IF 14.3 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Science Pub Date : 2025-01-27 DOI:10.1002/advs.202409641
Yiming Leng, Wei Wang, Jun Lu, Jingyuan Chen, Xuliang Chen, Yalan Li, Jie Wang, Yuanyuan Liu, Qian Tan, Wenjing Yang, Youxiang Jiang, Peiyuan Huang, Jingjing Cai, Hong Yuan, Liang Weng, Qingbo Xu, Yao Lu
{"title":"Endothelial TRIM35-Regulated MMP10 Release Exacerbates Calcification of Vascular Grafts.","authors":"Yiming Leng, Wei Wang, Jun Lu, Jingyuan Chen, Xuliang Chen, Yalan Li, Jie Wang, Yuanyuan Liu, Qian Tan, Wenjing Yang, Youxiang Jiang, Peiyuan Huang, Jingjing Cai, Hong Yuan, Liang Weng, Qingbo Xu, Yao Lu","doi":"10.1002/advs.202409641","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":117,"journal":{"name":"Advanced Science","volume":" ","pages":"e2409641"},"PeriodicalIF":14.3000,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/advs.202409641","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

血管钙化是心血管疾病(CVD)的一个高度调节过程,与发病率和死亡率密切相关,尤其是在冠状动脉旁路移植手术(CABG)后血管重塑的不利阶段。然而,血管移植物钙化的发病机制,尤其是内皮细胞与平滑肌细胞相互作用的作用仍不清楚。为了测试动脉移植物中的内皮细胞与平滑肌细胞是如何相互作用的,研究人员首先使用动脉等位移植小鼠模型对野生型小鼠进行了单细胞分析,结果发现细胞因子介导的信号通路激活和平滑肌细胞增殖十分活跃,同时内皮细胞三方基序 35(TRIM35)的表达上调。意想不到的是,在 TRIM35 条件性内皮基因敲除(cKO)小鼠中,动脉移植物中的 SMC 出现了严重的钙化。钙化培养基(由氯化钙和 beta-甘油磷酸酯组成)诱导的体外钙沉积也出现在与 TRIM35 基因敲除内皮共培养的 SMC 中。这一非同寻常的现象被进一步证实是由 MMP10 分泌增加诱导的。从机理上讲,内皮 TRIM35 通过促进 RelB 的 K63 链接泛素化并维持其核定位,从而抑制 MMP10 的表达和分泌,进而通过非正则 NF-κB 信号通路抑制 MMP10 的核转录。在动脉等位移植中原位靶向MMP10能有效缓解条件性内皮TRIM35敲除引起的血管钙化。这些研究结果表明,TRIM35能抑制动脉异位移植重塑过程中的血管钙化,而这一过程是由内皮MMP10的异常分泌驱动的。靶向MMP10通路可能是血管移植物血管钙化的一种潜在治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Endothelial TRIM35-Regulated MMP10 Release Exacerbates Calcification of Vascular Grafts.

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
期刊最新文献
In Situ Analysis of Li Plating and Stripping Behaviors Under Dynamic Current Conditions for Realistic Application Scenarios. Micro-Scale Topography Triggers Dynamic 3D Nuclear Deformations. Peptide-Perovskite Based Bio-Inspired Materials for Optoelectronics Applications. Acid-Triggered Dual-Functional Hydrogel Platform for Enhanced Bone Regeneration. Endothelial TRIM35-Regulated MMP10 Release Exacerbates Calcification of Vascular Grafts.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1