Alibardi L, Knapp L W, Sawyer R H
Department of Evolutionary and Experimental Biology, University of Bologna, Italy.
J Submicrosc Cytol Pathol. 2006 Jun-Sep;38(2-3):175-92.
Beta-keratins form large part of the corneous material of scales and feathers. The present immunocytochemical study describes the fine distribution of scale- and feather-keratins (beta-keratins) in embryonic scales of the alligator and in avian embryonic feathers. In embryonic scales of the alligator both scale-keratin and feather-keratin can be immunolocalized, especially in the subperiderm layer. No immunolabeling for feather keratin is instead present in the adult scale after the embryonic epidermis is lost. The embryonic epidermis of feather folds into barb ridges while subperiderm or subsheath cells are displaced into two barbule plates joined to the central ramus. Subperiderm cells react with an antibody against feather keratin and with lower intensity with an antibody against scale keratin. The axial plate is colonized by barb ridge vane cells, which surround subperiderm cells that become barb/barbule cells. The latter cells merge into a branched syncitium and form the micro ramification of feathers. The lengthening of barbule cells derives from the polymerization of feather keratin into long bundles coursing along the main axis of cells. Keratin bundles in feather cells are however ordered in parallel rows while those of scales in both alligator and birds are irregularly packed. This observation indicates a different modality of aggregation and molecular structure between the feather keratin of subperiderm cells versus that of barbule/barbs. Barb vane ridge cells among barbule cells degenerate at late stage of feather development leaving spaces that separate barbules. Barb vane ridge cells contain alpha-keratin and lipids, but not beta-keratin. Cells of marginal plates do not contain beta-keratin, and later degenerate allowing the separation of barbs. The latter become isolated only after sloughing of the sheath, which cells contain bundle of keratin not reactive for both scale- and feather-keratin antibodies. The study confirms morphological observations and shows that subperiderm or subsheath cells differentiate into barb and barbule cells. The morphogenesis of barb ridges has to be considered as an evolutionary novelty that permitted the evolution of feathers from a generalized archosaurian embryonic epidermis.
β -角蛋白构成鳞片和羽毛角质物质的大部分。目前的免疫细胞化学研究描述了鳄鱼胚胎鳞片和鸟类胚胎羽毛中鳞片角蛋白和羽毛角蛋白(β -角蛋白)的精细分布。在鳄鱼胚胎鳞片中,鳞片角蛋白和羽毛角蛋白都可以进行免疫定位,尤其是在亚表皮层。相反,在胚胎表皮消失后的成年鳞片中,没有羽毛角蛋白的免疫标记。羽毛的胚胎表皮折叠成羽枝嵴,而亚表皮或亚鞘细胞则被挤入与中央羽轴相连的两个羽小枝板中。亚表皮细胞与抗羽毛角蛋白抗体发生反应,与抗鳞片角蛋白抗体的反应强度较低。轴向板被羽枝嵴羽片细胞占据,这些细胞围绕着变成羽枝/羽小枝细胞的亚表皮细胞。后者细胞融合成一个分支的合胞体并形成羽毛的微分支。羽小枝细胞的延长源于羽毛角蛋白聚合成沿着细胞主轴排列的长束。然而,羽毛细胞中的角蛋白束排列成平行行,而鳄鱼和鸟类鳞片中的角蛋白束则不规则堆积。这一观察结果表明,亚表皮细胞的羽毛角蛋白与羽小枝/羽枝的羽毛角蛋白在聚集方式和分子结构上存在差异。羽小枝细胞中的羽片嵴细胞在羽毛发育后期退化,留下分隔羽小枝的空间。羽片嵴细胞含有α -角蛋白和脂质,但不含β -角蛋白。边缘板的细胞不含β -角蛋白,随后退化,使羽枝分离。只有在鞘脱落之后,羽枝才会分离,鞘细胞含有对角蛋白鳞片和羽毛角蛋白抗体均无反应的角蛋白束。该研究证实了形态学观察结果,并表明亚表皮或亚鞘细胞分化为羽枝和羽小枝细胞。羽枝嵴的形态发生必须被视为一种进化上的新奇事物,它使得羽毛能够从广义的祖龙胚胎表皮进化而来。