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人皮肤中肌腱蛋白C表达上调与光损伤程度的协同关系。

Coordinate upregulation of tenascin C expression with degree of photodamage in human skin.

作者信息

Filsell W, Rudman S, Jenkins G, Green M R

机构信息

Biosciences Group, Unilever Research, Colworth House, Sharnbrook, Bedford MK44 1LQ, U.K.

出版信息

Br J Dermatol. 1999 Apr;140(4):592-9. doi: 10.1046/j.1365-2133.1999.02756.x.

Abstract

Tenascin C is a large extracellular matrix glycoprotein involved in morphogenesis and wound healing. The distribution and expression levels of tenascin were examined in photodamaged skin to investigate the hypothesis that photoaged skin displays characteristics of wound repair. In situ hybridization and semiquantitative immunohistochemistry were performed on paired skin biopsies from patients with varying levels of photodamage, using monoclonal antibodies and cRNA probes for tenascin and its large isoform. In sun-protected skin, tenascin protein was distributed adjacent to the dermoepidermal junction, usually sparsely and discontinuously; tenascin mRNA was detected in dermal fibroblasts and some keratinocytes. In photodamaged skin, tenascin protein was increased in proportion to the clinical level of photodamage (analysis of variance: P < 0.0001, n = 29). With increased photodamage, tenascin protein expression became continuous along the dermoepidermal junction, extending deeper into and sometimes throughout the papillary dermis; tenascin mRNA was detected throughout the epidermis. Large tenascin isoform protein and mRNA distribution mirrored that of pantenascin, suggesting that it may be the predominant species in photodamaged skin. There was no correlation between tenascin expression levels and age or sex, and no seasonal variation was noted. The results indicate that photodamaged skin demonstrates tenascin increases consistent with an early wound healing response. However, tenascin increases in photodamage appear to be permanent and may therefore interfere with effective repair of ultraviolet-induced damage. In conclusion, this study has shown that dermal tenascin expression increases in proportion to the degree of photodamage. In normal skin, the temporal and spatial patterns of tenascin expression during morphogenesis and tissue remodelling are crucial to their correct progression. In photoageing, the 'normal' control of tenascin expression seems to be abrogated.

摘要

腱生蛋白C是一种大型细胞外基质糖蛋白,参与形态发生和伤口愈合。研究腱生蛋白在光损伤皮肤中的分布和表达水平,以探讨光老化皮肤表现出伤口修复特征这一假说。使用针对腱生蛋白及其大型异构体的单克隆抗体和cRNA探针,对不同光损伤程度患者的配对皮肤活检样本进行原位杂交和半定量免疫组织化学分析。在防晒皮肤中,腱生蛋白分布于真皮表皮交界处附近,通常稀疏且不连续;在真皮成纤维细胞和一些角质形成细胞中检测到腱生蛋白mRNA。在光损伤皮肤中,腱生蛋白的含量与光损伤的临床程度成正比(方差分析:P < 0.0001,n = 29)。随着光损伤加剧,腱生蛋白沿真皮表皮交界处的表达变得连续,深入到乳头层真皮,有时甚至贯穿整个乳头层真皮;在整个表皮中均检测到腱生蛋白mRNA。大型腱生蛋白异构体的蛋白和mRNA分布与总腱生蛋白一致,表明它可能是光损伤皮肤中的主要类型。腱生蛋白的表达水平与年龄或性别无关,也未观察到季节性变化。结果表明,光损伤皮肤中腱生蛋白增加,与早期伤口愈合反应一致。然而,光损伤中腱生蛋白的增加似乎是永久性的,因此可能会干扰紫外线诱导损伤的有效修复。总之,本研究表明真皮腱生蛋白的表达随光损伤程度增加而增加。在正常皮肤中,形态发生和组织重塑过程中腱生蛋白表达的时空模式对其正确进展至关重要。在光老化过程中,腱生蛋白表达的“正常”调控似乎被破坏。

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