Department of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
J Invest Dermatol. 2011 Apr;131(4):892-9. doi: 10.1038/jid.2010.420. Epub 2011 Jan 13.
Fibroproliferative scars are an important clinical problem, and yet the mechanisms that regulate scar formation remain poorly understood. This study explored the hypothesis that the epithelium has a critical role in dictating scar formation, and that these interactions differ in skin and mucosa. Paired skin and vaginal mucosal wounds on New Zealand white (NZW) rabbits diverged significantly; the cutaneous epithelium exhibited a greater and prolonged response to injury when compared with the mucosa. Microarray analysis of the injured epithelium was performed, and numerous factors were identified that were more strongly upregulated in skin, including several proinflammatory cytokines and profibrotic growth factors. Analysis of the underlying mesenchymal tissue demonstrated a fibrotic response in the dermis of the skin but not the mucosal lamina propria, in the absence of a connective tissue injury. To determine if the proinflammatory factors produced by the epidermis may have a role in dermal fibrosis, an IL-1 receptor antagonist was administered locally to healing skin wounds. In the NZW rabbit model, blockade of IL-1 signaling was effective in preventing hypertrophic scar formation. These results support the idea that soluble factors produced by the epithelium in response to injury may influence fibroblast behavior and regulate scar formation in vivo.
纤维增生性瘢痕是一个重要的临床问题,但调节瘢痕形成的机制仍知之甚少。本研究探讨了一个假设,即上皮在决定瘢痕形成中起着关键作用,这些相互作用在皮肤和黏膜中有所不同。新西兰白兔(NZW)的配对皮肤和阴道黏膜伤口明显不同;与黏膜相比,皮肤上皮对损伤的反应更大且持续时间更长。对受伤上皮进行了微阵列分析,发现许多因子在皮肤中被强烈上调,包括几种促炎细胞因子和促纤维化生长因子。对下面的间充质组织的分析表明,在没有结缔组织损伤的情况下,皮肤的真皮出现了纤维化反应,但黏膜固有层没有。为了确定表皮产生的促炎因子是否可能在真皮纤维化中起作用,局部给予白细胞介素 1 受体拮抗剂治疗愈合的皮肤伤口。在 NZW 兔模型中,阻断白细胞介素 1 信号通路可有效预防肥大性瘢痕形成。这些结果支持这样一种观点,即上皮细胞在受伤后产生的可溶性因子可能影响成纤维细胞的行为并调节体内瘢痕形成。