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Phospholipase C‐δ1 is an essential molecule downstream ofFoxnl,the gene responsible for the nude mutation, in normal hair development

磷脂酶C 细胞生物学 转染 生物 角蛋白 基因剔除小鼠 效应器 转录因子 化学 信号转导 基因 生物化学 遗传学
作者
Yoshikazu Nakamura,Manabu Ichinohe,Masayuki Hirata,Hirokazu Matsuura,Takashi Fujiwara,Takahiro Igarashi,Masamichi Nakahara,Hideki Yamaguchi,Sadao Yasugi,Tadaomi Takenawa,Kiyoko Fukami
出处
期刊:The FASEB Journal [Wiley]
卷期号:22 (3): 841-849 被引量:55
标识
DOI:10.1096/fj.07-9239com
摘要

Nude mice exhibit athymia and hairlessness by a loss-of-function mutation in the transcription factor Foxn1 gene. Although the immunological functions of Foxn1 have been studied intensively, there have been relatively few studies of its functions in skin. Foxn1 regulates expression of hair keratins, which is essential for normal hair structure; however, how Foxn1 regulates hair keratin expression and hair formation is largely unknown. In the present study, we found that mice lacking phospholipase C (PLC)-delta1, a key molecule in the phosphoinositide signaling pathway, and nude mice show similar hair abnormalities, such as lack of cuticle and bending. We also found that expression of hair keratins was remarkably decreased in skin of PLC-delta1 knockout mice. Furthermore, expression of PLC-delta1 was induced in Foxn1-transfected U2OS cells. In addition, we showed that PLC-delta1 expression was remarkably decreased in skin of nude mice. In skin and keratinocytes of nude mice as well as PLC-delta1 KO mice, activation of PLC downstream effectors, such as PKC and nuclear factor of activated T cells, was impaired. These results indicate that PLC-delta1 is an essential molecule downstream of Foxn1 in normal hair formation, and strongly suggest that hairlessness in nude mice is caused by insufficient expression of PLC-delta1.

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