5Y cells, we found that Aβ decreased the binding of E3 ubiquitin-protein ligase MARCHF1 or MARCHF3 with NLRP3, and the ubiquitination of NLRP3. In conclusion, Bushen Huoxue Acupuncture ameliorates AD by upregulating MARCHF3 to induce NLRP3 ubiquitination and inhibits caspase-1-dependent pyroptosis.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病,给患者和社会带来了沉重的负担。海马神经元丢失是 AD 进展的标志。因此,了解海马神经元死亡的机制对于 AD 的诊断和治疗具有重要意义。本研究旨在探讨补肾活血针刺通过抑制 AD 中海马神经元细胞焦亡的分子机制。衰老加速小鼠品系 8(SAMP8)小鼠被用作 AD 模型。在四个穴位进行补肾活血针刺:“百会穴”(GV20)、“肾俞穴”(BL23)、“血海穴”(SP10)和“膈俞穴”(BL17)。使用 Morris 水迷宫测试小鼠的认知功能。免疫组织化学染色用于检测小鼠的 Aβ1-42、MARCHF1 和 MARCHF3 表达。末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)染色用于观察海马神经元凋亡。通过定量逆转录聚合酶链反应(qRT-PCR)测定 AD 小鼠中细胞焦亡标志物 MARCHF1、MARCHF3、NLRP3、caspase-1、GSDMD、IL-1β和 IL-18mRNA 的表达水平。通过 Western blot 检测 NLRP3、caspase-1 和 GSDMD-N 蛋白的表达。通过酶联免疫吸附测定(ELISA)测量 IL-1β和 IL-18 蛋白水平。用 Aβ 处理 SH-SY5Y 细胞建立 AD 模型。用 Western blot 检测 Aβ 处理后 NLRP3、MARCHF1 和 MARCHF3 蛋白的表达。用内源性 Co-IP 测定结合免疫印迹检测泛素信号,检测 NLRP3 泛素化水平。我们发现补肾活血针刺可保护 AD 小鼠的认知障碍。补肾活血针刺可抑制体内海马神经元细胞焦亡和炎症细胞因子的分泌。在 SH-SY5Y 细胞中,我们发现 Aβ 降低了 E3 泛素蛋白连接酶 MARCHF1 或 MARCHF3 与 NLRP3 的结合,以及 NLRP3 的泛素化。综上所述,补肾活血针刺通过上调 MARCHF3 诱导 NLRP3 泛素化,抑制 caspase-1 依赖性细胞焦亡,改善 AD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6789/11573812/f06f6b919270/11011_2024_1459_Fig1_HTML.jpg

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