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首页> 外文期刊>The Journal of investigative dermatology. >Kallikrein-related peptidase 8-dependent skin wound healing is associated with upregulation of kallikrein-related peptidase 6 and PAR2
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Kallikrein-related peptidase 8-dependent skin wound healing is associated with upregulation of kallikrein-related peptidase 6 and PAR2

机译:激肽释放酶相关肽酶8依赖性皮肤伤口愈合与激肽释放酶相关肽酶6和PAR2的上调相关

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摘要

Kallikrein-related peptidase 8 (KLK8) is believed to be involved in the maintenance of skin homeostasis and pathogenesis of inflammatory skin diseases. Although previous studies have shown that KLK8 is expressed around incisional wounds, the exact role of KLK8 in wound healing remains obscure. In the present study, we compared wound healing in wild-type (WT) and Klk8 gene-disrupted (kallikrein-related peptidase 8 knockout, Klk8 /) mouse skin. Wound healing in Klk8 /mice was hampered with defective keratinocyte proliferation, differentiation, and migration in the early stages of wound healing. Compared with the prominent induction of Klk6 and protease-activated receptor 2 (PAR2) messenger RNA, and protein in WT mice after wounding, a much lower increase was observed in Klk8 /skin. After skin wounding in WT mice, increased Klk6 was detected from the upper stratum spinosum to the stratum corneum. Moreover, in WT mice, Klk6 protein was processed. PAR2 was diffusely expressed in the cytoplasm of the stratum spinosum at day 7 post wounding in WT mice. These results suggest that Klk8 is involved in the proliferation and migration of keratinocytes through the upregulation and activation of Klk6 in the early stages of wound healing, and possibly in keratinocyte differentiation associated with the upregulation and activation of PAR2 in the late stages of wound healing.
机译:激肽释放酶相关肽酶8(KLK8)被认为与皮肤稳态和炎症性皮肤病的发病机理有关。尽管先前的研究表明KLK8在切开伤口周围表达,但KLK8在伤口愈合中的确切作用仍然不清楚。在本研究中,我们比较了野生型(WT)和Klk8基因中断(激肽释放酶相关肽酶8敲除,Klk8 /)小鼠皮肤的伤口愈合情况。在伤口愈合的早期,Klk8 /小鼠的伤口愈合受到不良的角质形成细胞增殖,分化和迁移的阻碍。与受伤后野生型小鼠中Klk6和蛋白酶激活受体2(PAR2)信使RNA和蛋白质的显着诱导相比,在Klk8 /皮肤中观察到的增幅要低得多。在WT小鼠皮肤受伤后,从棘上层到角质层检测到Klk6增加。此外,在野生型小鼠中,加工了Klk6蛋白。在WT小鼠受伤后第7天,PAR2在棘肌层的细胞质中弥散表达。这些结果表明,Klk8在伤口愈合的早期阶段通过Klk6的上调和激活参与角质形成细胞的增殖和迁移,并可能在伤口愈合的后期与PAR2的上调和激活相关的角质形成细胞分化。

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