Ito Chikako, Saitoh Yuko, Fujita Yasuko, Yamazaki Yoshimitsu, Imamura Toru, Oka Syuichi, Suzuki Satoshi
Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan.
J Cell Physiol. 2003 Nov;197(2):272-83. doi: 10.1002/jcp.10369.
Earlier studies demonstrated that knock-out of fibroblast growth factor-5 gene (Fgf-5) prolonged anagen VI phase of hair cycle, resulting long hairs in the mice. We showed the activities on hair growth of the two Fgf-5 gene products, one of which, FGF-5 suppressed hair growth by inhibiting anagen proceeding and inducing the transition from anagen to catagen, and FGF-5S, a shorter polypeptide with FGF-5-antagonizing activity translated from alternatively spliced mRNA, suppressed this activity of FGF-5. As the results suggested that FGF-5 antagonist would increase hair growth, we synthesized various peptides having partial sequences of human FGF-5 and FGF-5S and determined their FGF-5 antagonist activity. Among them, a decapeptide designated P3 (95-VGIGFHLQIY-104) that aligns with receptor binding sites of FGF-1 and FGF-2 suppressed FGF-5-induced proliferation of BALB/3T3 A31 and NIH/3T3 murine fibroblasts, and FGF receptor-1c (FGFR-1c)-transfected Ba/F3 cell line (FR-Ba/F3 cells). IC50s of this peptide on these cell proliferations were 64, 28, 146 microM, respectively. On the other hand, IC50 of this peptide on binding of FGF-5 to the FGFR-1(IIIc)/Fc chimera was 483 microM. Examination in dorsal depilated mice revealed that the P3 peptide reduced the activity of FGF-5 to recover hair pigmentation and hair follicle lengths. The classification of histologically observed skin sections showed FGF-5-induced delations of anagen procedure had reduced by the P3 peptide. The anti-Ki67 antibody staining of hair follicles was inhibited by administration of FGF-5, and this inhibition by FGF-5 was recovered by administration of the P3 peptide. The P3 peptide alone did not affect hair follicle length and hair cell proliferation. These results indicate that the decapeptide antagonized FGF-5 activity in vivo, and reduced the inhibition of FGF-5 in hair growth, confirming that FGF-5 inhibitors are promising substances against hair loss and/or for promoting hair growth.
早期研究表明,敲除成纤维细胞生长因子5基因(Fgf-5)可延长毛发生长周期的生长期VI期,使小鼠长出长毛。我们展示了两种Fgf-5基因产物对毛发生长的作用,其中一种,FGF-5通过抑制生长期进程并诱导从生长期向退行期转变来抑制毛发生长,而FGF-5S是一种由选择性剪接的mRNA翻译而来的具有FGF-5拮抗活性的较短多肽,可抑制FGF-5的这种活性。由于结果表明FGF-5拮抗剂会促进毛发生长,我们合成了具有人FGF-5和FGF-5S部分序列的各种肽,并测定了它们的FGF-5拮抗活性。其中,一种名为P3(95-VGIGFHLQIY-104)的十肽与FGF-1和FGF-2的受体结合位点对齐,可抑制FGF-5诱导的BALB/3T3 A31和NIH/3T3小鼠成纤维细胞以及FGF受体-1c(FGFR-1c)转染的Ba/F3细胞系(FR-Ba/F3细胞)的增殖。该肽对这些细胞增殖的IC50分别为64、28、146微摩尔。另一方面,该肽对FGF-5与FGFR-1(IIIc)/Fc嵌合体结合的IC50为483微摩尔。在背部脱毛小鼠中的研究表明,P3肽降低了FGF-5恢复毛发色素沉着和毛囊长度的活性。组织学观察的皮肤切片分类显示,P3肽减少了FGF-5诱导的生长期进程的延长。FGF-5给药可抑制毛囊的抗Ki67抗体染色,而P3肽给药可恢复FGF-5的这种抑制作用。单独使用P3肽不影响毛囊长度和毛细胞增殖。这些结果表明,该十肽在体内拮抗FGF-5活性,并减少了FGF-5对毛发生长的抑制作用,证实FGF-5抑制剂是有前景的抗脱发和/或促进毛发生长的物质。