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[角膜细胞间基质大分子生物合成的调节]

[Regulation of the biosynthesis of macromolecules of the intercellular corneal matrix].

作者信息

Menasche M, Junqua S, Payrau P, Robert L

出版信息

Pathol Biol (Paris). 1975 Nov;23(9):705-9.

PMID:177927
Abstract

The influence of a 1M CaCl2 extract and of a collagenase digest of corneal stroma of the biosynthesis of the macromolecules of corneal stroma was investigated. Calf corneas were incubated "in vitro" with radioactive tracers (14C-L-proline; 3H-D-glucosamine or 35SO4) in the presence or absence of the above extracts. After incubation the corneas are submitted to a fractional extraction in order to separate the major macromolecular fractions of the stroma. An increase in incorporation of all tracers is observed in the 1M CaCl2 (CTC), TCA and urea-extracts (containing resp. the diffusible macromolecules, proteoglycans, polymeric collagen and structural glycoproteins) in the presence of the macromolecular extracts and also with the collagenase-hydrolysate of cornea. These results show the existence of a stimulation of the biosynthesis of intracellular matrix macromolecules of the cornea by corneal extracts, probably through positive "feedback" type of mechanism.

摘要

研究了1M氯化钙提取物和角膜基质胶原酶消化物对角膜基质大分子生物合成的影响。将小牛角膜在有或没有上述提取物的情况下与放射性示踪剂(14C-L-脯氨酸;3H-D-葡糖胺或35SO4)进行“体外”孵育。孵育后,对角膜进行分级提取,以分离基质的主要大分子组分。在大分子提取物存在的情况下以及角膜胶原酶水解产物存在时,在1M氯化钙(CTC)、三氯乙酸(TCA)和尿素提取物(分别含有可扩散大分子、蛋白聚糖、聚合胶原和结构糖蛋白)中观察到所有示踪剂掺入增加。这些结果表明,角膜提取物可能通过正“反馈”类型的机制刺激角膜细胞内基质大分子的生物合成。

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