Birk D E, Trelstad R L
J Cell Biol. 1986 Jul;103(1):231-40. doi: 10.1083/jcb.103.1.231.
The formation of collagen fibrils, fibril bundles, and tissue-specific collagen macroaggregates by chick embryo tendon fibroblasts was studied using conventional and high voltage electron microscopy. During chick tendon morphogenesis, there are at least three extracellular compartments responsible for three levels of matrix organization: collagen fibrils, bundles, and collagen macroaggregates. Our observations indicate that the initial extracellular events in collagen fibrillogenesis occur within narrow cytoplasmic recesses, presumably under close cellular regulation. Collagen fibrils are formed within these deep, narrow recesses, which are continuous with the extracellular space. Where these narrow recesses fuse with the cell surface, it becomes highly convoluted with folds and processes that envelope forming fibril bundles. The bundles laterally associate and coalesce, forming aggregates within a third cell-defined extracellular compartment. Our interpretation is that this third compartment forms as cell processes retract and cytoplasm is withdrawn between bundles. These studies define a hierarchical organization within the tendon, extending from fibril assembly to fascicle formation. Correlation of different levels of extracellular compartmentalization with tissue architecture provides insight into the cellular controls involved in collagen fibril and higher order assembly and a better understanding of how collagen fibrils are collected into structural groups, positioned, and woven into functional tissue-specific collagen macroaggregates.
利用传统电子显微镜和高压电子显微镜研究了鸡胚肌腱成纤维细胞形成胶原纤维、纤维束以及组织特异性胶原大聚集体的过程。在鸡肌腱形态发生过程中,至少有三个细胞外区室负责三个层次的基质组织:胶原纤维、纤维束和胶原大聚集体。我们的观察结果表明,胶原纤维形成过程中最初的细胞外事件发生在狭窄的细胞质凹陷内,推测是在细胞的紧密调控下进行的。胶原纤维在这些与细胞外空间相连的深而窄的凹陷内形成。当这些狭窄的凹陷与细胞表面融合时,细胞表面会变得高度卷曲,出现褶皱和突起,包裹着正在形成的纤维束。这些纤维束横向结合并融合,在第三个由细胞界定的细胞外区室内形成聚集体。我们的解释是,随着细胞突起缩回,细胞质在纤维束之间缩回,第三个区室形成。这些研究确定了肌腱内的层次结构,从纤维组装到束状结构形成。不同层次的细胞外区室化与组织结构的相关性,有助于深入了解参与胶原纤维和更高层次组装的细胞控制机制,并更好地理解胶原纤维是如何被收集到结构组中、定位并编织成功能性组织特异性胶原大聚集体的。