Suppr超能文献

层粘连蛋白-211 在骨骼肌功能中的作用。

Laminin-211 in skeletal muscle function.

机构信息

Muscle Biology Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.

出版信息

Cell Adh Migr. 2013 Jan-Feb;7(1):111-21. doi: 10.4161/cam.22618. Epub 2012 Nov 15.

Abstract

A chain is no stronger than its weakest link is an old idiom that holds true for muscle biology. As the name implies, skeletal muscle's main function is to move the bones. However, for a muscle to transmit force and withstand the stress that contractions give rise to, it relies on a chain of proteins attaching the cytoskeleton of the muscle fiber to the surrounding extracellular matrix. The importance of this attachment is illustrated by a large number of muscular dystrophies caused by interruption of the cytoskeletal-extracellular matrix interaction. One of the major components of the extracellular matrix is laminin, a heterotrimeric glycoprotein and a major constituent of the basement membrane. It has become increasingly apparent that laminins are involved in a multitude of biological functions, including cell adhesion, differentiation, proliferation, migration and survival. This review will focus on the importance of laminin-211 for normal skeletal muscle function.

摘要

“链条的强度取决于其最薄弱的环节”是一句古老的谚语,它在肌肉生物学中同样适用。顾名思义,骨骼肌的主要功能是移动骨骼。然而,为了使肌肉能够传递力量并承受收缩产生的应力,它依赖于一系列将肌纤维的细胞骨架连接到周围细胞外基质的蛋白质。这种连接的重要性可以通过大量由细胞骨架-细胞外基质相互作用中断引起的肌肉营养不良症来说明。细胞外基质的主要成分之一是层粘连蛋白,它是一种异三聚体糖蛋白,也是基底膜的主要成分。越来越明显的是,层粘连蛋白参与了多种生物学功能,包括细胞黏附、分化、增殖、迁移和存活。这篇综述将重点介绍层粘连蛋白-211 对正常骨骼肌功能的重要性。

相似文献

1
Laminin-211 in skeletal muscle function.
Cell Adh Migr. 2013 Jan-Feb;7(1):111-21. doi: 10.4161/cam.22618. Epub 2012 Nov 15.
2
Laminins during muscle development and in muscular dystrophies.
Cell Mol Life Sci. 1999 Oct 30;56(5-6):442-60. doi: 10.1007/pl00000616.
3
Extracellular matrix-driven congenital muscular dystrophies.
Matrix Biol. 2018 Oct;71-72:188-204. doi: 10.1016/j.matbio.2018.06.005. Epub 2018 Jun 19.
4
Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.
Hum Mol Genet. 2012 Nov 1;21(21):4718-31. doi: 10.1093/hmg/dds312. Epub 2012 Jul 31.
8
Cell adhesion in muscle.
Braz J Med Biol Res. 1994 Sep;27(9):2213-27.
9
The myotomal basement membrane: insight into laminin-111 function and its control by Sonic hedgehog signaling.
Cell Adh Migr. 2013 Jan-Feb;7(1):72-81. doi: 10.4161/cam.23411. Epub 2013 Jan 1.

引用本文的文献

1
Broadening the paradigm of laminin α2-related muscular dystrophy: A case of partial merosin deficiency with compound heterozygous variants.
SAGE Open Med Case Rep. 2025 Aug 25;13:2050313X251366020. doi: 10.1177/2050313X251366020. eCollection 2025.
2
Force-dependent development of the myodural bridge in rats: The impact of Integrin α7.
PLoS One. 2025 Aug 4;20(8):e0329754. doi: 10.1371/journal.pone.0329754. eCollection 2025.
5
Hidden pathway: the role of extracellular matrix in type 2 diabetes mellitus-related sarcopenia.
Front Endocrinol (Lausanne). 2025 Apr 16;16:1560396. doi: 10.3389/fendo.2025.1560396. eCollection 2025.
10
Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches.
Dis Model Mech. 2024 Oct 1;17(10). doi: 10.1242/dmm.050720. Epub 2024 Nov 6.

本文引用的文献

2
Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE.
Science. 2012 Jan 6;335(6064):93-6. doi: 10.1126/science.1214115.
3
β1D chain increases α7β1 integrin and laminin and protects against sarcolemmal damage in mdx mice.
Hum Mol Genet. 2012 Apr 1;21(7):1592-603. doi: 10.1093/hmg/ddr596. Epub 2011 Dec 16.
4
Cell-matrix interactions in muscle disease.
J Pathol. 2012 Jan;226(2):200-18. doi: 10.1002/path.3020.
6
Forced expression of laminin beta1 in podocytes prevents nephrotic syndrome in mice lacking laminin beta2, a model for Pierson syndrome.
Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15348-53. doi: 10.1073/pnas.1108269108. Epub 2011 Aug 29.
7
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.
Skelet Muscle. 2011 Mar 1;1(1):9. doi: 10.1186/2044-5040-1-9.
8
Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice.
EMBO Mol Med. 2011 Aug;3(8):465-79. doi: 10.1002/emmm.201100151. Epub 2011 Jun 15.
9
COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans.
PLoS Genet. 2011 May;7(5):e1002062. doi: 10.1371/journal.pgen.1002062. Epub 2011 May 19.

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