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首页> 外文期刊>Experimental Eye Research >Epithelial basement membrane proteins perlecan and nidogen-2 are up-regulated in stromal cells after epithelial injury in human corneas
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Epithelial basement membrane proteins perlecan and nidogen-2 are up-regulated in stromal cells after epithelial injury in human corneas

机译:人角膜上皮损伤后基质细胞中上皮基底膜蛋白perlecan和nidogen-2上调

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摘要

The epithelial basement membrane (BM) is a specialized extracellular matrix that has been shown to have a critical role in corneal development, wound healing, and disease. Although the epithelial BM contributes to corneal homeostasis, relatively little is know about non-epithelial production of its components that may be important in defective regeneration of the epithelial basement membrane associated with opacity after photorefractive keratectomy. The purpose of the current study was to investigate stromal production of corneal epithelial BM proteins in wounded human corneas using immunohistochemistry. A total of five unwounded control eyes and five 30-min epithelial-wounded corneas were obtained from fresh corneoscleral buttons removed from human eyes enucleated due to choroidal melanoma with normal anterior segments. In the wounded corneas, an eight mm patch of central corneal epithelium and epithelial BM was removed with a Beaver blade when the patient was under general anesthesia. Immunohistochemical analyses were performed to detect perlecan and nidogen-2 proteins important components of the epithelial BM lamina lucida and lamina densa zones. Perlecan and nidogen-2 proteins were detected in the BM itself and at low levels in keratocytes in all unwounded corneas. After epithelial injury, both perlecan and nidogen-2 were expressed at high levels in stromal keratocytes, including superficial keratocytes in the early phases of apoptosis. Thus, after epithelial and epithelial BM injury, stromal keratocytes contribute important perlecan and nidogen-2 components to the regenerating epithelial BM. (C) 2015 Elsevier Ltd. All rights reserved.
机译:上皮基底膜(BM)是一种特殊的细胞外基质,已被证明在角膜发育,伤口愈合和疾病中具有关键作用。尽管上皮BM有助于角膜动态平衡,但对其成分的非上皮产生知之甚少,这可能对光折射角膜切除术后不透明引起的上皮基底膜再生不良有重要意义。本研究的目的是使用免疫组织化学研究受伤的人角膜中角膜上皮BM蛋白的基质产生。从因患有脉络膜黑色素瘤且前节正常的人摘除的新鲜角膜巩膜纽扣中摘除新鲜角膜巩膜纽扣,共获得五只未受伤的对照眼和五只30分钟上皮受伤的角膜。在受伤的角膜中,当患者处于全身麻醉状态时,用Beaver刀片切除了8毫米的中央角膜上皮和上皮BM斑块。进行了免疫组织化学分析,以检测上皮BM lucina和lamina densa区的重要成分perlecan和nidogen-2蛋白。在所有未受伤的角膜中,BM本身和角膜细胞中的Perlecan和nidogen-2蛋白均检出。上皮损伤后,在凋亡的早期阶段,perlecan和nidogen-2在基质角化细胞(包括浅层角化细胞)中高水平表达。因此,在上皮和上皮BM损伤后,基质角膜细胞为再生的上皮BM贡献了重要的perlecan和nidogen-2成分。 (C)2015 Elsevier Ltd.保留所有权利。

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