首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Distinct localization of collagenase and tissue inhibitor of metalloproteinases expression in wound healing associated with ulcerative pyogenic granuloma.
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Distinct localization of collagenase and tissue inhibitor of metalloproteinases expression in wound healing associated with ulcerative pyogenic granuloma.

机译:溃疡性化脓性肉芽肿相关的伤口愈合中胶原酶和金属蛋白酶组织抑制剂表达的独特定位。

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摘要

To examine the role of metalloproteinases in tissue remodeling associated with wound healing, we used in situ hybridization to localize the expression of collagenase and tissue inhibitor of metalloproteinases (TIMP) in samples of pyogenic granuloma. Strong hybridization for collagenase mRNA was detected in basal keratinocytes near the advancing edge of all ulcerative lesions, but no collagenase mRNA was seen in samples without ulceration. Distinct from the sites of collagenase expression, TIMP mRNA was detected in stromal cells and in cells surrounding proliferating vessels. No collagenase mRNA was found in the epidermis of healthy skin, although occasional stromal cells contained collagenase or TIMP mRNAs, and TIMP mRNA was detected in hair follicles and sebaceous glands. Our results suggest that basal keratinocytes adjacent to wounded epidermis are critically involved in matrix remodeling, much more so than adjacent or underlying dermal fibroblasts. Furthermore, as several reports have suggested, TIMP may play a role in angiogenesis. Finally, in contrast to findings from other models which indicate that collagenase and TIMP proteins are secreted by the same cells, our data also demonstrate that these proteins can be produced in vivo independently of each other.
机译:为了检查金属蛋白酶在与伤口愈合相关的组织重塑中的作用,我们使用原位杂交定位化脓性肉芽肿样品中胶原酶和金属蛋白酶组织抑制剂(TIMP)的表达。在所有溃疡性病变的前缘附近的基底角质形成细胞中检测到胶原酶mRNA的强杂交,但是在没有溃疡的样品中未观察到胶原酶mRNA。与胶原酶表达部位不同,在基质细胞和增殖血管周围的细胞中检测到TIMP mRNA。在健康皮肤的表皮中未发现胶原酶mRNA,尽管偶尔的基质细胞含有胶原酶或TIMP mRNA,并且在毛囊和皮脂腺中检测到TIMP mRNA。我们的结果表明,邻近受伤表皮的基底角质形成细胞与基质重塑至关重要,远比邻近或下方的真皮成纤维细胞重要。此外,正如一些报道所暗示的,TIMP可能在血管生成中起作用。最后,与其他模型表明胶原酶和TIMP蛋白由同一细胞分泌的发现相反,我们的数据也证明这些蛋白可以彼此独立地在体内产生。

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