Thorogood P, Bee J, von der Mark K
Dev Biol. 1986 Aug;116(2):497-509. doi: 10.1016/0012-1606(86)90150-8.
In the avian embryo a matrix-mediated tissue interaction between retinal pigmented epithelium and neural crest-derived periocular mesenchyme leads to the differentiation of (scleral) cartilage. The composition of the extracellular matrix at the interface between these two tissues has been examined immunohistochemically, both during and after the interaction has taken place. Of the matrix components studied (fibronectin, laminin, and collagen types I, II, IV, and V) only collagen type II displayed a dramatic change in distribution between the two stages. During the interaction, at stage 15, type II was present in the extracellular compartment basal to the epithelium. After completion of the interaction, collagen type II was no longer detectable at the interface even though it was readily detectable in the vitreous humor, cornea, and perinotochordal sheath, and subsequently will be expressed by the chondrogenic tissue itself as overt differentiation commences. These results suggest that collagen type II might be causally involved in this particular epitheliomesenchymal interaction. Examination of the spatial and temporal patterns of collagen type II expression elsewhere in the developing craniofacial complex revealed a hitherto unreported pattern of distribution. In addition to its predictable locations (i.e., cornea, vitreous, and perinotochordal sheath) it was found to be present at certain other sites, for example, at the basal surfaces of some neuroepithelia. These additional locations are all known to be sites of chondrogenesis-promoting tissue interactions which result in the formation of the elements of the cartilaginous neurocranium (e.g., otic vesicle). Furthermore this spatial distribution exhibits a changing temporal pattern in that it is detectable at the time that the interactions are known to be taking place, but subsequently is no longer detectable by the immunohistochemical means employed. This definable pattern of transient collagen type II expression, occurring at very early stages of craniofacial development, is interpreted as reflecting one level of morphogenetic specification of chondrocranial/skull form in the developing vertebrate head.
在鸟类胚胎中,视网膜色素上皮与神经嵴衍生的眼周间充质之间由基质介导的组织相互作用导致(巩膜)软骨的分化。在这种相互作用发生期间及之后,已经通过免疫组织化学方法检查了这两种组织界面处细胞外基质的组成。在所研究的基质成分(纤连蛋白、层粘连蛋白以及I、II、IV和V型胶原)中,只有II型胶原在两个阶段之间的分布发生了显著变化。在相互作用期间,即第15阶段,II型胶原存在于上皮基底的细胞外间隙中。相互作用完成后,即使在玻璃体、角膜和脊索周鞘中很容易检测到II型胶原,但在界面处却不再能检测到,随后随着软骨形成组织开始明显分化,它将由软骨形成组织自身表达。这些结果表明,II型胶原可能与这种特定的上皮间充质相互作用存在因果关系。对发育中的颅面复合体其他部位II型胶原表达的时空模式进行检查,发现了一种迄今未报道的分布模式。除了其可预测的位置(即角膜、玻璃体和脊索周鞘)外,还发现它存在于某些其他部位,例如一些神经上皮的基底表面。所有这些额外的位置都是已知的促进软骨形成的组织相互作用位点,这些相互作用会导致软骨性脑颅(例如耳泡)的元素形成。此外,这种空间分布呈现出变化的时间模式,即在已知相互作用发生时可以检测到,但随后通过所采用的免疫组织化学方法就不再能检测到。这种在颅面发育非常早期阶段出现的可定义的瞬时II型胶原表达模式,被解释为反映了发育中脊椎动物头部软骨脑颅/颅骨形态的一种形态发生特化水平。