Suppr超能文献

在心脏发育和重构中特别有趣的半胱氨酸和组氨酸丰富蛋白。

Particularly interesting cysteine- and histidine-rich protein in cardiac development and remodeling.

机构信息

Department of Medicine, University of California at San Diego (UCSD), La Jolla, CA 92093-0613C, USA.

出版信息

J Investig Med. 2009 Dec;57(8):842-8. doi: 10.2310/JIM.0b013e3181c5e31d.

Abstract

Integrin-mediated cell-extracellular matrix interaction plays key roles in tissue morphogenesis and integrity. The Lin11-Isl-1-Mec-3 (LIM) domain-only particularly interesting cysteine- and histidine-rich (PINCH) protein functions as an adaptor essential for the assembly and function of the focal adhesion complex that links integrin signaling to the cytoskeleton and other intracellular signaling pathways and regulates diverse cellular processes such as cell adhesion, migration, growth, differentiation, and survival. Recent biochemical and genetic studies have greatly advanced our knowledge surrounding the molecular interactions and functions of each component of the focal adhesion complex and revealed a requirement for PINCH in early embryogenesis, in morphogenesis of the neural crest and cardiac outflow, and in myocardial growth and remodeling. In this review article, we will provide an overview of the current knowledge of the molecular interactions of PINCH with other components of focal adhesions, highlighting recent discoveries of the in vivo role of PINCH and discuss its potential implication for human heart disease.

摘要

整合素介导的细胞-细胞外基质相互作用在组织形态发生和完整性中发挥着关键作用。Lin11-Isl-1-Mec-3(LIM)结构域仅有特别有趣的半胱氨酸和组氨酸丰富(PINCH)蛋白作为衔接蛋白,对于整合素信号与细胞骨架和其他细胞内信号通路的连接的粘着斑复合物的组装和功能是必不可少的,并且调节各种细胞过程,如细胞黏附、迁移、生长、分化和存活。最近的生化和遗传研究极大地提高了我们对粘着斑复合物每个成分的分子相互作用和功能的认识,并揭示了 PINCH 在早期胚胎发生、神经嵴和心脏流出道形态发生以及心肌生长和重塑中的重要作用。在这篇综述文章中,我们将概述 PINCH 与粘着斑其他成分的分子相互作用的最新知识,重点介绍 PINCH 的体内作用的最新发现,并讨论其对人类心脏病的潜在意义。

相似文献

1
Particularly interesting cysteine- and histidine-rich protein in cardiac development and remodeling.
J Investig Med. 2009 Dec;57(8):842-8. doi: 10.2310/JIM.0b013e3181c5e31d.
2
Structural basis of focal adhesion localization of LIM-only adaptor PINCH by integrin-linked kinase.
J Biol Chem. 2009 Feb 27;284(9):5836-44. doi: 10.1074/jbc.M805319200. Epub 2008 Dec 30.
4
Signaling via PINCH: Functions, binding partners and implications in human diseases.
Gene. 2016 Dec 5;594(1):10-15. doi: 10.1016/j.gene.2016.08.039. Epub 2016 Aug 30.
7
Structural and functional insights into PINCH LIM4 domain-mediated integrin signaling.
Nat Struct Biol. 2003 Jul;10(7):558-64. doi: 10.1038/nsb938.
8
Signalling via integrins: implications for cell survival and anticancer strategies.
Biochim Biophys Acta. 2007 Jan;1775(1):163-80. doi: 10.1016/j.bbcan.2006.09.001. Epub 2006 Oct 4.
9
PINCH, N(i)ck and the ILK: network wiring at cell-matrix adhesions.
Trends Cell Biol. 2005 Sep;15(9):460-6. doi: 10.1016/j.tcb.2005.07.002.
10
Significance of thymosin β4 and implication of PINCH-1-ILK-α-parvin (PIP) complex in human dilated cardiomyopathy.
PLoS One. 2011;6(5):e20184. doi: 10.1371/journal.pone.0020184. Epub 2011 May 19.

引用本文的文献

1
Osteocytic vinculin controls bone mass by modulating Mef2c-driven sclerostin expression in mice.
Bone Res. 2025 Aug 13;13(1):73. doi: 10.1038/s41413-025-00452-x.
2
Cysteine Redox Chemistry in Peptide Self-Assembly to Modulate Hydrogelation.
Molecules. 2023 Jun 24;28(13):4970. doi: 10.3390/molecules28134970.
3
Requirement for PINCH in skeletal myoblast differentiation.
Cell Tissue Res. 2023 Jan;391(1):205-215. doi: 10.1007/s00441-022-03701-1. Epub 2022 Nov 17.
4
Understanding the molecular basis of cardiomyopathy.
Am J Physiol Heart Circ Physiol. 2022 Feb 1;322(2):H181-H233. doi: 10.1152/ajpheart.00562.2021. Epub 2021 Nov 19.
6
The costamere bridges sarcomeres to the sarcolemma in striated muscle.
Prog Pediatr Cardiol. 2011 May;31(2):83-88. doi: 10.1016/j.ppedcard.2011.02.003.

本文引用的文献

1
Targeted ablation of PINCH1 and PINCH2 from murine myocardium results in dilated cardiomyopathy and early postnatal lethality.
Circulation. 2009 Aug 18;120(7):568-76. doi: 10.1161/CIRCULATIONAHA.109.864686. Epub 2009 Aug 3.
2
Cardiac fibroblasts regulate myocardial proliferation through beta1 integrin signaling.
Dev Cell. 2009 Feb;16(2):233-44. doi: 10.1016/j.devcel.2008.12.007.
3
The Rsu-1-PINCH1-ILK complex is regulated by Ras activation in tumor cells.
Eur J Cell Biol. 2008 Sep;87(8-9):721-34. doi: 10.1016/j.ejcb.2008.02.011. Epub 2008 Apr 23.
4
Thymosin beta4 is cardioprotective after myocardial infarction.
Ann N Y Acad Sci. 2007 Sep;1112:161-70. doi: 10.1196/annals.1415.048. Epub 2007 Jun 28.
5
Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures.
Circ Res. 2007 Mar 2;100(4):527-35. doi: 10.1161/01.RES.0000259041.37059.8c. Epub 2007 Feb 1.
7
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695.
8
ILK, PINCH and parvin: the tIPP of integrin signalling.
Nat Rev Mol Cell Biol. 2006 Jan;7(1):20-31. doi: 10.1038/nrm1789.
9
Establishment of cardiac cytoarchitecture in the developing mouse heart.
Dev Biol. 2006 Jan 15;289(2):430-41. doi: 10.1016/j.ydbio.2005.10.046. Epub 2005 Dec 9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验