Necrosulfonamide 可促进毛发生长,改善 DHT 引起的毛发生长抑制。

IF 4.6
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引用次数: 0

摘要

背景介绍脱发会影响患者的外观和心理。混系激酶域样假激酶(MLKL)介导的坏死在多种皮肤病中发挥作用,但其对毛发生长的影响尚不清楚:研究MLKL对毛发生长的影响及其调控机制,并确定Necrosulfonamide(NSA,一种MLKL靶向抑制剂)在促进毛发生长和对抗二氢睾酮(DHT)抑制毛发生长方面的潜在临床价值:方法:检测雄激素性脱发(AGA)患者头皮和小鼠皮肤组织中 MLKL 的表达水平。方法:检测雄激素性脱发(AGA)患者头皮和小鼠皮肤组织中 MLKL 的表达水平:结果:在AGA患者中,脱发区域的MLKL表达升高。在小鼠中,MLKL在毛囊的外根鞘细胞中明显表达,在毛发生长期达到高峰。在小鼠皮肤中敲除 MLKL 的表达可促进毛发生长。NSA 通过 Wnt 信号传导促进毛发生长并防止毛囊退化。减少 MLKL 可促进 ORS 细胞增殖,但不会直接影响 DPCs 的生长。有趣的是,当 NSA 与 ORS 细胞共同培养时,它能促进 DPCs 的增殖和诱导。此外,NSA 还能减轻 DHT 对体内和体外毛发生长的抑制作用:结论:NSA抑制了ORS细胞中MLKL的活化,促进了DPC细胞中Wnt信号的活化,改善了DHT对毛发生长的抑制作用,揭示了一种新的脱发机制,有助于抗脱发药物的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Necrosulfonamide promotes hair growth and ameliorates DHT-induced hair growth inhibition

Background

Alopecia affects patients' appearance and psychology. Mixed-lineage kinase domain-like pseudokinase (MLKL)-mediated necroptosis plays a role in various skin diseases, but its effect on hair growth is unclear.

Objective

To investigate the effects of MLKL on hair growth and its regulatory mechanisms and to determine the potential clinical value of Necrosulfonamide (NSA, a MLKL-targeting inhibitor) in promoting hair growth and counteracting dihydrotestosterone (DHT) inhibition of hair growth.

Methods

The expression level of MLKL was detected in the scalp of androgenetic alopecia (AGA) patients and the skin tissues of mice. Knock down MLKL expression or use NSA to observe hair growth in vivo and in vitro.

Results

In AGA patients, MLKL expression is elevated in the alopecia areas. In mice, MLKL is significantly expressed in the outer root sheath (ORS) cells of hair follicles, peaking during the catagen phase. Knockdown expression of MLKL in mice skin promoted hair growth. NSA enhanced hair growth and prevented hair follicle regression via the Wnt signaling. Reduced MLKL boosts ORS cell proliferation without directly impacting DPCs' growth. Interestingly, NSA boosts DPCs' proliferation and induction when co-cultured with ORS cells. Besides, NSA alleviated the inhibition of DHT on hair growth in vivo and vitro.

Conclusion

NSA inhibited the activation of MLKL in ORS cells, promoted the activation of Wnt signal in DPC cells, and improved the inhibition of hair growth by DHT, illuminating a new alopecia mechanism and aiding anti-alopecia drug development.

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