Morse H C, Yetter R A, Stimpfling J H, Pitts O M, Fredrickson T N, Hartley J W
Cell. 1985 Jun;41(2):439-48. doi: 10.1016/s0092-8674(85)80017-9.
Some strains of C57BL/10 H-2-congenic mice were found to exhibit greying with age, whereas others did not. Two patterns of greying were observed, diffuse greying beginning at 4 to 6 months of age and patterned greying beginning at 4 to 6 weeks. Strains exhibiting either greying pattern expressed high levels of infectious ecotropic and mink cell focus-inducing murine leukemia viruses (MuLV) in tests of thymus and spleen and in cultures from skin or tail biopsies, whereas nongreying strains expressed little virus until late in life. Electron microscopy demonstrated large accumulations of MuLV in grey, but not in black areas, of skin from a mouse with patterned greying. Infectious MuLV was produced spontaneously by embryos of greying, but not of nongreying, mice and pups of nongreying strains fostered on greying mothers turned grey after 3 months. These results suggest that greying with age results from melanocyte dysfunction that occurs subsequent to pre- or early postnatal infection with MuLV.
发现一些C57BL/10 H-2同源近交系小鼠会随着年龄增长出现毛发变灰的现象,而其他一些则不会。观察到两种毛发变灰的模式,一种是在4至6个月大时开始的弥漫性毛发变灰,另一种是在4至6周时开始的 patterned 毛发变灰。在胸腺和脾脏检测以及皮肤或尾部活检组织培养中,表现出任何一种毛发变灰模式的品系都表达高水平的感染性嗜亲性和貂细胞集落形成诱导性鼠白血病病毒(MuLV),而非毛发变灰的品系在生命后期才表达少量病毒。电子显微镜显示,在一只具有patterned毛发变灰的小鼠的皮肤中,MuLV大量积聚在灰色区域而非黑色区域。毛发变灰的小鼠胚胎会自发产生感染性MuLV,而非毛发变灰的小鼠胚胎则不会,并且由毛发变灰的母鼠哺育的非毛发变灰品系幼崽在3个月后毛发变灰。这些结果表明,随着年龄增长出现的毛发变灰是由于在出生前或出生后早期感染MuLV后发生的黑素细胞功能障碍所致。