Petiot Anita, Conti Francesco J A, Grose Richard, Revest Jean-Michel, Hodivala-Dilke Kairbaan M, Dickson Clive
Cancer Research UK, London Research Institute, 61 Lincoln's Inn Fields, London WC2A 3PX, UK.
Development. 2003 Nov;130(22):5493-501. doi: 10.1242/dev.00788.
To understand the role Fgf signalling in skin and hair follicle development, we analysed the phenotype of mice deficient for Fgfr2-IIIb and its main ligand Fgf10. These studies showed that the severe epidermal hypoplasia found in mice null for Fgfr2-IIIb is caused by a lack of the basal cell proliferation that normally results in a stratified epidermis. Although at term the epidermis of Fgfr2-IIIb null mice is only two to three cells thick, it expresses the classical markers of epidermal differentiation and establishes a functional barrier. Mice deficient for Fgf10 display a similar but less severe epidermal hypoplasia. By contrast, Fgfr2-IIIb-/-, but not Fgf10-/-, mice produced significantly fewer hair follicles, and their follicles were developmentally retarded. Following transplantation onto nude mice, grafts of Fgfr2-IIIb-/- skin showed impaired hair formation, with a decrease in hair density and the production of abnormal pelage hairs. Expression of Lef1, Shh and Bmp4 in the developing hair follicles of Fgfr2-IIIb-/- mice was similar to wild type. These results suggest that Fgf signalling positively regulates the number of keratinocytes needed to form a normal stratified epidermis and to initiate hair placode formation. In addition, Fgf signals are required for the growth and patterning of pelage hairs.
为了解Fgf信号在皮肤和毛囊发育中的作用,我们分析了Fgfr2-IIIb及其主要配体Fgf10基因缺失小鼠的表型。这些研究表明,Fgfr2-IIIb基因敲除小鼠中发现的严重表皮发育不全是由于缺乏正常情况下导致分层表皮的基底细胞增殖所致。尽管足月时Fgfr2-IIIb基因敲除小鼠的表皮只有两到三层细胞厚,但它表达表皮分化的经典标志物并建立了功能屏障。Fgf10基因缺失的小鼠表现出类似但不太严重的表皮发育不全。相比之下,Fgfr2-IIIb-/-小鼠(而非Fgf10-/-小鼠)产生的毛囊明显减少,且其毛囊发育迟缓。将Fgfr2-IIIb-/-皮肤移植到裸鼠上后,毛发形成受损,毛发密度降低且出现异常被毛。Fgfr2-IIIb-/-小鼠发育中的毛囊中Lef1、Shh和Bmp4的表达与野生型相似。这些结果表明,Fgf信号正向调节形成正常分层表皮和启动毛基板形成所需的角质形成细胞数量。此外,Fgf信号是被毛生长和模式形成所必需的。