CCN proteins: multifunctional signalling regulators

CTGF公司 肝星状细胞 细胞生物学 日历年61 生长因子 基因亚型 细胞粘附 血管生成 生物 化学 细胞 受体 癌症研究 遗传学 内分泌学 基因
作者
Bernard Perbal
出处
期刊:The Lancet [Elsevier]
卷期号:363 (9402): 62-64 被引量:706
标识
DOI:10.1016/s0140-6736(03)15172-0
摘要

Although little is known as yet about the processes that coordinate cell-signalling pathways, matrix proteins are probably major players in this type of global control. The CCN (cyr61, ctgf, nov) proteins are an important family of matricellular regulatory factors involved in internal and external cell signalling. This family participates in angiogenesis, chondrogenesis, and osteogenesis, and they are probably involved in the control of cell proliferation and differentiation.Runping Gao and David Brigstock (Hepatol Res 2003; 27: 214-20) recently showed that CCN2 (CTGF, connective tissue growth factor) is a cell-adhesion factor for hepatic stellate cells. On exposure to transforming growth factor beta, hepatic stellate cells produce distinct CCN2 isoforms. Gao and Brigstock assign to CCN2 module 3 the capacity to mediate binding to low-density-lipoprotein receptor-related protein (LRP), which was previously reported to interact with CCN2 and to be involved in various types of signalling. They also establish that CCN2 binding to LRP is heparin dependent and that module 4 of CCN2 promotes LRP-independent adhesion of hepatic stellate cells. The differential binding of CCN2 isoforms to LRP highlights the importance of functional interactions between individual modules, and reinforces the concept that different module combinations might confer agonistic or antagonistic activities. WHERE NEXT? It is essential to understand how the distinct configuration of the various CCN isoform affects their biological activities and bioavailability, and to explore the mechanisms and the regulatory processes involved in the production of truncated CCN isoforms. A better understanding of the structural basis for their multifunctionality is a prerequisite to wider use of CCN proteins in molecular medicine.
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
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
周老师完成签到 ,获得积分10
1秒前
顾矜应助下笔如有神采纳,获得10
1秒前
小猪完成签到,获得积分10
1秒前
张雨茜发布了新的文献求助30
1秒前
小马甲应助niruicheng采纳,获得10
2秒前
高文强发布了新的文献求助10
2秒前
3秒前
平常平凡发布了新的文献求助10
3秒前
帅气的宽完成签到 ,获得积分10
7秒前
随遇而安应助MM采纳,获得20
8秒前
培a发布了新的文献求助10
8秒前
脑洞疼应助lz采纳,获得50
8秒前
清晨的小鹿完成签到,获得积分10
9秒前
糟糕的绮露完成签到,获得积分10
9秒前
dyk发布了新的文献求助10
9秒前
刘芬完成签到,获得积分10
10秒前
思源应助科研鼠采纳,获得10
10秒前
11秒前
子非我发布了新的文献求助10
11秒前
Meyako应助踏实的蘑菇采纳,获得20
11秒前
songyu完成签到,获得积分10
11秒前
jin发布了新的文献求助10
12秒前
12秒前
12秒前
13秒前
wp完成签到,获得积分10
13秒前
今后应助平常平凡采纳,获得10
13秒前
旅客完成签到,获得积分10
14秒前
zl12345完成签到,获得积分10
14秒前
培a完成签到,获得积分10
14秒前
ZDD发布了新的文献求助10
15秒前
行健灵山完成签到 ,获得积分10
15秒前
困困包应助叶子采纳,获得10
16秒前
16秒前
16秒前
gt完成签到,获得积分10
16秒前
diu举报Alex求助涉嫌违规
16秒前
嘿嘿发布了新的文献求助10
16秒前
高文强完成签到,获得积分10
16秒前
张雨茜完成签到,获得积分10
16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
HIGH DYNAMIC RANGE CMOS IMAGE SENSORS FOR LOW LIGHT APPLICATIONS 1500
Bandwidth Choice for Bias Estimators in Dynamic Nonlinear Panel Models 1000
Constitutional and Administrative Law 1000
The Social Work Ethics Casebook: Cases and Commentary (revised 2nd ed.). Frederic G. Reamer 800
Holistic Discourse Analysis 600
Vertébrés continentaux du Crétacé supérieur de Provence (Sud-Est de la France) 600
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 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5354035
求助须知:如何正确求助?哪些是违规求助? 4486507
关于积分的说明 13966675
捐赠科研通 4386923
什么是DOI,文献DOI怎么找? 2410096
邀请新用户注册赠送积分活动 1402435
关于科研通互助平台的介绍 1376249