角膜溃疡形成前基底膜溶解的机制。

Mechanism of basement membrane dissolution preceding corneal ulceration.

作者信息

Matsubara M, Zieske J D, Fini M E

机构信息

Eye Research Institute, Boston, Massachusetts.

出版信息

Invest Ophthalmol Vis Sci. 1991 Dec;32(13):3221-37.

DOI:
PMID:1660857
Abstract

In animal models for corneal ulceration, the degradation of extracellular matrix components of the stroma does not occur until after the basement membrane underlying the corneal epithelium has disappeared. Using a thermal-burn model, it was demonstrated that epithelial basement membrane is degraded actively by products of corneal cells in a process that does not require the participation of polymorphonuclear leukocytes. A new gelatinolytic metalloproteinase, preliminarily identified as the matrix metalloproteinase, MMP-9, is synthesized and secreted by corneal cells with a timing appropriate for a role in basement membrane degradation. During healing of ulcers, when new matrix is being deposited actively in the burned tissue, a second new gelatinase appears in the cornea, preliminarily identified as a stable activated form of the matrix metalloproteinase, MMP-2. The timing of expression suggests a role for this enzyme in appropriate deposition and remodeling of new matrix in the regenerating corneal tissue.

摘要

在角膜溃疡的动物模型中,直到角膜上皮下方的基底膜消失后,基质的细胞外基质成分才会发生降解。使用热烧伤模型表明,角膜细胞的产物在一个不需要多形核白细胞参与的过程中积极地降解上皮基底膜。一种新的明胶分解金属蛋白酶,初步鉴定为基质金属蛋白酶MMP - 9,由角膜细胞合成并分泌,其时间与在基底膜降解中发挥作用相适宜。在溃疡愈合过程中,当新的基质在烧伤组织中积极沉积时,角膜中出现了第二种新的明胶酶,初步鉴定为基质金属蛋白酶MMP - 2的稳定活化形式。表达的时间表明该酶在再生角膜组织中适当沉积和重塑新基质方面发挥作用。

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