Moll I, Paus R, Moll R
Department of Dermatology, Mannheim Medical School, University of Heidelberg, Mannheim, Germany.
J Invest Dermatol. 1996 Feb;106(2):281-6. doi: 10.1111/1523-1747.ep12340714.
The distribution and antigen expression of Merkel cells in mouse skin is as yet ill defined. Since the mouse offers an excellent model for studying the origin and functions of Merkel cells, the Merkel cell distribution as well as the expression of intermediate filament proteins and neuronal markers was characterized in C57 BL/6 mouse skin by immunohistochemistry and electron microscopy. Merkel cells in whisker pads, back, and foot pad skin as identified by staining for neuron-specific enolase-an established neuroendocrine marker--expressed cytokeratins (CK) 8,18, and 20 (i.e., simple-epithelial CKs), but not CKs 4 and 13. Sequential double staining for neuron-specific enolase and CK 20 showed consistent co-expression in Merkel cells, establishing CK 20 as a specific immunocytochemical marker for mouse Merkel cells. The Merkel cells also were immunoreactive for synaptophysin but not for neurofilament proteins, peripherin, S-100 protein, and neural cell adhesion molecule. Using CK 8, 18, and 20 as markers, we detected many Merkel cells in the outer roots sheath of vibrissae hair follicles and in foot pad skin. However, only few Merkel cells were found in back skin. These were restricted to small clusters, localized basally within the Haarscheiben epidermis of tylotrich hair follicles, and formed close contacts to prominent nerve fiber terminals as shown by electron microscopy. In striking contrast to human skin, Merkel cells were never found in the epithelium of pelage hair follicles. Even more strikingly, the density of Haarscheiben-associated Merkel cells changed substantially during the highly synchronized, depilation-induced C 57 BL/6 hair cycle, with a minimum in back skin with all hair follicles in telogen or catagen, and a maximum in back skin with all hair follicles in anagen IV-VI. These observations on the Merkel cell hair cycle-dependent distribution in murine skin point to important differences in Merkel cell functions between humans and mice, and raise intriguing questions as to the role of Merkel cells in hair biology.
默克尔细胞在小鼠皮肤中的分布和抗原表达尚未明确。由于小鼠是研究默克尔细胞起源和功能的优秀模型,因此通过免疫组织化学和电子显微镜对C57 BL/6小鼠皮肤中的默克尔细胞分布以及中间丝蛋白和神经元标志物的表达进行了表征。通过对神经元特异性烯醇化酶(一种已确立的神经内分泌标志物)进行染色鉴定,发现触须垫、背部和脚垫皮肤中的默克尔细胞表达细胞角蛋白(CK)8、18和20(即简单上皮CK),但不表达CK4和13。对神经元特异性烯醇化酶和CK20进行连续双重染色显示,默克尔细胞中存在一致的共表达,从而确立CK20为小鼠默克尔细胞的特异性免疫细胞化学标志物。默克尔细胞对突触素也有免疫反应,但对神经丝蛋白、外周蛋白、S-100蛋白和神经细胞黏附分子没有反应。以CK8、18和20作为标志物,我们在触须毛囊的外根鞘和脚垫皮肤中检测到许多默克尔细胞。然而,在背部皮肤中仅发现少数默克尔细胞。这些细胞局限于小簇,位于触须毛囊的Haarscheiben表皮基部,并与突出的神经纤维终末形成紧密接触,电子显微镜显示了这一点。与人类皮肤形成鲜明对比的是,在被毛毛囊的上皮中从未发现默克尔细胞。更引人注目的是,在高度同步的、脱毛诱导的C57 BL/6毛发周期中,与Haarscheiben相关的默克尔细胞密度发生了显著变化,在所有毛囊处于休止期或退行期的背部皮肤中密度最低,而在所有毛囊处于生长期IV-VI的背部皮肤中密度最高。这些关于小鼠皮肤中默克尔细胞毛发周期依赖性分布的观察结果表明,人类和小鼠的默克尔细胞功能存在重要差异,并引发了关于默克尔细胞在毛发生物学中作用的有趣问题。