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探索维甲酸诱导脱发的发病机制:全反式维甲酸通过上调毛乳头中转化生长因子-β2诱导毛囊过早进入退行期(休止期)。

Towards dissecting the pathogenesis of retinoid-induced hair loss: all-trans retinoic acid induces premature hair follicle regression (catagen) by upregulation of transforming growth factor-beta2 in the dermal papilla.

作者信息

Foitzik Kerstin, Spexard Tanja, Nakamura Motonobu, Halsner Ursula, Paus Ralf

机构信息

Department of Dermatology, University Hospital Hamburg-Eppendorf, University of Hamburg, Hamburg, Germany.

出版信息

J Invest Dermatol. 2005 Jun;124(6):1119-26. doi: 10.1111/j.0022-202X.2005.23686.x.

Abstract

Diffuse hair loss ranks among the most frequent and psychologically most distressing adverse effects of systemic therapy with retinoids, which severely limits their therapeutic use even where clinically desired. Since the underlying mechanisms of retinoid-induced effluvium are as yet unknown, we have investigated the influence of the prototypic retinoid all-trans retinoic acid (ATRA, tretinoin) on the growth of human scalp hair follicles (HF) in culture. HF in the anagen VI stage of the hair cycle were cultured in the presence of 10(-8) or 10(-10) M ATRA. Compared with controls, hair shaft elongation declined significantly already after 2 d in the ATRA-treated group, and approximately 80% of the ATRA-treated HF had prematurely entered catagen-like stage at day 6, compared with 30% in the control group. This corresponded to an upregulation of apoptotic and a downregulation of Ki67-positive cells in ATRA-treated HF. Since transforming growth factor (TGF)-beta has been implicated as a key inducer of catagen, we next studied whether ATRA treatment had any effect on follicular expression. TGF-beta2 immunoreactivity was detected in the outer root sheath of anagen VI scalp HF. In catagen follicles, TGF-beta2 was also expressed in the regressing epithelial strand. After 4 d of ATRA treatment, TGF-beta2 was significantly upregulated in anagen HF in the dermal papilla (DP) and the dermal sheath, 7, and TGF-beta neutralizing antibody partially abrogated at RA induced hair growth inhibition. Real-time PCR confirmed a significant upregulation of TGF-beta2 transcripts in ATRA-treated hair bulbs. This study is the first to provide direct evidence that ATRA can indeed induce a catagen-like stage in human HF and suggests that this occurs, at least in part, via upregulation of TGF-beta2 in the DP. Therefore, topical TGF-beta2/TGF-beta receptor II antagonists deserve to be explored for the prevention and management of retinoid-induced hair loss.

摘要

弥漫性脱发是维甲酸全身治疗最常见且在心理上最令人苦恼的不良反应之一,这严重限制了它们在临床上即使有需求时的治疗应用。由于维甲酸诱导脱发的潜在机制尚不清楚,我们研究了原型维甲酸全反式维甲酸(ATRA,维甲酸)对培养的人头皮毛囊(HF)生长的影响。处于毛发生长周期生长期VI期的毛囊在10(-8)或10(-10) M ATRA存在下培养。与对照组相比,ATRA处理组在2天后毛干伸长就显著下降,并且在第6天,约80%接受ATRA处理的毛囊过早进入类似退行期,而对照组为30%。这对应于ATRA处理的毛囊中凋亡上调和Ki67阳性细胞下调。由于转化生长因子(TGF)-β被认为是退行期的关键诱导因子,我们接下来研究ATRA处理是否对毛囊表达有任何影响。在生长期VI期头皮毛囊的外根鞘中检测到TGF-β2免疫反应性。在退行期毛囊中,TGF-β2也在退化的上皮索中表达。ATRA处理4天后,生长期毛囊的真皮乳头(DP)和真皮鞘中的TGF-β2显著上调,并且TGF-β中和抗体部分消除了维甲酸诱导的毛发生长抑制。实时PCR证实ATRA处理的毛球中TGF-β2转录本显著上调。本研究首次提供直接证据表明ATRA确实可在人毛囊中诱导类似退行期,并且表明这至少部分是通过DP中TGF-β2的上调发生的。因此,局部应用TGF-β2/TGF-β受体II拮抗剂值得探索用于预防和治疗维甲酸诱导的脱发。

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