Suzuki S, Ota Y, Ozawa K, Imamura T
POLA R&D Laboratories, Totsuka-ku Yokohama, Japan.
J Invest Dermatol. 2000 Mar;114(3):456-63. doi: 10.1046/j.1523-1747.2000.00912.x.
As the result of alternative mRNA splicing, Fgf-5, the gene encoding fibroblast growth factor-5, translates to both long and short forms of the protein, respectively, designated fibroblast growth factor-5 and fibroblast growth factor-5S. We previously showed that localization of fibroblast growth factor-5 and the level of fibroblast growth factor-5S in murine skin are hair-cycle dependent. In this study, we examined the effect of fibroblast growth factor-5 and fibroblast growth factor-5S on the hair growth cycle in mice. Once the anagen phase of the hair growth cycle was induced in the dorsal skin by depilation during telogen, and effects of subcutaneous injection of fibroblast growth factor-5 and fibroblast growth factor-5S into the affected region were analyzed. We found that fibroblast growth factor-5 inhibited hair growth during anagen and promoted the transition from anagen to catagen. Interestingly, whereas fibroblast growth factor-5S alone exerted no effect on hair growth, it significantly inhibited the catagen-promoting activity of fibroblast growth factor-5 when the two proteins were injected simultaneously. Because neither fibroblast growth factor-5 nor fibroblast growth factor-5S affected skin thickness, it is postulated that changes in skin thickness during hair cycle are separately regulated by factors other than those regulating hair and follicle growth. The present results, together with our earlier findings that fibroblast growth factor-5-producing cells gather around dermal papillae during catagen, whereas fibroblast growth factor-5S is abundantly expressed in the hair follicles only during the latter half of anagen, suggests that the mouse hair growth cycle is regulated by the two Fgf-5 gene products acting in concert: fibroblast growth factor-5 induces catagen, whereas fibroblast growth factor-5S antagonizes this activity during anagen.
由于可变mRNA剪接,编码成纤维细胞生长因子5的基因Fgf-5分别翻译成长、短两种形式的蛋白质,即成纤维细胞生长因子5和成纤维细胞生长因子5S。我们之前发现,成纤维细胞生长因子5在小鼠皮肤中的定位以及成纤维细胞生长因子5S的水平与毛发生长周期相关。在本研究中,我们检测了成纤维细胞生长因子5和成纤维细胞生长因子5S对小鼠毛发生长周期的影响。在休止期通过拔毛诱导背部皮肤进入生长期后,分析了在受影响区域皮下注射成纤维细胞生长因子5和成纤维细胞生长因子5S的效果。我们发现,成纤维细胞生长因子5在生长期抑制毛发生长,并促进从生长期向退行期的转变。有趣的是,单独注射成纤维细胞生长因子5S对毛发生长没有影响,但当两种蛋白质同时注射时,它能显著抑制成纤维细胞生长因子5促进退行期的活性。由于成纤维细胞生长因子5和成纤维细胞生长因子5S均不影响皮肤厚度,因此推测毛发生长周期中皮肤厚度的变化是由调控毛发和毛囊生长以外的其他因素单独调节的。本研究结果与我们之前的发现一致,即在退行期,产生成纤维细胞生长因子5的细胞聚集在毛乳头周围,而成纤维细胞生长因子5S仅在生长期后半段在毛囊中大量表达,这表明小鼠毛发生长周期受两种Fgf-5基因产物协同作用的调控:成纤维细胞生长因子5诱导退行期,而成纤维细胞生长因子5S在生长期拮抗这种活性。