Extensive Proliferation of a Subset of Differentiated, yet Plastic, Medial Vascular Smooth Muscle Cells Contributes to Neointimal Formation in Mouse Injury and Atherosclerosis Models

血管平滑肌 平滑肌 新生内膜 心脏病学 解剖 医学 细胞生物学 病理 内科学 生物 再狭窄 支架
作者
Joel Chappell,Jennifer Jill Harman,Vagheesh M. Narasimhan,Haixiang Yu,Kirsty Foote,Benjamin D. Simons,Martin R. Bennett,Helle Færk Jørgensen
出处
期刊:Circulation Research [Lippincott Williams & Wilkins]
卷期号:119 (12): 1313-1323 被引量:437
标识
DOI:10.1161/circresaha.116.309799
摘要

RATIONALE: Vascular smooth muscle cell (VSMC) accumulation is a hallmark of atherosclerosis and vascular injury. However, fundamental aspects of proliferation and the phenotypic changes within individual VSMCs, which underlie vascular disease, remain unresolved. In particular, it is not known whether all VSMCs proliferate and display plasticity or whether individual cells can switch to multiple phenotypes. OBJECTIVE: To assess whether proliferation and plasticity in disease is a general characteristic of VSMCs or a feature of a subset of cells. METHODS AND RESULTS: Using multicolor lineage labeling, we demonstrate that VSMCs in injury-induced neointimal lesions and in atherosclerotic plaques are oligoclonal, derived from few expanding cells. Lineage tracing also revealed that the progeny of individual VSMCs contributes to both alpha smooth muscle actin (aSma)-positive fibrous cap and Mac3-expressing macrophage-like plaque core cells. Costaining for phenotypic markers further identified a double-positive aSma+ Mac3+ cell population, which is specific to VSMC-derived plaque cells. In contrast, VSMC-derived cells generating the neointima after vascular injury generally retained the expression of VSMC markers and the upregulation of Mac3 was less pronounced. Monochromatic regions in atherosclerotic plaques and injury-induced neointima did not contain VSMC-derived cells expressing a different fluorescent reporter protein, suggesting that proliferation-independent VSMC migration does not make a major contribution to VSMC accumulation in vascular disease. CONCLUSIONS: We demonstrate that extensive proliferation of a low proportion of highly plastic VSMCs results in the observed VSMC accumulation after injury and in atherosclerotic plaques. Therapeutic targeting of these hyperproliferating VSMCs might effectively reduce vascular disease without affecting vascular integrity.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
siha发布了新的文献求助10
刚刚
ZE发布了新的文献求助10
刚刚
内向晓旋发布了新的文献求助10
刚刚
刚刚
嘞嘞发布了新的文献求助10
1秒前
www完成签到,获得积分10
1秒前
秋风的应助被黄梓同采纳,获得30
2秒前
2秒前
xht发布了新的文献求助10
2秒前
韶芸遥发布了新的文献求助10
2秒前
yzb完成签到,获得积分10
2秒前
3秒前
毛毛发布了新的文献求助10
4秒前
4秒前
123完成签到 ,获得积分20
4秒前
4秒前
4秒前
5秒前
5秒前
YiRan完成签到,获得积分10
5秒前
5秒前
zmy发布了新的文献求助10
5秒前
好运连连完成签到,获得积分10
6秒前
Niceeeee完成签到 ,获得积分20
6秒前
6秒前
7秒前
PORSCHE的FANS完成签到,获得积分10
7秒前
7秒前
大个的应助被内向晓旋采纳,获得10
7秒前
852的应助被科研通管家采纳,获得100
7秒前
李健的应助被科研通管家采纳,获得10
7秒前
sagitar的应助被科研通管家采纳,获得60
7秒前
汉堡包的应助被科研通管家采纳,获得10
7秒前
情怀的应助被科研通管家采纳,获得10
8秒前
zwkk的应助被科研通管家采纳,获得10
8秒前
szyd发布了新的文献求助10
8秒前
阿波卡利斯完成签到,获得积分10
8秒前
希望天下0贩的0的应助被komorebi采纳,获得10
8秒前
毛毛发布了新的文献求助10
8秒前
xiduoduo发布了新的文献求助30
9秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Encyclopedia of Modern Artificial Intelligence 1000
Особенности технологий и методов информационно-психологических войн СССР с Великобританией и США в период 1939-1953 гг 1000
Das Matthäusevangelium: Kapitel 1:1–17 1000
IRTSD: Open-Source Data and Toolset for Electromagnetic Transient Analysis of Disturbances and IBR Control Malfunctions in Transmission Systems 1000
Challenging Attachment Theory 600
Analyses de reconnaissances de dettes passées devant les échevins d'Ypres (1249-1291) 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8139865
求助须知:如何正确求助?哪些是违规求助? 9540304
关于积分的说明 21638716
捐赠科研通 7723987
什么是DOI,文献DOI怎么找? 3420921
关于科研通互助平台的介绍 2546124
邀请新用户注册赠送积分活动 2462905