Brown R A, Kayser M, McLaughlin B, Weiss J B
Institute of Orthopaedics (University College London), Royal National Orthopaedic Hospital Trust, Stanmore, Middlesex, United Kingdom.
Exp Cell Res. 1993 Sep;208(1):1-9. doi: 10.1006/excr.1993.1216.
The regulation of cartilage resorption is important both in cartilage pathophysiology and angiogenesis. Previous work has identified a link between calcification and activation of collagenolysis. The aim here was to test whether production of collagenase itself is also calcification-dependent, using a high-density growth plate chondrocyte culture model of calcification. Ultrastructural studies indicated that calcification occurred around large hypertrophic cells. There was no indication of phagocytosis of crystals even by cells lying next to mineral aggregates, although remodeling of the organic matrix by cell processes was evident. Release of collagenase activity increased dramatically between 24 and 48 h postcalcification, from low or undetectable basal levels. In contrast, gelatinase production was not calcification-dependent. Collagenase was released almost entirely in the latent form, being a consequence of increased protein synthesis rather than activation of existing enzyme. This linkage of calcification with latent collagenase production represents part of a coordinated remodeling of both collagenous and mineral components of the matrix which may also extend, in vivo, to the control of microvascular invasion and resorption.
软骨吸收的调节在软骨病理生理学和血管生成中都很重要。先前的研究已经确定了钙化与胶原溶解激活之间的联系。这里的目的是使用钙化的高密度生长板软骨细胞培养模型,测试胶原酶本身的产生是否也依赖于钙化。超微结构研究表明,钙化发生在大型肥大细胞周围。即使是紧邻矿物质聚集体的细胞,也没有吞噬晶体的迹象,尽管细胞突起对有机基质的重塑很明显。钙化后24至48小时之间,胶原酶活性的释放从低水平或不可检测的基础水平急剧增加。相比之下,明胶酶的产生不依赖于钙化。胶原酶几乎完全以潜伏形式释放,这是蛋白质合成增加的结果,而不是现有酶的激活。钙化与潜伏性胶原酶产生之间的这种联系代表了基质中胶原成分和矿物质成分协同重塑的一部分,这在体内可能也延伸至对微血管侵袭和吸收的控制。