Matrix proteins promote matrix vesicle mineralization

基质蛋白促进基质囊泡矿化

• 批准号: 7118682
• 负责人: Ann K Rosenthal
• 金额: $ 16.02万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-09-02 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7118682
• 关键词: animal tissue; arthritis; articular cartilage; calcification; calcium binding protein; calcium disorder; cell free system; collagen; extracellular matrix proteins; osteoarthritis; osteocalcin; osteonectin; osteopontin; pathologic process; proteoglycan; vesicle /vacuole

DESCRIPTION (provided by applicant): Pathogenic calcium crystals, including calcium pyrophosphate (CPPD) and basic calcium phosphate (BCP) crystals are common components of osteoarthritic joints. These crystals identify a subset of patients with unusually severe, rapidly progressive, arthritis. Yet, how crystals form in the normally unmineralized articular cartilage matrix remains unknown. Matrix vesicles are membrane-bound, chondrocyte-derived, extracellular organelles implicated in calcium crystal formation. Preliminary findings strongly suggest that the surrounding extracelllular matrix in cartilage clearly influences the matrix vesicle's ability to mineralize. There is ample precedence for an important interaction between matrix vesicles and their surrounding extracellular environment in growth plate cartilage. While dramatic changes in articular cartilage matrix occur in both osteoarthritis and with calcium crystal deposition, little is known about the interaction of extracellular matrix and matrix vesicles in articular cartilage. We hypothesize that interactions between matrix vesicles and extracellular matrix components strongly influence the ability of articular cartilage matrix vesicles to generate pathologic calcium crystals. In this proposal, we will will use porcine articular cartilage matrix vesicles in a gel-based calcification model to study I) the effects of type II collagen on articular cartilage matrix vesicle mineralization, II) the effects of large and small proteoglycans on articular cartilage matrix vesicle mineralization, and IN) the effects of the calcium binding proteins (osteopontin, SPARC, and matrix gla protein) on articular cartilage matrix vesicle mineralization. The ultimate goal of this work is to understand the pathogenesis of calcium crystal formation in articular cartilage, so that specific therapies for this disabling disease can be designed.

描述（由申请人提供）：病原钙晶体，包括焦磷酸钙（CPPD）和碱性磷酸钙（BCP）晶体是骨关节关节的常见成分。这些晶体鉴定了一部分患有异常严重，快速进行性关节炎的患者。然而，通常未知的关节软骨基质中的晶体如何形成仍然未知。基质囊泡是膜结合的，软骨细胞衍生的，涉及钙晶体形成的细胞外细胞器。初步发现强烈表明，软骨中周围的细胞外基质显然会影响基质囊泡矿化的能力。在生长板软骨中，基质囊泡及其周围的细胞外环境之间存在重要的优势。虽然关节软骨基质的急剧变化在骨关节炎和钙晶体沉积中都发生，但对于关节软骨中细胞外基质和基质囊泡的相互作用知之甚少。我们假设基质囊泡与细胞外基质成分之间的相互作用强烈影响关节软骨基质囊泡产生病理钙晶体的能力。 In this proposal, we will will use porcine articular cartilage matrix vesicles in a gel-based calcification model to study I) the effects of type II collagen on articular cartilage matrix vesicle mineralization, II) the effects of large and small proteoglycans on articular cartilage matrix vesicle mineralization, and IN) the effects of the calcium binding proteins (osteopontin, SPARC,关节软骨基质囊泡矿化上的基质gla蛋白）。 这项工作的最终目的是了解关节软骨中钙晶体形成的发病机理，以便可以设计这种残疾疾病的特定疗法。