Alibardi Lorenzo
Dipartimento di Biologia evoluzionistica sperimentale, University of Bologna, 40126, Bologna, Italy.
J Morphol. 2004 Sep;261(3):345-63. doi: 10.1002/jmor.10254.
The fine structure of hairs in the most ancient extant mammals, the monotremes, is not known. The present study analyzes the ultrastructure and immunocytochemistry for keratins, trichohyalin, and transglutaminase in monotreme hairs and compares their distribution with that present in hairs of the other mammals. The overall ultrastructure of the hair and the distribution of keratins is similar to that of marsupial and placental hairs. Acidic and basic keratins mostly localize in the outer root sheath. The inner root sheath (IRS) comprises 4-8 cell layers in most hairs and forms a tile-like sheath around the hair shaft. No cytological distinction between the Henle and Huxley layers is seen as cells become cornified about at the same time. Externally to the last cornified IRS cells (homologous to the Henle layer), the companion layer contains numerous bundles of keratin. Occasionally, some granules in the companion layer show immunoreactivity for the trichohyalin antibody. This further suggests that the IRS in monotremes is ill-defined, as the companion layer of placental hairs studied so far does not express trichohyalin. A cross-reactivity with an antibody against sheep trichohyalin is present in the IRS of monotremes, suggesting conserved epitopes across mammalian trichohyalin. Trichohyalin granules in the IRS consist of a framework of immunolabeled coarse filaments of 10-12 nm. The latter assume a parallel orientation and lose the immunoreactivity in fully cornified cells. Transglutaminase immunolabeling is diffuse among trichohyalin granules and among the parallel 10-12 nm filaments of maturing inner root cells. Transglutaminase is present where its substrate, trichohyalin, is modified as matrix protein. Cornification of IRS is different from that of hair fiber cuticle and from that of the cornified layer of the epidermis above the follicle. The different consistency among cuticle, IRS, and corneous layer of the epidermis determines separation between hair fiber, IRS, and epidermis. This allows the hair to exit on the epidermal surface after shedding from the IRS and epidermis. Based on comparative studies of reptilian and mammalian skin, a speculative hypothesis on the evolution of the IRS and hairs from the skin of synapsid reptiles is presented.
现存最古老的哺乳动物——单孔目动物毛发的精细结构尚不清楚。本研究分析了单孔目动物毛发中角蛋白、毛透明蛋白和转谷氨酰胺酶的超微结构及免疫细胞化学,并将它们的分布与其他哺乳动物毛发中的分布进行比较。毛发的整体超微结构和角蛋白的分布与有袋类动物和胎盘类动物的毛发相似。酸性和碱性角蛋白大多定位于外根鞘。大多数毛发的内根鞘(IRS)由4 - 8层细胞组成,并在毛干周围形成瓦片状鞘。由于亨勒层和赫胥黎层的细胞几乎同时发生角质化,因此在细胞学上无法区分这两层。在最后角质化的内根鞘细胞(与亨勒层同源)外部,伴随层含有大量角蛋白束。偶尔,伴随层中的一些颗粒对角蛋白抗体呈免疫反应性。这进一步表明单孔目动物的内根鞘定义不明确,因为迄今为止研究的胎盘类动物毛发的伴随层不表达毛透明蛋白。单孔目动物的内根鞘中存在与抗绵羊毛透明蛋白抗体的交叉反应性,这表明哺乳动物毛透明蛋白存在保守表位。内根鞘中的毛透明蛋白颗粒由10 - 12纳米的免疫标记粗丝框架组成。后者呈平行排列,并在完全角质化的细胞中失去免疫反应性。转谷氨酰胺酶免疫标记在毛透明蛋白颗粒之间以及成熟内根细胞的平行10 - 12纳米细丝之间呈弥漫性分布。转谷氨酰胺酶存在于其底物毛透明蛋白被修饰为基质蛋白的部位。内根鞘的角质化不同于毛纤维角质层的角质化以及毛囊上方表皮角质层的角质化。角质层、内根鞘和表皮角质层之间不同的稠度决定了毛纤维、内根鞘和表皮之间的分离。这使得毛发在从内根鞘和表皮脱落之后能够在表皮表面长出。基于对爬行类动物和哺乳动物皮肤的比较研究,提出了一个关于内根鞘和毛发从合弓纲爬行类动物皮肤进化而来的推测性假说。