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In vitro reproduction of the catagen like apoptosis on the hair follicle keratinocytes

机译:毛囊角质形成细胞在体外的催化作用如细胞凋亡的繁殖

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We have previously reported that in the catagen phase apoptotic cells increased, compared with those in the anagen phase. Although many groups have tried to reveal the mechanism of induction of apoptosis, this is still unclear because there is no method to reproduce the catagen like apoptosis (CLA) on the hair follicle keratinocytes (HFK) in vitro. In this report, to induce the CLA on the HFK, we have examined whether apoptosis occurred on the HFK by disruption of attachment to the culture dish. Moreover, the effect of the caspase inhibitors on the CLA induced by such method was examined. The HFK were cultured on agarose coated dish for complete suspension culture and fragmentated DNA was analyzed. Fragmentated DNA was also analyzed after addition of the caspase inhibitors to this suspension culture. As the results, fragmentated DNA from the HFK cultured on the agarose coated dish was increased, compared with that on the type I collagen coated dish. Moreover, fragmentated DNA was completely disappeared by addition of the caspasel/caspasel like protease inhibitor. All these results suggest that, in part, the CLA may be reproduced on the HFK by disruption of attachment to the culture dish and some caspases may regulate apoptosis in the catagen phase.
机译:我们先前已经报道过,在生长期,与生长期相比,凋亡细胞增加。尽管许多研究小组试图揭示诱导细胞凋亡的机制,但仍不清楚,因为尚无方法可在体外毛囊角质形成细胞(HFK)上复制类似催化的细胞凋亡(CLA)。在此报告中,为了诱导HFK上的CLA,我们已经检查了通过破坏培养皿的附着力在HFK上是否发生了凋亡。此外,研究了胱天蛋白酶抑制剂对通过这种方法诱导的CLA的作用。将HFK在琼脂糖包被的培养皿中培养以进行完全悬浮培养,并分析片段化的DNA。将半胱天冬酶抑制剂加入该悬浮培养物中后,还分析了片段化的DNA。结果,与在I型胶原蛋白包被的培养皿上培养的HFK相比,来自HFK的片段化DNA增加了。此外,通过加入卡斯帕瑟/卡斯帕瑟样蛋白酶抑制剂,使片段化的DNA完全消失。所有这些结果表明,通过破坏培养皿的附着力,CLA可能部分在HFK上复制,某些胱天蛋白酶可能调节催化期的细胞凋亡。

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