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补体的第三成分由培养的人内皮细胞转录并分泌。

The third component of complement is transcribed and secreted by cultured human endothelial cells.

作者信息

Warren H B, Pantazis P, Davies P F

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115.

出版信息

Am J Pathol. 1987 Oct;129(1):9-13.

PMID:2444110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1899691/
Abstract

Monotypic cultures of passaged human umbilical vein endothelial cells secrete C3 protein, which is specifically immunoprecipitable from cell lysates and conditioned medium. A transcript migrating at 5.3 kilobases hybridizes with a mouse-derived C3 DNA probe in parallel cultures of endothelial cells, hepatoma cells (HepG2), and freshly isolated human monocytes. Steady-state transcript levels were as follows: HepG2 cells, 1.0; monocytes, 0.05; endothelial cells, 0.01. These data suggest that C3, an indispensible component for activation of complement by both the classical and alternative pathways, is locally synthesized in the vascular bed.

摘要

传代培养的人脐静脉内皮细胞的单型培养物分泌C3蛋白,该蛋白可从细胞裂解物和条件培养基中特异性免疫沉淀。在内皮细胞、肝癌细胞(HepG2)和平行培养的新鲜分离的人单核细胞中,一条迁移率为5.3千碱基的转录本与小鼠来源的C3 DNA探针杂交。稳态转录水平如下:HepG2细胞为1.0;单核细胞为0.05;内皮细胞为0.01。这些数据表明,C3是经典途径和替代途径激活补体的必需成分,在血管床中局部合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/6743541b9487/amjpathol00139-0019-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/69924bfe03d2/amjpathol00139-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/99eb5b4141d9/amjpathol00139-0018-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/3bf9599299a7/amjpathol00139-0018-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/6743541b9487/amjpathol00139-0019-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/69924bfe03d2/amjpathol00139-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/99eb5b4141d9/amjpathol00139-0018-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/3bf9599299a7/amjpathol00139-0018-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff9/1899691/6743541b9487/amjpathol00139-0019-a.jpg

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Quantitative determination of histone modification. H2A acetylation and phosphorylation.组蛋白修饰的定量测定。H2A乙酰化和磷酸化。
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