Leng Yiming, Wang Wei, Lu Jun, Chen Jingyuan, Chen Xuliang, Li Yalan, Wang Jie, Liu Yuanyuan, Tan Qian, Yang Wenjing, Jiang Youxiang, Huang Peiyuan, Cai Jingjing, Yuan Hong, Weng Liang, Xu Qingbo, Lu Yao
Clinical Research Center, Postdoctoral Station of Clinical Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, P. R. China.
Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, P. R. China.
Adv Sci (Weinh). 2025 Mar;12(11):e2409641. doi: 10.1002/advs.202409641. Epub 2025 Jan 27.
Vascular calcification is a highly regulated process in cardiovascular disease (CVD) and is strongly correlated with morbidity and mortality, especially in the adverse stage of vascular remodeling after coronary artery bypass graft surgery (CABG). However, the pathogenesis of vascular graft calcification, particularly the role of endothelial-smooth muscle cell interaction, is still unclear. To test how ECs interact with SMCs in artery grafts, single-cell analysis of wild-type mice is first performed using an arterial isograft mouse model and found robust cytokine-mediated signaling pathway activation and SMC proliferation, together with upregulated endothelial tripartite motif 35 (TRIM35) expression. Unexpectedly, severe SMC calcification in artery grafts is found in TRIM35 conditional endothelial knockout (cKO) mice. Calcified medium (comprising calcium chloride and beta-glycerophosphate)-induced calcium deposition in vitro is also found in SMCs cocultured with TRIM35 knockout endothelium. This extraordinary phenomenon is further confirmed to be induced by increased MMP10 secretion. Mechanistically, endothelial TRIM35 inhibits MMP10 expression and secretion by promoting K63-linked ubiquitination of RelB and maintaining its nuclear localization, consequently inhibiting nuclear transcription of MMP10 through the noncanonical NF-κB signaling pathway. Targeting MMP10 in situ in arterial isografts can effectively alleviate vascular calcification caused by conditional endothelial TRIM35 knockout. These findings demonstrated that TRIM35 inhibited vascular calcification during arterial isograft remodeling, a process that is driven by the aberrant secretion of endothelial MMP10. Targeting MMP10 pathway may be a potential therapeutic strategy for vascular calcification in vessel grafts.
血管钙化是心血管疾病(CVD)中一个高度受调控的过程,与发病率和死亡率密切相关,尤其是在冠状动脉旁路移植术(CABG)后血管重塑的不良阶段。然而,血管移植物钙化的发病机制,特别是内皮细胞与平滑肌细胞相互作用的作用,仍不清楚。为了测试内皮细胞(ECs)与动脉移植物中的平滑肌细胞(SMCs)如何相互作用,首先使用动脉同基因移植小鼠模型对野生型小鼠进行单细胞分析,发现有强大的细胞因子介导的信号通路激活和平滑肌细胞增殖,同时内皮三联基序35(TRIM35)表达上调。出乎意料的是,在TRIM35条件性内皮敲除(cKO)小鼠的动脉移植物中发现了严重的平滑肌细胞钙化。在与TRIM35敲除内皮共培养的平滑肌细胞中,还发现钙化培养基(包含氯化钙和β-甘油磷酸)在体外诱导钙沉积。这种异常现象进一步证实是由MMP10分泌增加所诱导。机制上,内皮TRIM35通过促进RelB的K63连接泛素化并维持其核定位来抑制MMP10的表达和分泌,从而通过非经典NF-κB信号通路抑制MMP10的核转录。在动脉同基因移植物中原位靶向MMP10可有效减轻由条件性内皮TRIM35敲除引起的血管钙化。这些发现表明,TRIM35在动脉同基因移植重塑过程中抑制血管钙化,这一过程由内皮MMP10的异常分泌驱动。靶向MMP10通路可能是血管移植物中血管钙化的一种潜在治疗策略。