雏鸟羽羽中发育中的倒刺和小枝的细胞结构:倒刺脊形态发生在羽毛进化中的中心作用。

L Alibardi
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引用次数: 0

摘要

目前的超微结构研究显示了细胞如何组织形成鸡胚胎羽绒的复杂结构。羽丝顶端的胚胎表皮向内折叠形成向羽基部延伸的倒刺脊。倒刺脊表皮细胞的层状结构保持不变,但基底层失去了大部分生发活性。羽丝生长的新细胞主要产生于羽丝基部。在倒刺脊中,只有胚胎表皮的最初四层表皮层保留下来形成羽毛:1)外周皮,2)三至五层羽毛鞘和倒刺叶片脊细胞,3)下周皮细胞,4)基部或圆柱形细胞。周皮、鞘、倒刺叶脊和柱状细胞仅合成α -角蛋白。相反,外周层的细胞合成一种小类型的角蛋白:羽毛角蛋白。在孵化时,鸡皮肤的大部分区域(无鳞和有鳞)的下表皮层消失,取而代之的是含有α -角蛋白(卵泡间无鳞表皮)、鳞-角蛋白(鳞片)、喙-角蛋白(喙)和爪-角蛋白(爪)的细胞。只有在羽毛中,原始的近周层细胞保留下来,并形成倒刺和小枝细胞。倒刺叶片脊细胞的存在允许形成分离的倒刺和小枝细胞链,这些细胞在倒刺和小枝细胞合并的细胞之间起间隔作用。下周皮细胞伸长并合并成合囊,形成小枝和倒刺。当小枝和倒刺细胞积聚羽毛角蛋白时,倒刺叶片和圆柱形细胞积聚脂质、囊泡和少量α角蛋白。这些细胞最终因坏死而退化,在小枝和倒刺之间留下空隙和脂质。外鞘溶解后,羽毛的倒刺和小枝的雕刻过程与细胞凋亡无关。事实上,滋养羽毛纤维顶端的血管的收缩决定了羽毛的缺氧,并最终导致羽毛的所有细胞坏死。当鞘、倒刺叶片和圆柱形细胞退化时,形成倒刺和小枝的角化合胞体简单地保留在原地,形成羽毛的分支。倒刺脊的形成被认为是羽毛起源所必需的进化创新。古代始祖动物表皮管状外生物中倒刺脊的形态发生过程是一种进化上的新现象,是真正的鸟类和兽脚亚目动物的特征。倒刺脊的形态发生决定了倒刺和小枝细胞的当代形成是一个独特而不可分割的过程,因此只有倒刺而没有小枝的中间形式的进化羽毛是不可能的。倒刺脊可以与一个大脊合并(轴)或成为分支脊,这一过程是羽状羽毛进化的起源过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell structure of developing barbs and barbules in downfeathers of the chick: Central role of barb ridge morphogenesis for the evolution of feathers.

The present ultrastructural study shows how cells organize to form the complex structure of downfeathers in chick embryos. The embryonic epidermis of the apical part of feather filaments folds inward forming barb ridges which extend toward the base of the feather. The stratification of epidermal cells in barb ridges is maintained but the basal layer loses most of the germinal activity. New cells for the growth of feather filaments are mainly produced in its basal part. In barb ridges only the original four epidermal layers of the embryonic epidermis remain to form feathers: 1) the external periderm, 2) three-five layers of the feather sheath and barb vane ridge cells, 3) subperiderm cells, and 4) basal or cylindrical cells. Periderm, sheath, barb vane ridge and cylindrical cells synthesize only alpha-keratin. Instead, cells of the subperiderm layer synthesize a small type of beta-keratin: feather beta-keratin. At hatching, the subperiderm layer is lost in most areas of the skin of the chick (apteric and scaled), and is replaced by cells containing alpha-keratin (interfollicular-apteric epidermis), scale beta-keratin (scales), beak beta-keratin (beak), and claw beta-keratin (claws). Only in feathers, cells of the original subperiderm layer remain and give origin to barb and barbule cells. The formation of separated chains of barb and barbule cells is allowed by the presence of barb vane ridge cells that function as spacers between merging cells of barb and barbule cells. Subperiderm cells elongate and merge into a syncitium to form barbules and barbs. While barbule and barb cells accumulate feather-keratin, barb vane and cylindrical cells accumulate lipids, vesicles and little alpha-keratin. These cells eventually degenerate by necrosis leaving empty spaces and lipids between barbules and barbs. No apoptosis is necessary to explain the process of carving out of barb and barbules in feathers after dissolution of the external sheath. In fact, the retraction of blood vessels nourishing the apical part of the feather filament determines anoxia and eventually necrosis of all cells of the feather. While sheath, barb vane and cylindrical cells degenerate, the keratinized syncitium forming barbs and barbules simply remain in place to form the ramifications of feathers. The formation of barb ridges is considered as the evolutionary innovation necessary for the origin of feathers. The evolution of the morphogenetic process of barb ridge formation within epidermal tubular outgrowths of the integument of ancient archosaurians was an evolutionary novelty, a true avian and theropod characteristic. Barb ridges morphogenesis determines the contemporary formation of barb and barbule cells as a unique and inseparable process so that intermediate forms of evolving feathers with only barbs but not barbules are unlikely. Barb ridges can merge with a large ridge (rachis) or into branched ridges, a process which was at the origin of the ramogenic process from which pennaceous feathers evolved.

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