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Cyclosporine A stimulated hair growth from mouse vibrissae follicles in an organ culture model

机译:在器官培养模型中环孢菌素A刺激了小鼠触须毛囊的毛发生长

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摘要

Hypertrichosis is one of the most common side effects of systemic cyclosporine A therapy. It has been previously shown that cyclosporine A induces anagen and inhibits catagen development in mice. In the present study, to explore the mechanisms of cyclosporine A, we investigated the effects of cyclosporine A on hair shaft elongation, hair follicle cell proliferation, apoptosis, and mRNA expression of selected growth factors using an organ culture model of mouse vibrissae. In this model, cyclosporine A stimulated hair growth of normal mouse vibrissae follicles by inhibiting catagen-like development and promoting matrix cell proliferation. In addition, cyclosporine A caused an increase in the expression of vascular endothelial growth factor (VEGF), hepatocyte growth factor (HGF), and nerve growth factor (NGF), and inhibited follistatin expression. Our findings provide an explanation for the clinically observed effects of cyclosporine A on hair growth. The mouse vibrissae organ culture offers an attractive model for identifying factors involved in the modulation of hair growth.
机译:高毛发症是系统性环孢霉素A治疗最常见的副作用之一。先前已经表明,环孢菌素A在小鼠中诱导毛发生长素并抑制催化作用的发展。在本研究中,为探索环孢菌素A的机制,我们使用小鼠触须的器官培养模型研究了环孢菌素A对毛干伸长,毛囊细胞增殖,凋亡和所选生长因子的mRNA表达的影响。在此模型中,环孢菌素A通过抑制类似催化原的发育并促进基质细胞增殖来刺激正常小鼠触须毛囊的毛发生长。此外,环孢霉素A引起血管内皮生长因子(VEGF),肝细胞生长因子(HGF)和神经生长因子(NGF)的表达增加,并抑制了卵泡抑素的表达。我们的发现为临床上观察到的环孢素A对头发生长的影响提供了解释。小鼠触须器官培养提供了一种有吸引力的模型,可用于识别参与头发生长调节的因素。

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