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ASK1-dependent recruitment and activation of macrophages induce hair growth in skin wounds

机译:依赖ASK1的巨噬细胞募集和激活诱导皮肤伤口中的毛发生长

摘要

Apoptosis signal-regulating kinase 1 (ASK1) is a member of the mitogen-activated protein 3-kinase family that activates both c-Jun NH2-terminal kinase and p38 pathways in response to inflammatory cytokines and physicochemical stress. We report that ASK1 deficiency in mice results in dramatic retardation of wounding-induced hair regrowth in skin. Oligonucleotide microarray analysis revealed that expression of several chemotactic and activating factors for macrophages, as well as several macrophage-specific marker genes, was reduced in the skin wound area of ASK1-deficient mice. Intracutaneous transplantation of cytokine-activated bone marrow-derived macrophages strongly induced hair growth in both wild-type and ASK1-deficient mice. These findings indicate that ASK1 is required for wounding-induced infiltration and activation of macrophages, which play central roles in inflammation-dependent hair regrowth in skin.
机译:凋亡信号调节激酶1(ASK1)是丝裂原激活的蛋白3激酶家族的成员,该家族激活c-Jun NH2末端激酶和p38通路,以响应炎症细胞因子和理化应激。我们报告说,小鼠中的ASK1缺乏会导致伤口引起的皮肤毛发再生严重延迟。寡核苷酸微阵列分析显示,在ASK1缺陷小鼠的皮肤伤口区域,巨噬细胞的几种趋化因子和活化因子以及几种巨噬细胞特异性标记基因的表达降低。细胞因子激活的骨髓巨噬细胞的皮内移植强烈诱导了野生型和ASK1缺陷型小鼠的毛发生长。这些发现表明,ASK1是伤口诱导的巨噬细胞浸润和活化所必需的,而巨噬细胞在炎症依赖性毛发再生中起着核心作用。

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