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Cellular events during scar-free skin regeneration in the spiny mouse, Acomys

机译:在无疤痕皮肤再生细胞活动Acomys带刺的鼠标

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摘要

In contrast to the lab mouse, Mus musculus, several species of spiny mouse, Acomys, can regenerate epidermis, dermis, hairs, sebaceous glands with smooth muscle erector pili muscles and skeletal muscle of the panniculus carnonsus after full thickness skin wounding. Here, we have compared the responses of these scarring and nonscarring organisms concentrating on the immune cells and wound cytokines, cell proliferation, and the collagenous components of the wound bed and scar. The blood of Acomys is very neutropenic but there are greater numbers of mast cells in the Acomys wound than the Mus wound. Most importantly there are no F4/80 macrophages in the Acomys wound and many proinflammatory cytokines are either absent or in very low levels which we suggest may be primarily responsible for the excellent regenerative properties of the skin of this species. There is little difference in cell proliferation in the two species either in the epidermis or mesenchymal tissues but the cell density and matrix composition of the wound is very different. In Mus there are 8 collagens which are up-regulated at least 5-fold in the wound creating a strongly trichrome-positive matrix whereas in Acomys there are very few collagens present and the matrix shows only light trichrome staining. The major component of the Mus matrix is collagen XII which is up-regulated between 10 and 30-fold after wounding. These results suggest that in the Acomys wound the absence of many cytokines resulting in the lack of macrophages is responsible for the failure to up-regulate fibrotic collagens, a situation which permits a regenerative response within the skin rather than the generation of a scar.
机译:实验室的老鼠相比,亩,几个种类的带刺的鼠标,Acomys,可以再生表皮,真皮,毛发,皮脂与平滑肌腺毛肌的肌肉和骨骼肌脂carnonsus后全厚皮肤受伤。相比这些疤痕的反应nonscarring生物集中免疫伤口细胞和细胞因子、细胞增殖、创面的胶原成分和疤痕。但是有更多的肥大细胞比亩Acomys伤口伤口。重要的是没有F4/80巨噬细胞Acomys伤口和许多促炎细胞因子要么缺失或在非常低的水平吗建议可能主要负责优秀的皮肤的再生能力这个物种。两个物种的扩散表皮细胞或间充质组织但密度和基质成分的伤口非常不同的。哪些是差异至少5倍创建强烈trichrome-positive伤口矩阵而Acomys很少有它现在和矩阵只显示灯三色的染色。亩矩阵是第十二胶原蛋白差异受伤后10至30倍。结果表明,在Acomys伤口没有许多细胞因子导致的缺乏的巨噬细胞的失败负责调控的纤维胶原蛋白,一个情况允许在皮肤的再生反应而不是一代的疤痕。

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