Vielkind U, Sebzda M K, Gibson I R, Hardy M H
Department of Biomedical Sciences, University of Guelph, Ontario, Canada.
Acta Anat (Basel). 1995;152(2):93-109. doi: 10.1159/000147688.
In order to explore the origin and significance of Merkel cells in the hairy skin of mammals, the development of Merkel cells and nerve endings in the dorsolateral skin of C57BL mouse embryos was studied in serial cryostat sections. At 13 and 14 days of gestation, application of a monoclonal antibody to mouse keratin 8 (mK8) resulted in specific immunofluorescence of all cells in the epidermis and periderm. The periderm retained specific staining until it was shed, around 18 days. At 15 days, mK8-specific staining elsewhere was restricted to scattered immature Merkel cells in the developing tylotrich follicles and the adjacent epidermis. Between 16 and 17 days, these cells assembled within the basal epidermal layer, caudal to each tylotrich follicle, to form a disc-shaped rudiment of a 'haarscheibe' or touch dome. No Merkel cells were found in association with the later developing awl and zigzag follicles. In mice homozygous or hemizygous for the Tabby mutation, in which tylotrich follicles never form, no Merkel cells were found in any part of the dorsolateral skin. In mice homozygous for the recessive downy mutation, in which all three types of hair are present but reduced in size, Merkel cell development was the same as in wild-type mice. Nerve endings were located in the upper dermal mesenchyme by a monoclonal antibody to neural cell adhesion molecule. This antibody also stained plasma membranes in specific parts of the hair follicles during their development. From 14 to 19 days, none of the nerve endings were seen in contact with the epidermis or the follicle epithelium, even in areas where Merkel cells were located. These findings support the view that both location and early differentiation of Merkel cells in the dorsolateral epidermis are independent of neural influences but linked to the development of tylotrich follicles.
为了探究哺乳动物有毛皮肤中默克尔细胞的起源及意义,我们利用连续冰冻切片技术,对C57BL小鼠胚胎背外侧皮肤中默克尔细胞和神经末梢的发育进行了研究。在妊娠第13天和第14天,应用针对小鼠角蛋白8(mK8)的单克隆抗体,可使表皮和周皮中的所有细胞产生特异性免疫荧光。周皮在大约18天时脱落前一直保持特异性染色。在第15天,其他部位的mK8特异性染色仅限于发育中的触须毛囊和相邻表皮中散在的未成熟默克尔细胞。在第16天至17天之间,这些细胞在每个触须毛囊尾部的基底表皮层内聚集,形成一个盘状的“触盘”或触觉穹顶雏形。未发现默克尔细胞与后来发育的锥状毛和锯齿状毛囊相关联。在携带Tabby突变的纯合或半合子小鼠中,触须毛囊从未形成,其背外侧皮肤的任何部位均未发现默克尔细胞。在携带隐性绒毛突变的纯合子小鼠中,所有三种毛发类型均存在但尺寸减小,默克尔细胞的发育与野生型小鼠相同。通过针对神经细胞黏附分子的单克隆抗体,可将神经末梢定位在上皮真皮间充质中。该抗体在毛囊发育过程中也会对毛囊特定部位的质膜进行染色。从第14天至19天,即使在默克尔细胞所在区域,也未观察到神经末梢与表皮或毛囊上皮接触。这些发现支持了这样一种观点,即背外侧表皮中默克尔细胞的位置和早期分化均独立于神经影响,但与触须毛囊的发育相关。