Mitrovic D R
Am J Anat. 1977 Oct;150(2):333-47. doi: 10.1002/aja.1001500207.
The histogenesis and mechanism of joint clefting of the developing chick embryo up to the fifteenth day of incubation have been studied morphologically, ultrastructurally, and by histochemical methods. Cell degeneration was consistently noted 24 hours after differentiation of the joint tissue, and it is postulated that this early cell necrosis might account for the loosening of the medial part of articular mesenchyme (interzone) leading to differentiation of a three-layered embryonic joint. At the time of joint clefting degenerative cells were also seen in the peripheral parts of the developing articular cavity. In some cases clefting was immediately preceded and/or accompanied by the appearance of elongated, basophilic and electron-opaque cells closely arranged along the zone of tissue cleavage. These cells were thought to be implicated in some way in the clefting process and later to constitute a surface cell layer of articular cartilage. In addition to these observations clear morphological and histoautoradiographic evidence was found for the presence of an organic component, presumably mucopolysaccharide, in the primitive synovial fluid. Fluid secretion might also account for tissue cleavage at the sites of its accumulation. The data reported here suggest that joint cavity formation results from a combination of both intrinsic, genetically expressed and extrinsic mechanical factors acting synchronously.
运用形态学、超微结构及组织化学方法,对孵化至第15天的发育中鸡胚关节裂隙的组织发生及机制进行了研究。在关节组织分化24小时后,持续观察到细胞变性,据推测,这种早期细胞坏死可能是导致关节间充质(中间带)内侧部分松解的原因,从而促使三层胚胎关节的分化。在关节裂隙形成时,在发育中的关节腔周边部分也可见到变性细胞。在某些情况下,裂隙形成之前和/或同时,会出现沿组织裂隙带紧密排列的细长、嗜碱性且电子不透明的细胞。这些细胞被认为在某种程度上与裂隙形成过程有关,随后构成关节软骨的表面细胞层。除了这些观察结果外,还发现了明确的形态学和组织放射自显影证据,表明原始滑液中存在一种有机成分,推测为粘多糖。液体分泌也可能是其积聚部位组织裂隙形成的原因。本文报道的数据表明,关节腔的形成是内在的、基因表达的因素与外在机械因素同步作用的结果。