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野生型和 Alport 小鼠晶状体囊在渗透膨胀过程中的力学反应。

Mechanical response of wild-type and Alport murine lens capsules during osmotic swelling.

机构信息

Department of Biomedical Engineering, University of Minnesota, 7-105 Nils Hasselmo Hall, 312 Church St. SE, Minneapolis, MN 55455, United States.

出版信息

Exp Eye Res. 2013 Aug;113:87-91. doi: 10.1016/j.exer.2013.05.008. Epub 2013 May 21.

Abstract

The mechanical support of basement membranes, such as the lens capsule, is believed to arise from one of their main constituents - collagen IV. The basement membranes of the lens, kidney, and ear normally contain two different types of collagen IV networks, referred to as the major and minor chain networks. In Alport syndrome, a mutation in one of the minor chain COL4 genes leads to the absence of the minor chain network, causing life-threatening disturbances. We hypothesized that the absence of the minor chain network increases basement membrane distensibility, as measured in wild-type (n = 25) and Alport syndrome (n = 21) mice using the lens capsule as a model. Osmotic swelling experiments revealed direction-dependent changes. As a reflection of lens capsule properties, Alport lenses strained significantly more than wild-type lenses in the anterior-posterior direction, i.e. along their thickness, but not in the equatorial direction (p = 0.03 and p = 0.08, respectively). This is consistent with clinical data: Alport patients develop conical protrusions on the anterior and posterior lenticular poles. There was no evidence of significant change in total amount of collagen between Alport and wild-type lenses (p = 0.6). The observed differences in distensibility could indicate that the major chain network alone cannot fully compensate for the absence of the more highly cross-linked minor chain network, which is believed to be stronger, more stable, and resistant to deformation. The addition of mechanical information on Alport syndrome to the currently available biological data provides a fuller picture into the progression of the disease.

摘要

基底膜的机械支撑,如晶状体囊,被认为来源于其主要成分之一——IV 型胶原。晶状体、肾脏和耳朵的基底膜通常包含两种不同类型的 IV 型胶原网络,分别称为主要链网络和次要链网络。在 Alport 综合征中,一个次要链 COL4 基因的突变导致次要链网络缺失,从而导致危及生命的紊乱。我们假设,缺失次要链网络会增加基底膜的可扩展性,这可以通过将晶状体囊作为模型,在野生型(n = 25)和 Alport 综合征(n = 21)小鼠中进行测量。渗透膨胀实验显示出方向依赖性的变化。作为晶状体囊特性的反映,Alport 晶状体在前-后方向(即沿着其厚度)的应变明显大于野生型晶状体,而在赤道方向则没有(p = 0.03 和 p = 0.08,分别)。这与临床数据一致:Alport 患者在前、后晶状体极上形成圆锥形突起。Alport 和野生型晶状体之间的胶原总量没有明显变化(p = 0.6)。可扩展性的差异表明,主要链网络本身无法完全补偿更交联的次要链网络的缺失,后者被认为更强、更稳定且不易变形。将 Alport 综合征的机械信息添加到现有的生物学数据中,可以更全面地了解疾病的进展。

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