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碲免疫调节剂AS101诱导毛发生长:与毛囊角质形成细胞的终末分化延迟及KGF表达的ras依赖性上调相关

Hair growth induction by the Tellurium immunomodulator AS101: association with delayed terminal differentiation of follicular keratinocytes and ras-dependent up-regulation of KGF expression.

作者信息

Sredni Benjamin, Gal Rivka, Cohen Ian J, Dazard Jean-Eudes, Givol David, Gafter Uzi, Motro Benny, Eliyahu Siona, Albeck Michael, Lander Harry M, Kalechman Yona

机构信息

C.A.I.R. Institute, Faculty of Life Sciences, Bar Ilan University, Ramat Gan, 52900 Israel.

出版信息

FASEB J. 2004 Feb;18(2):400-2. doi: 10.1096/fj.03-0552fje. Epub 2003 Dec 4.

Abstract

The synthetic immunomodulator AS101[ammonium trichloro(dioxoethylene-o,o')tellurate] was previously found to protect cancer patients from chemotherapy-induced bone marrow toxicity and alopecia. Here we show that AS101 induces hair growth in nude and normal mice. AS101 possesses the dual ability to both induce anagen and retard spontaneous catagen in the C57BL/6 mouse model. Anagen induced by AS101 is mediated by keratinocyte growth factor (KGF), as it is abrogated both in nude mice co-treated with AS101 plus neutralizing anti KGF antibodies and in AS101-treated transgenic mice expressing a dominant-negative KGF receptor transgene in basal keratinocytes. AS101 up-regulates KGF expression by activating the ras signaling pathway in cultured fibroblasts. AS101-induced delayed catagen is associated with inhibition of terminal differentiation marker expression both in nude and C57BL/6 mice epidermal follicular keratinocytes and in cultures of primary mouse follicular keratinocytes induced to differentiate. This activity is associated with relatively sustained elevation of p21waf. Delayed expression of terminal differentiation markers was not induced by AS101 in follicular keratinocytes from p21waf knockout mice. Because similar results were obtained with cultures of primary human keratinocytes and fibroblasts, preliminary case report studies revealed substantial hair growth when AS101 was topically applied on three adolescents who had remained alopeciac 1-2 years after chemotherapy. The results emphasize the unique mode of action of AS101 and highlight its potential clinical use for treating certain types of alopecia.

摘要

合成免疫调节剂AS101[三氯(二氧乙烯-o,o')碲酸铵]先前被发现可保护癌症患者免受化疗引起的骨髓毒性和脱发。在此我们表明,AS101可诱导裸鼠和正常小鼠毛发生长。在C57BL/6小鼠模型中,AS101具有诱导生长期和延缓自发退行期的双重能力。AS101诱导的生长期由角质形成细胞生长因子(KGF)介导,因为在同时接受AS101和中和性抗KGF抗体治疗的裸鼠以及在基底角质形成细胞中表达显性负性KGF受体转基因的AS101处理的转基因小鼠中,这种作用均被消除。AS101通过激活培养的成纤维细胞中的ras信号通路来上调KGF表达。AS101诱导的延迟退行期与裸鼠和C57BL/6小鼠表皮毛囊角质形成细胞以及诱导分化的原代小鼠毛囊角质形成细胞培养物中终末分化标志物表达的抑制有关。这种活性与p21waf的相对持续升高有关。AS101在p21waf基因敲除小鼠的毛囊角质形成细胞中未诱导终末分化标志物的延迟表达。由于原代人角质形成细胞和成纤维细胞培养物也获得了类似结果,初步病例报告研究显示,当将AS101局部应用于三名化疗后1-2年仍脱发的青少年时,毛发生长显著。这些结果强调了AS101独特的作用方式,并突出了其在治疗某些类型脱发方面的潜在临床应用价值。

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