乳酸盐通过 H3K14la/KLF5 通路驱动糖尿病肾病的上皮-间质转化

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xuanxuan Zhang , Jicong Chen , Ruohui Lin , Yaping Huang , Ziyuan Wang , Susu Xu , Lei Wang , Fang Chen , Jian Zhang , Ke Pan , Zhiqi Yin
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引用次数: 0

摘要

高水平的尿乳酸盐会增加糖尿病肾病(DKD)患者病情恶化的风险。然而,乳酸盐是如何驱动糖尿病肾病的,目前仍是个未知数。上皮-间质转化(EMT)的特点是上皮细胞极性和细胞-细胞粘附性的丧失,以及间质样表型的获得,被广泛认为是导致 DKD 的关键因素。在这里,我们发现 AGE 诱导的肾小管上皮细胞从氧化磷酸化(OXPHOS)转向糖酵解,从而导致肾乳酸水平升高。我们证实,降低乳酸水平可明显延缓 DKD 的 EMT 进展并改善肾小管纤维化。在机制上,我们观察到乳酸增加了 DKD 中组蛋白 H3 赖氨酸 14 乳酰化(H3K14la)的水平。ChIP-seq和RNA-seq结果显示,组蛋白乳酸化通过促进KLF5的表达,推动了EMT过程。此外,KLF5能识别cdh1的启动子并抑制其转录,从而加速了DKD的EMT。此外,肾特异性敲除和药物抑制KLF5可减少EMT的发展,减轻DKD纤维化。因此,我们的研究有助于更好地理解DKD发病机制的表观遗传调控,并通过破坏乳酸驱动的H3K14la/KLF5通路为DKD提供新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lactate drives epithelial-mesenchymal transition in diabetic kidney disease via the H3K14la/KLF5 pathway

Lactate drives epithelial-mesenchymal transition in diabetic kidney disease via the H3K14la/KLF5 pathway

Lactate drives epithelial-mesenchymal transition in diabetic kidney disease via the H3K14la/KLF5 pathway

High levels of urinary lactate are an increased risk of progression in patients with diabetic kidney disease (DKD). However, it is still unveiled how lactate drive DKD. Epithelial-mesenchymal transition (EMT), which is characterized by the loss of epithelial cells polarity and cell-cell adhesion, and the acquisition of mesenchymal-like phenotypes, is widely recognized a critical contributor to DKD. Here, we found a switch from oxidative phosphorylation (OXPHOS) toward glycolysis in AGEs-induced renal tubular epithelial cells, thus leading to elevated levels of renal lactic acid. We demonstrated that reducing the lactate levels markedly delayed EMT progression and improved renal tubular fibrosis in DKD. Mechanically, we observed lactate increased the levels of histone H3 lysine 14 lactylation (H3K14la) in DKD. ChIP-seq & RNA-seq results showed histone lactylation contributed to EMT process by facilitating KLF5 expression. Moreover, KLF5 recognized the promotor of cdh1 and inhibited its transcription, which accelerated EMT of DKD. Additionally, nephro-specific knockdown and pharmacological inhibition of KLF5 diminished EMT development and attenuated DKD fibrosis. Thus, our study provides better understanding of epigenetic regulation of DKD pathogenesis, and new therapeutic strategy for DKD by disruption of the lactate-drived H3K14la/KLF5 pathway.

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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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