清晨好,您是今天最早来到科研通的研友!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您科研之路漫漫前行!

Identification of Epigenetic Regulators of Vascular Calcification with a CRISPR-Based Screen.

清脆的 鉴定(生物学) 表观遗传学 钙化 计算生物学 生物 医学 遗传学 内科学 基因 生态学
作者
Yaxin Lian,Chen Xie,M Feng,Huijin Zhu,Xin Chen,Xiaolin Liu,Yun Cheung Kong,Dajiang He,Jianshuai Ma,Yuxi Chen,H. Zhang,Aoran Huang,Yanlian Chen,Hui Huang
出处
期刊:PubMed
标识
DOI:10.1681/asn.0000000793
摘要

Vascular calcification, mainly driven by osteogenic transdifferentiation of vascular smooth muscle cells (VSMCs), is a common pathological condition in patients with chronic kidney disease. However, the roles of other epigenetic regulators in this process remain largely unexplored. CRISPR screen is a highly efficient strategy widely used in identifying genes related to various biological processes. However, the lack of suitable cell sorting strategies combined with CRISPR screen meant this technology had not been applied to gene screening in vascular calcification. We performed an epigenetic-focused CRISPR screen in primary human VSMCs and identified key genes and pathways underlying osteogenic transdifferentiation, based on sgRNA enrichment in RANKL + (calcified) and RANKL - (noncalcified) VSMCs isolated by magnetic activated cell sorting. To validate the screen results, potential genes with different rankings were validated by siRNA intervention and Alizarin Red S staining. Integrating CRISPR results with transcriptome data revealed 17 critical regulators. We further investigated the top hit, Anthrax Toxin Receptor 1 (ANTXR1), in vascular calcification by examining clinical human samples and intervention in mice model. Through CRISPR screen, we identified 122 potential genes positive-regulating vascular calcification and 116 negative-regulating genes. Phenotypic experimental results further verified the roles of genes with different rankings in osteogenic transdifferentiation of VSMCs, reinforcing the validity of our CRISPR screen system. Notably, integrative analysis of CRISPR screen with transcriptome data revealed ANTXR1 as a critical factor regulating vascular calcification. Furthermore, detection of clinical human samples confirmed the upregulation of ANTXR1 during calcification. Knockdown of ANTXR1 suppressed vascular calcification in mice model; likewise, overexpression promoted vascular calcification and the osteogenic transdifferentiation of VSMCs. Our epigenetic-focused CRISPR screen and transcriptome analysis identified critical epigenetic genes involved in vascular calcification.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
和谐的夏岚完成签到 ,获得积分0
10秒前
shlw完成签到,获得积分10
14秒前
18秒前
哈哈完成签到 ,获得积分10
20秒前
彩色的芷容完成签到 ,获得积分10
25秒前
糖诗完成签到 ,获得积分10
33秒前
glomming完成签到 ,获得积分10
34秒前
卫卫完成签到 ,获得积分10
35秒前
32429606完成签到 ,获得积分10
38秒前
宝贝完成签到 ,获得积分10
38秒前
点点完成签到 ,获得积分10
40秒前
44秒前
早日发文章完成签到,获得积分10
45秒前
46秒前
xiaowuge完成签到 ,获得积分10
49秒前
Mine发布了新的文献求助10
50秒前
nav完成签到 ,获得积分10
52秒前
guhao完成签到 ,获得积分10
53秒前
科目三应助Mine采纳,获得10
58秒前
ZGH完成签到,获得积分10
1分钟前
zhang完成签到 ,获得积分10
1分钟前
1分钟前
喝酸奶不舔盖完成签到 ,获得积分10
1分钟前
霸气秀完成签到 ,获得积分10
1分钟前
tingting完成签到 ,获得积分10
1分钟前
1分钟前
红枫没有微雨怜完成签到 ,获得积分10
1分钟前
丝丢皮的完成签到 ,获得积分10
1分钟前
1分钟前
量子星尘发布了新的文献求助20
1分钟前
领导范儿应助123采纳,获得10
1分钟前
橙汁摇一摇完成签到 ,获得积分10
1分钟前
活力的妙之完成签到 ,获得积分10
1分钟前
木野狐完成签到,获得积分10
1分钟前
1分钟前
求知小生完成签到 ,获得积分10
1分钟前
苗笑卉发布了新的文献求助10
1分钟前
HY完成签到 ,获得积分10
1分钟前
猪仔5号完成签到 ,获得积分10
1分钟前
su完成签到 ,获得积分0
1分钟前
高分求助中
Semantics for Latin: An Introduction 1155
Genomic signature of non-random mating in human complex traits 1000
Plutonium Handbook 1000
Three plays : drama 1000
Robot-supported joining of reinforcement textiles with one-sided sewing heads 600
SPSS for Windows Step by Step: A Simple Study Guide and Reference, 17.0 Update (10th Edition) 500
Multimodal injustices: Speech acts, gender bias, and speaker’s status 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4105955
求助须知:如何正确求助?哪些是违规求助? 3643901
关于积分的说明 11542799
捐赠科研通 3350948
什么是DOI,文献DOI怎么找? 1841188
邀请新用户注册赠送积分活动 907911
科研通“疑难数据库(出版商)”最低求助积分说明 825065