Matricellular proteins in the trabecular meshwork

被引:58
作者
Rhee, Douglas J. [1 ]
Haddadin, Ramez I. [1 ]
Kang, Min Hyung [1 ]
Oh, Dong-Jin [1 ]
机构
[1] Massachusetts Eye & Ear Infirm, Dept Ophthalmol, Boston, MA 02114 USA
关键词
trabecular meshwork; matricellular proteins; SPARC; thrombospondin; tenascin; osteopontin; hevin; galectin; extracellular matrix; GROWTH-FACTOR-BETA; SPARC-NULL MICE; EXTRACELLULAR-MATRIX PROTEINS; EHLERS-DANLOS-SYNDROME; THROMBIN-SENSITIVE PROTEIN; OSTEOPONTIN-DEFICIENT MICE; PIGMENT EPITHELIAL-CELLS; TENASCIN-X DEFICIENCY; CILIARY MUSCLE-CELLS; S-TYPE LECTIN;
D O I
10.1016/j.exer.2008.11.032
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The trabecular meshwork is one of the primary tissues of interest in the normal regulation and dysregulation of intraocular pressure (IOP) that is a causative risk factor for primary open-angle glaucoma. Matricellular proteins generally function to allow cells to modulate their attachments with and alter the characteristics of their surrounding extracellular matrix (ECM). In non-ocular tissues, matricellular proteins generally increase fibrosis. Since ECM turnover is very important to the outflow facility, matricellular proteins may have a significant role in the regulation of IOP. The formalized study of matricellular proteins in trabecular meshwork is in its infancy. SPARC, thrombospondins-1 and -2, and tenascins-C and -X, and osteopontin have been localized to varying areas within the trabecular meshwork. Preliminary evidence indicates that SPARC and thrombospondin-1 play a role in the regulation of IOP and possibly the pathophysiology of glaucoma. These data show promise that matricellular proteins are involved in IOP dysregulation and are potential therapeutic targets. Further study is needed to clarify these roles. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:694 / 703
页数:10
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