Wu Lili, Yang Bo, Sun Yingze, Fan Guanwei, Ma Lina, Ma Ying, Xiong Xianjia, Zhou Hui, Wang Huiping, Zhang Ling, Yang Bing
Department Pathology and Pathophysiology, Logistics University of People's Armed Police Force, Tianjin, 300309, China.
Department of Cardiology, Tianjin Beichen Hospital, Tianjin, 300134, China.
Cardiovasc Toxicol. 2025 Jan;25(1):34-47. doi: 10.1007/s12012-024-09937-3. Epub 2024 Nov 9.
Histone demethylation in cardiac hypertrophy is poorly understood. This study aims to determine the role of the histone demethylase LSD1 in pathological cardiac hypertrophy. Both isoprenaline (ISO)-treated and transverse aortic constriction (TAC)-treated rats developed hypertrophic hearts. LSD1 was significantly decreased; the histone marks mono- and dimethyl H3K4 and H3K9 (H3K4me1/2 and H3K9me1/2) were significantly up-regulated in the hypertrophic heart tissue, as well as the expression of the ANP, α-HMC and MLV-2v genes. An LSD1 inhibitor, OG-L002 could also induce cardiac hypertrophy and enhance the induction of cardiac hypertrophy by ISO. Overexpressed LSD1 abolished ISO-induced cardiac hypertrophy and downregulated H3K4me1/2 and H3K9me1/2 expression. Overexpression of LSD1 also reduced the expression of ANP, α-HMC and MLV-2v. In addition, we have reported isoprenaline (ISO) as one of the histone demethylase LSD1 inhibitors. This was confirmed by molecular docking, molecular dynamic studies and a histone demethylation assay. The H3K4me1/2 expression increases with the incubation of ISO in HEK 293T and HELA cells. CaMKII could be significantly activated by the LSD1 inhibitor OG-L002 as well as by ISO in rats. In summary, we have identified a novel role for LSD1 in initiating and maintaining cardiac hypertrophy.
组蛋白去甲基化在心脏肥大中的作用尚不清楚。本研究旨在确定组蛋白去甲基化酶LSD1在病理性心脏肥大中的作用。用异丙肾上腺素(ISO)处理和经主动脉缩窄(TAC)处理的大鼠均出现心脏肥大。LSD1显著降低;肥大心脏组织中的组蛋白标记单甲基和二甲基H3K4和H3K9(H3K4me1/2和H3K9me1/2)显著上调,以及心房钠尿肽(ANP)、α-心肌肌球蛋白重链(α-HMC)和MLV-2v基因的表达也上调。LSD1抑制剂OG-L002也可诱导心脏肥大,并增强ISO诱导的心脏肥大。过表达LSD1可消除ISO诱导的心脏肥大,并下调H3K4me1/2和H3K9me1/2的表达。LSD1的过表达还降低了ANP、α-HMC和MLV-2v的表达。此外,我们已报道异丙肾上腺素(ISO)是组蛋白去甲基化酶LSD1抑制剂之一。这通过分子对接、分子动力学研究和组蛋白去甲基化测定得到证实。在HEK 293T和HELA细胞中,随着ISO孵育,H3K4me1/2表达增加。在大鼠中,LSD1抑制剂OG-L002以及ISO均可显著激活钙调蛋白依赖性蛋白激酶II(CaMKII)。总之,我们确定了LSD1在启动和维持心脏肥大中的新作用。