首页> 外文期刊>Archives of dermatological research. >T-oligos as differential modulators of human scalp hair growth and pigmentation: a new 'time lapse system' for studying human skin and hair follicle biology in vitro?
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T-oligos as differential modulators of human scalp hair growth and pigmentation: a new 'time lapse system' for studying human skin and hair follicle biology in vitro?

机译:T-寡核苷酸作为人类头皮毛发生长和色素沉着的差异调节剂:一种新的“延时系统”,用于在体外研究人类皮肤和毛囊的生物学?

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Small DNA oligonucleotides homologous to the 3' overhang of human telomeres, called T-oligos, stimulate pigmentation in human epidermal melanocytes in vitro and in vivo. They induce UV-mimetic effects in the absence of DNA-damage, however, it is unknown how T-oligos affect human hair follicle keratinocyte and melanocyte functions in situ. Here, we present the first evidence that these oligonucleotides are powerful modulators of pigmentation and growth of microdissected, organ-cultured human scalp hair follicles. Hair follicles were incubated with T-oligo or vehicle control and were then assessed for changes in hair shaft length, follicle morphology, pigmentation, proliferation and apoptosis. After only 48 h, T-oligos induced a fourfold increase in pigmentation of human anagen VI hair bulbs, while hair matrix keratinocyte proliferation was reduced by 65%, without apparent changes in hair bulb cell apoptosis. This corresponded well with a significant inhibition of hair shaft elongation, which was not accompanied by premature catagen induction in anagen VI hair follicles. These diametrically opposed effects of T-oligos on human hair follicle melanocytes (stimulation of melanogenesis) versus human hair bulb keratinocytes (inhibition of proliferation) in situ illustrate that human hair follicle organ culture offers an excellent tool for T-oligo research. They suggest that T-oligos deserve to be further explored for the management of clinical hair growth and pigmentation disorders, and raise the possibility that this model may offer a unique "time lapse system" for studying skin and hair follicle biology and DNA repair strategies under physiologically relevant conditions.
机译:与人类端粒3'突出端同源的小DNA寡核苷酸,称为T-寡核苷酸,在体外和体内刺激人表皮黑素细胞中的色素沉着。它们在不破坏DNA的情况下诱导紫外线模拟作用,但是,未知T寡核苷酸如何影响人的毛囊角质形成细胞和黑素细胞功能。在这里,我们提供了第一个证据,这些寡核苷酸是色素沉着和微解剖,器官培养的人类头皮毛囊生长的强有力的调节剂。将毛囊与T-oligo或溶媒对照一起孵育,然后评估毛干长度,毛囊形态,色素沉着,增殖和凋亡的变化。仅48小时后,T-寡核苷酸诱导人类生长期VI毛发灯泡的色素沉着增加了四倍,而毛发基质角质形成细胞的增殖减少了65%,而毛发灯泡的细胞凋亡没有明显变化。这与显着抑制发干伸长相吻合,在生长期VI毛囊中并未伴有过早的催化作用。 T-寡核苷酸对人毛囊黑素细胞(刺激黑素生成)与人毛球角质形成细胞(抑制增殖)的原本相反的作用说明,人毛囊器官培养为T-寡核苷酸研究提供了极好的工具。他们认为,应进一步探索T-寡核苷酸来治疗临床毛发生长和色素沉着障碍,并提高这种模型为研究皮肤和毛囊生物学以及DNA修复策略提供独特的“延时系统”的可能性。生理相关条件。

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