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培养的视网膜毛细血管周细胞产生胶原蛋白。

Collagen production by cultured retinal capillary pericytes.

作者信息

Cohen M P, Frank R N, Khalifa A A

出版信息

Invest Ophthalmol Vis Sci. 1980 Jan;19(1):90-4.

PMID:7350139
Abstract

The cells that proliferate from microvessels isolated from calf retinas and placed in tissue culture have been found to derive from the intramural pericytes. When these cells were cultured in medium supplemented with ascorbate and pulsed for 24 hr with [14C]proline, about 2% of the [14C]proline in the nondialyzable protein secreted into the culture medium by these cells was hydroxylated, and about 10% of the incorporated [4C]proline was solubilized by purified collagenase. Agarose gel chromatography of the postculture media showed that unreduced [14C]collagen polypeptides were recovered in large-molecular-weight aggregates (greater than 300,000 daltons) which were largely converted to chains of approximately 95,000 molecular weight and some dimers and trimers of MW approximately 180,000 and 270,000 when the medium was subjected to reduction and alkylation prior to chromatography. The findings indicate that cultured retinal pericytes elaborate collagen and suggest the production of type III collagen. Retinal microvessel cells in culture may facilitate study of abnormalities in retinal pericyte function and collagen synthesis that occur in retinal vascular diseases.

摘要

已发现从小牛视网膜分离并置于组织培养中的微血管增殖的细胞来源于壁内周细胞。当这些细胞在添加抗坏血酸的培养基中培养并用[14C]脯氨酸脉冲处理24小时时,这些细胞分泌到培养基中的不可透析蛋白质中约2%的[14C]脯氨酸被羟化,并且约10%掺入的[4C]脯氨酸被纯化的胶原酶溶解。培养后培养基的琼脂糖凝胶色谱显示,未还原的[14C]胶原多肽在大分子聚集体(大于300,000道尔顿)中回收,当培养基在色谱分析前进行还原和烷基化时,这些聚集体大部分转化为分子量约为95,000的链以及一些分子量约为180,000和270,000的二聚体和三聚体。这些发现表明培养的视网膜周细胞能合成胶原,并提示其产生III型胶原。培养的视网膜微血管细胞可能有助于研究视网膜血管疾病中发生的视网膜周细胞功能和胶原合成异常。

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