Département de Biomédecine Vétérinaire, Faculté de Médecine Vétérinaire, Université de Montréal, QC, Canada.
Wound Repair Regen. 2011 Mar-Apr;19(2):250-9. doi: 10.1111/j.1524-475X.2010.00663.x.
As a transient hypoxic state exists within skin wounds in horses and may be important for the healing process, this study sought to identify a molecular hypoxia response occurring in horse limb and body wounds healing by second intention. Hypoxia-inducible factor 1α (HIF1α) protein expression was studied throughout repair by Western blotting and immunofluorescence. Paradoxically, HIF1α was strongly expressed in intact skin and its expression decreased dramatically following wounding (p<0.01), despite the expected hypoxic state within the wounded tissue. HIF1α levels reincreased in parallel with the epithelialization process, and more rapidly in body wounds than in limb wounds (p<0.01). HIF1α localized predominantly to the keratinocyte layer, in which it was constitutively expressed throughout healing. The HIF1α target gene cyclin-dependent kinase inhibitor 1A (CDKN1A) showed a pattern of expression similar to HIF1α throughout the healing process and also localized to the keratinocyte layer, suggesting that HIF1α may regulate its constitutive expression. The HIF1α target genes vascular endothelial growth factor A (VEGFA) and solute carrier family 2 (facilitated glucose transporter) member 1 (SLC2A1) however did not have a pattern of expression similar to HIF1α, at the mRNA level. We conclude that HIF1α is expressed in a continuous and hypoxia-independent manner in equine keratinocytes in both intact and wounded skin, and may regulate the expression of CDKN1A in this cell type.
在马的皮肤伤口中存在短暂的缺氧状态,这可能对愈合过程很重要,因此本研究试图确定通过二期愈合的马四肢和身体伤口中发生的分子缺氧反应。通过 Western blot 和免疫荧光法研究了缺氧诱导因子 1α(HIF1α)蛋白在整个修复过程中的表达。矛盾的是,尽管在受伤组织中预期存在缺氧状态,但 HIF1α 在完整的皮肤中强烈表达,并在受伤后急剧下降(p<0.01)。HIF1α 水平与上皮化过程平行增加,在身体伤口中比在四肢伤口中增加得更快(p<0.01)。HIF1α 主要定位于角质形成细胞层,在整个愈合过程中,它在角质形成细胞层中持续表达。HIF1α 的靶基因细胞周期蛋白依赖性激酶抑制剂 1A(CDKN1A)在整个愈合过程中表现出与 HIF1α 相似的表达模式,并且也定位于角质形成细胞层,表明 HIF1α 可能调节其组成型表达。然而,HIF1α 的靶基因血管内皮生长因子 A(VEGFA)和溶质载体家族 2(促进葡萄糖转运体)成员 1(SLC2A1)在 mRNA 水平上没有与 HIF1α 相似的表达模式。我们得出结论,HIF1α 在完整和受伤皮肤的马角质形成细胞中以连续且不依赖缺氧的方式表达,并且可能调节这种细胞类型中 CDKN1A 的表达。