肾脏脂质积累和衰老与肾小管细胞通过 ANGPTL4 受损有关

IF 5.3 3区 医学 Q2 CELL BIOLOGY
Xiaojun Wang , Hung-chen Chang , Xuchao Gu , Wanlin Han , Shihang Mao , Lili Lu , Shuai Jiang , Haiyong Ding , Shisheng Han , Xinkai Qu , Zhijun Bao
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引用次数: 0

摘要

肾小管上皮细胞很容易受到压力引起的损伤,包括过度脂质积累和衰老,而 ANGPTL4 可能在这些因素之间起着关键的桥梁作用。本研究利用 RNA 测序技术发现,在饮食诱导的肥胖和衰老小鼠肾脏中,ANGPTL4 的表达明显增加。研究人员利用肾小管上皮细胞(HK-2)中 ANGPTL4 的过表达和基因敲除来研究其潜在机制。随后,利用酶联免疫吸附和免疫组化技术分析了ANGPTL4在正常年轻对照组和老年人血浆和肾组织中的表达。RNA测序结果显示,ANGPTL4在饮食诱导肥胖和衰老小鼠肾组织中的表达明显上调。体外实验表明,在 HK-2 细胞中过表达 ANGPTL4 会导致脂质沉积增加和衰老。相反,ANGPTL4的缺失似乎减轻了游离脂肪酸(FFA)对HK-2细胞衰老的影响。此外,衰老的 HK-2 细胞表现出 ANGPTL4 表达的升高,以及与细胞周期停滞相关的应激反应标记。此外,我们的临床证据显示,与年轻人相比,老年人的血清和肾组织样本中 ANGPTL4 表达失调。我们的研究结果表明,ANGPTL4 与年龄相关的代谢紊乱以及肾小管上皮细胞损伤之间存在潜在联系。这表明,靶向 ANGPTL4 可能是临床治疗肾脏衰老的一种可行策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Renal lipid accumulation and aging linked to tubular cells injury via ANGPTL4

Renal lipid accumulation and aging linked to tubular cells injury via ANGPTL4

Renal tubular epithelial cells are vulnerable to stress-induced damage, including excessive lipid accumulation and aging, with ANGPTL4 potentially playing a crucial bridging role between these factors. In this study, RNA-sequencing was used to identify a marked increase in ANGPTL4 expression in kidneys of diet-induced obese and aging mice. Overexpression and knockout of ANGPTL4 in renal tubular epithelial cells (HK-2) was used to investigate the underlying mechanism. Subsequently, ANGPTL4 expression in plasma and kidney tissues of normal young controls and elderly individuals was analyzed using ELISA and immunohistochemical techniques. RNA sequencing results showed that ANGPTL4 expression was significantly upregulated in the kidney tissue of diet-induced obesity and aging mice. In vitro experiments demonstrated that overexpression of ANGPTL4 in HK-2 cells led to increased lipid deposition and senescence. Conversely, the absence of ANGPTL4 appears to alleviate the impact of free fatty acids (FFA) on aging in HK-2 cells. Additionally, aging HK-2 cells exhibited elevated ANGPTL4 expression, and stress response markers associated with cell cycle arrest. Furthermore, our clinical evidence revealed dysregulation of ANGPTL4 expression in serum and kidney tissue samples obtained from elderly individuals compared to young subjects. Our study findings indicate a potential association between ANGPTL4 and age-related metabolic disorders, as well as injury to renal tubular epithelial cells. This suggests that targeting ANGPTL4 could be a viable strategy for the clinical treatment of renal aging.

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来源期刊
CiteScore
11.10
自引率
1.90%
发文量
79
审稿时长
32 days
期刊介绍: Mechanisms of Ageing and Development is a multidisciplinary journal aimed at revealing the molecular, biochemical and biological mechanisms that underlie the processes of aging and development in various species as well as of age-associated diseases. Emphasis is placed on investigations that delineate the contribution of macromolecular damage and cytotoxicity, genetic programs, epigenetics and genetic instability, mitochondrial function, alterations of metabolism and innovative anti-aging approaches. For all of the mentioned studies it is necessary to address the underlying mechanisms. Mechanisms of Ageing and Development publishes original research, review and mini-review articles. The journal also publishes Special Issues that focus on emerging research areas. Special issues may include all types of articles following peered review. Proposals should be sent directly to the Editor-in-Chief.
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