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富含原纤维蛋白的微原纤维:正常人晶状体悬韧带衰老过程中的结构改变

Fibrillin-rich microfibrils: structural modifications during ageing in normal human zonule.

作者信息

Hanssen E, Franc S, Garrone R

机构信息

Institute of Biology and Chemistry of Proteins, CNRS UPR 412, Lyon, France.

出版信息

J Submicrosc Cytol Pathol. 1998 Jul;30(3):365-9.

PMID:9723196
Abstract

Ageing is marked by ultrastructural and functional changes in most tissues. In part, these changes are caused by a loss of elasticity in the elastic fibers of the extracellular matrix. These fibers are composed of the protein elastin associated with microfibrils of 8 to 12 nm in diameter. Microfibrils contain fibrillins as major constituents. Mutations in fibrillin genes are considered as primary causes of Marfan syndrome, a genetic disorder with pathological manifestations in the cardiovascular and skeletal systems, in addition to dysfunctions in the eye. Fibrillin is also the major protein of the ciliary zonule fibers. During ageing, these fibers become more fragile, and concomitantly, an increased risk for ocular pathologies is observed. We have investigated structural modifications in fibrillin-rich microfibrils during ageing of human ciliary zonule. Observations using light microscopy and transmission electron microscopy after rotary shadowing allowed us to describe the organization of the zonule fibers and their insertion into the ciliary body. Our results emphasize qualitative differences between young and old zonules, which are likely due to modifications in the structure of microfibrils.

摘要

衰老的特征是大多数组织发生超微结构和功能变化。部分这些变化是由细胞外基质弹性纤维弹性丧失引起的。这些纤维由与直径为8至12纳米的微原纤维相关的弹性蛋白组成。微原纤维以原纤蛋白作为主要成分。原纤蛋白基因的突变被认为是马凡综合征的主要病因,马凡综合征是一种遗传性疾病,除了眼部功能障碍外,还在心血管和骨骼系统出现病理表现。原纤蛋白也是睫状小带纤维的主要蛋白质。在衰老过程中,这些纤维变得更加脆弱,同时观察到眼部病变风险增加。我们研究了人睫状小带衰老过程中富含原纤蛋白的微原纤维的结构变化。使用旋转阴影后的光学显微镜和透射电子显微镜观察使我们能够描述小带纤维的组织及其插入睫状体的情况。我们的结果强调了年轻和年老小带之间的质的差异,这可能是由于微原纤维结构的改变所致。

相似文献

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Fibrillin microfibrils.原纤维微原纤维
Adv Protein Chem. 2005;70:405-36. doi: 10.1016/S0065-3233(05)70012-7.

引用本文的文献

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Fibrillin and the eye.原纤维蛋白与眼睛。
Br J Ophthalmol. 2000 Nov;84(11):1312-7. doi: 10.1136/bjo.84.11.1312.

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