...
首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Depletion of annexin A5, annexin A6, and collagen X causes no gross changes in matrix vesicle-mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 response
【24h】

Depletion of annexin A5, annexin A6, and collagen X causes no gross changes in matrix vesicle-mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 response

机译:膜联蛋白A5,膜联蛋白A6和胶原蛋白X的消耗不会引起基质囊泡介导的矿化作用的明显改变,但是缺乏胶原蛋白X会影响造血作用和Th1 / Th2反应

获取原文
获取原文并翻译 | 示例

摘要

Numerous biochemical studies have pointed to an essential role of annexin A5 (AnxA5), annexin A6 (AnxA6), and collagen X in matrix vesicle-mediated biomineralization during endochondral ossification and in osteoarthritis. By binding to the extracellular matrix protein collagen X and matrix vesicles, annexins were proposed to anchor matrix vesicles in the extracellular space of hypertrophic chondrocytes to initiate the calcification of cartilage. However, mineralization appears to be normal in mice lacking AnxA5 and AnxA6, whereas collagen X-deficient mice show only subtle alterations in the growth plate organization. We hypothesized that the simultaneous lack of AnxA5, AnxA6, and collagen X in vivo induces more pronounced changes in the growth plate development and the initiation of mineralization. In this study, we generated and analyzed mice deficient for AnxA5, AnxA6, and collagen X. Surprisingly, mice were viable, fertile, and showed no obvious abnormalities. Assessment of growth plate development indicated that the hypertrophic zone was expanded in Col10a1 -/- and AnxA5 -/-AnxA6 -/-Col10a1 -/- newborns, whereas endochondral ossification and mineralization were not affected in 13-day- and 1-month-old mutants. In peripheral quantitative computed tomography, no changes in the degree of biomineralization were found in femora of 1-month- and 1-year-old mutants even though the diaphyseal circumference was reduced in Col10a1 -/- and AnxA5 -/-AnxA6 -/-Col10a1 -/- mice. The percentage of naive immature IgM +/IgM + B cells and peripheral T-helper cells were increased in Col10a1 -/- and AnxA5 -/-AnxA6 -/-Col10a1 -/- mutants, and activated splenic T cells isolated from Col10a1 -/- mice secreted elevated levels of IL-4 and GM-CSF. Hence, collagen X is needed for hematopoiesis during endochondral ossification and for the immune response, but the interaction of annexin A5, annexin A6, and collagen X is not essential for physiological calcification of growth plate cartilage. Therefore, annexins and collagen X may rather fulfill functions in growth plate cartilage not directly linked to the mineralization process.
机译:许多生化研究指出膜联蛋白A5(AnxA5),膜联蛋白A6(AnxA6)和胶原蛋白X在软骨内骨化和骨关节炎期间基质囊泡介导的生物矿化中起着至关重要的作用。通过结合细胞外基质蛋白胶原蛋白X和基质囊泡,膜联蛋白被提议将基质囊泡锚定在肥大软骨细胞的细胞外空间,以启动软骨钙化。但是,在缺少AnxA5和AnxA6的小鼠中矿化似乎是正常的,而缺乏胶原蛋白X的小鼠在生长板组织中仅表现出细微的变化。我们假设体内同时缺乏AnxA5,AnxA6和胶原蛋白X会在生长板的发育和矿化的起始中引起更明显的变化。在这项研究中,我们生成并分析了AnxA5,AnxA6和胶原X缺乏的小鼠。令人惊讶的是,小鼠是活的,可育的,并且没有显示出明显的异常。生长板发育的评估表明,Col10a1-/-和AnxA5-/-AnxA6-/-Col10a1-/-新生儿中的肥大区扩大了,而13天和1个月内软骨内骨化和矿化不受影响旧的突变体。在外周定量计算机断层扫描中,即使Col10a1-/-和AnxA5-/-AnxA6-/-的骨干周长减小,在1个月和1岁的突变体的股骨中也没有发现生物矿化程度的变化。 Col10a1-/-小鼠。在Col10a1-/-和AnxA5-/-AnxA6-/-Col10a1-/-突变体和从Col10a1-//中分离出的活化的脾T细胞中,未成熟的IgM + / IgM + B细胞和外周T辅助细胞的百分比增加-小鼠分泌升高水平的IL-4和GM-CSF。因此,在软骨内骨化过程中造血和免疫反应需要胶原蛋白X,但是膜联蛋白A5,膜联蛋白A6和胶原蛋白X的相互作用对于生长板软骨的生理钙化不是必需的。因此,膜联蛋白和胶原蛋白X可能在未直接与矿化过程相关的生长板软骨中发挥功能。

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号