The regulatory roles of small leucine-rich proteoglycans in extracellular matrix assembly

被引:298
作者
Chen, Shoujun [1 ]
Birk, David E. [1 ]
机构
[1] Univ S Florida, Morsani Coll Med, Dept Mol Pharmacol & Physiol, Tampa, FL 33612 USA
基金
美国国家卫生研究院;
关键词
cell-matrix interactions; collagen; development; extracellular matrix; fibrillogenesis; glycosaminoglycans; human congenital stromal corneal dystrophy; pathophysiology; proteoglycans; SLRP; COLLAGEN TYPE-I; KERATAN SULFATE PROTEOGLYCAN; STROMAL CORNEAL-DYSTROPHY; ATOMIC-FORCE MICROSCOPY; REPEAT PROTEIN FAMILY; CORE PROTEIN; DERMATAN SULFATE; DEFICIENT MICE; LUMICAN-DEFICIENT; DIFFERENTIAL EXPRESSION;
D O I
10.1111/febs.12136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Small leucine-rich proteoglycans (SLRPs) are involved in a variety of biological and pathological processes. This review focuses on their regulatory roles in matrix assembly. SLRPs have protein cores and hypervariable glycosylation with multivalent binding abilities. During development, differential interactions of SLRPs with other molecules result in tissue-specific spatial and temporal distributions. The changing expression patterns play a critical role in the regulation of tissue-specific matrix assembly and therefore tissue function. SLRPs play significant structural roles within extracellular matrices. In addition, they play regulatory roles in collagen fibril growth, fibril organization and extracellular matrix assembly. Moreover, they are involved in mediating cellmatrix interactions. Abnormal SLRP expression and/or structures result in dysfunctional extracellular matrices and pathophysiology. Altered expression of SLRPs has been found in many disease models, and structural deficiency also causes altered matrix assembly. SLRPs regulate assembly of the extracellular matrix, which defines the microenvironment, modulating both the extracellular matrix and cellular functions, with an impact on tissue function.
引用
收藏
页码:2120 / 2137
页数:18
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