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Periostin regulates collagen fibrillogenesis and the biomechanical properties of connective tissues.

机译:骨膜素调节胶原纤维原纤维形成和结缔组织的生物力学特性。

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摘要

Periostin is predominantly expressed in collagen-rich fibrous connective tissues that are subjected to constant mechanical stresses including: heart valves, tendons, perichondrium, cornea, and the periodontal ligament (PDL). Based on these data we hypothesize that periostin can regulate collagen I fibrillogenesis and thereby affect the biomechanical properties of connective tissues. Immunoprecipitation and immunogold transmission electron microscopy experiments demonstrate that periostin is capable of directly interacting with collagen I. To analyze the potential role of periostin in collagen I fibrillogenesis, gene targeted mice were generated. Transmission electron microscopy and morphometric analyses demonstrated reduced collagen fibril diameters in skin dermis of periostin knockout mice, an indication of aberrant collagen I fibrillogenesis. In addition, differential scanning calorimetry (DSC) demonstrated a lower collagen denaturing temperature in periostin knockout mice, reflecting a reduced levelof collagen cross-linking. Functional biomechanical properties of periostin null skin specimens and atrioventricular (AV) valve explant experiments provided direct evidence of the role that periostin plays in regulating the viscoelastic properties of connective tissues. Collectively, these data demonstrate for the first time that periostin can regulate collagen I fibrillogenesis and thereby serves as an important mediator of the biomechanical properties of fibrous connective tissues.
机译:骨膜素主要在经受持续机械应力的富含胶原蛋白的纤维结缔组织中表达,包括:心脏瓣膜,肌腱,软骨膜,角膜和牙周膜(PDL)。基于这些数据,我们假设骨膜素可以调节I型胶原的原纤维形成,从而影响结缔组织的生物力学特性。免疫沉淀和免疫金透射电子显微镜实验表明,骨膜素能够直接与胶原蛋白I相互作用。为了分析骨膜素在胶原蛋白I原纤维形成中的潜在作用,生成了基因靶向小鼠。透射电子显微镜和形态分析表明,骨膜素敲除小鼠的皮肤真皮中的胶原原纤维直径降低,这表明胶原I原纤维形成异常。此外,差示扫描量热法(DSC)证明了骨膜素敲除小鼠的胶原变性温度较低,反映了胶原交联水平降低。骨膜素无效皮肤样本的功能生物力学特性和房室(AV)瓣膜外植体实验提供了骨膜素在调节结缔组织粘弹性中所起作用的直接证据。总的来说,这些数据首次证明了骨膜素可以调节胶原蛋白I的原纤维形成,从而成为纤维结缔组织生物力学特性的重要介质。

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