Mechanotransduction and epigenetic modulations of chromatin: Role of mechanical signals in gene regulation

机械转化 染色质 细胞骨架 信号转导 细胞生物学 机械敏感通道 转录因子 生物 基因 化学 遗传学 细胞 离子通道 受体
作者
Jagdish Mishra,Subhajit Chakraborty,Niharika Niharika,Ankan Roy,Soumen K. Manna,Tirthankar Baral,Piyasa Nandi,Samir Kumar Patra
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:125 (3): e30531-e30531 被引量:22
标识
DOI:10.1002/jcb.30531
摘要

Mechanical forces may be generated within a cell due to tissue stiffness, cytoskeletal reorganization, and the changes (even subtle) in the cell's physical surroundings. These changes of forces impose a mechanical tension within the intracellular protein network (both cytosolic and nuclear). Mechanical tension could be released by a series of protein-protein interactions often facilitated by membrane lipids, lectins and sugar molecules and thus generate a type of signal to drive cellular processes, including cell differentiation, polarity, growth, adhesion, movement, and survival. Recent experimental data have accentuated the molecular mechanism of this mechanical signal transduction pathway, dubbed mechanotransduction. Mechanosensitive proteins in the cell's plasma membrane discern the physical forces and channel the information to the cell interior. Cells respond to the message by altering their cytoskeletal arrangement and directly transmitting the signal to the nucleus through the connection of the cytoskeleton and nucleoskeleton before the information despatched to the nucleus by biochemical signaling pathways. Nuclear transmission of the force leads to the activation of chromatin modifiers and modulation of the epigenetic landscape, inducing chromatin reorganization and gene expression regulation; by the time chemical messengers (transcription factors) arrive into the nucleus. While significant research has been done on the role of mechanotransduction in tumor development and cancer progression/metastasis, the mechanistic basis of force-activated carcinogenesis is still enigmatic. Here, in this review, we have discussed the various cues and molecular connections to better comprehend the cellular mechanotransduction pathway, and we also explored the detailed role of some of the multiple players (proteins and macromolecular complexes) involved in mechanotransduction. Thus, we have described an avenue: how mechanical stress directs the epigenetic modifiers to modulate the epigenome of the cells and how aberrant stress leads to the cancer phenotype.
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
科研通AI6.4应助SSNN采纳,获得30
刚刚
冷静玫瑰发布了新的文献求助30
刚刚
科研通AI6.4应助雪雪采纳,获得10
1秒前
1秒前
wave完成签到,获得积分10
1秒前
2秒前
wangjing11完成签到,获得积分10
3秒前
希望天下0贩的0应助妮儿采纳,获得10
4秒前
常淼淼发布了新的文献求助10
5秒前
6秒前
无咎0623完成签到 ,获得积分10
7秒前
轻松的冥王星完成签到,获得积分10
7秒前
CodeCraft应助落后的忆南采纳,获得10
8秒前
余追发布了新的文献求助30
8秒前
9秒前
wenjing发布了新的文献求助10
9秒前
12秒前
12秒前
懵懂的枫叶完成签到,获得积分10
12秒前
搜集达人应助未步采纳,获得10
12秒前
爱喷火的小恐龙完成签到,获得积分20
12秒前
高国豪完成签到 ,获得积分10
14秒前
mayaxi发布了新的文献求助20
15秒前
16秒前
17秒前
xifala完成签到,获得积分10
18秒前
20秒前
李白发布了新的文献求助10
20秒前
YY完成签到 ,获得积分10
20秒前
爱喷火的小恐龙关注了科研通微信公众号
20秒前
18863933521发布了新的文献求助10
20秒前
22秒前
拾英完成签到,获得积分10
22秒前
22秒前
Cc完成签到,获得积分10
23秒前
科研通AI6.4应助SSNN采纳,获得10
23秒前
FashionBoy应助alano采纳,获得10
23秒前
24秒前
25秒前
ZRT134发布了新的文献求助10
25秒前
高分求助中
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
Understanding Modeling and Simulation of Polymerization Reactions 400
Direct and Iterative Linear System Solvers 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6901480
求助须知:如何正确求助?哪些是违规求助? 8596048
关于积分的说明 18249628
捐赠科研通 6302136
什么是DOI,文献DOI怎么找? 3062456
关于科研通互助平台的介绍 2083642
邀请新用户注册赠送积分活动 2040378