Stricklin G P, Li L, Nanney L B
Division of Dermatology, Department of Veterans Affairs Medical Center, Nashville, Tennessee 37212.
J Invest Dermatol. 1994 Sep;103(3):352-8. doi: 10.1111/1523-1747.ep12394926.
The process of wound healing sets in motion a complex and dynamic series of events, which includes the remodeling of the extracellular matrix. Degradation of matrix macromolecules is mediated through the actions of the matrix metalloproteinase family. Conversely, the actions of this enzyme family are regulated by tissue inhibitors of metalloproteinases (TIMPs). In this study, we have developed riboprobes derived from human cDNAs representing collagenase, 72-kDa gelatinase, and TIMP and have found them to be sufficiently specific and sensitive for use in in situ hybridization studies of porcine burn wounds. Expression of these mRNAs, although not seen in uninjured skin, was found to be a predictable and locally distinct event in wound repair. Transcripts for collagenase and TIMP but not 72-kDa gelatinase were detected at the resurfacing epithelial margin; label was also detected in and around follicular epithelium within the wound bed. Transcripts for both metalloenzymes and TIMP were found throughout the viable dermis and subcutaneous tissues underlying the wound bed. However, expression of 72-kDa gelatinase was most prominent in the superficial dermis adjacent to the resurfacing epidermis at the wound margin. Collagenase and TIMP transcripts were particularly prominent in a perivascular pattern in the dermis and in the connective tissue network surrounding adipocytes in the subcutaneous zone. Numerous cell types appeared to be involved, including keratinocytes, fibroblasts, macrophages, and endothelial cells. Future exploitation of this porcine thermal injury model is likely to provide information about the spatial and temporal patterns of matrix metalloproteinase and TIMP expression in cutaneous wound healing.
伤口愈合过程启动了一系列复杂且动态的事件,其中包括细胞外基质的重塑。基质大分子的降解是通过基质金属蛋白酶家族的作用介导的。相反,该酶家族的作用受金属蛋白酶组织抑制剂(TIMPs)调节。在本研究中,我们从代表胶原酶、72 kDa明胶酶和TIMP的人cDNA中开发了核糖探针,并发现它们在用于猪烧伤创面的原位杂交研究时具有足够的特异性和敏感性。这些mRNA的表达在未受伤皮肤中未见,但在伤口修复中是一个可预测且局部有差异的事件。在重新上皮化的边缘检测到了胶原酶和TIMP的转录本,但未检测到72 kDa明胶酶的转录本;在创面床内的毛囊上皮及其周围也检测到了标记。在创面床下方的整个存活真皮和皮下组织中都发现了金属酶和TIMP的转录本。然而,72 kDa明胶酶的表达在伤口边缘与重新上皮化表皮相邻的浅表真皮中最为突出。胶原酶和TIMP转录本在真皮中的血管周围模式以及皮下区域脂肪细胞周围的结缔组织网络中尤为突出。似乎有多种细胞类型参与其中,包括角质形成细胞、成纤维细胞、巨噬细胞和内皮细胞。对该猪热损伤模型的进一步研究可能会提供有关皮肤伤口愈合中基质金属蛋白酶和TIMP表达的时空模式的信息。