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豚鼠肝细胞原代培养物对补体第三(C3)、第八(C8)和第九(C9)成分的生物合成。

Biosynthesis of the third (C3), eighth (C8), and ninth (C9) complement components by guinea pig hepatocyte primary cultures.

作者信息

Ramadori G, Tedesco F, Bitter-Suermann D, Meyer zum Büschenfelde K H

出版信息

Immunobiology. 1985 Sep;170(3):203-10. doi: 10.1016/s0171-2985(85)80092-9.

Abstract

In the present report guinea pig hepatocyte primary cultures were established in order to study the synthesis of the eighth (C8) and ninth (C9) complement component. As reference-protein, the third complement component (C3) was measured antigenetically and hemolytically. Synthesis of C8 and C9 was determined by means of the hemolytic activity of the culture supernatant harvested every 24 h during a 6-day incubation period in vitro. The data to be reported demonstrated that the hepatocytes are able to synthesize spontaneously and secrete C8 and C9; in their culture medium a hemolytic activity of about 15-25 X 10(8) em/10(6) cells/24 h for C8 and of 25-90 x 10(8) em/10(6) cells/24 h for C9 were found. The same hepatocyte cultures produced 2500-6000 micrograms/10(6) cells/24 h of C3. Hemolytic C3 activity was also found in the culture media. The synthesis of C8 and C9 could be reversibly inhibited by addition of 30-50 micrograms cycloheximide per ml of culture medium. The kinetics of synthesis show a slight decrease after the first day of culture and a recovery in the following days up to a rate that is two- to threefold higher than that of the first day. The data suggest that hepatocytes could contribute to the production of C8 and C9 present in the plasma.

摘要

在本报告中,为了研究补体第八成分(C8)和第九成分(C9)的合成,建立了豚鼠肝细胞原代培养体系。作为参考蛋白,通过抗原检测法和溶血检测法对第三补体成分(C3)进行了测定。在体外6天的培养期内,每隔24小时收集培养上清液,通过其溶血活性来测定C8和C9的合成。报告的数据表明,肝细胞能够自发合成并分泌C8和C9;在其培养基中,发现C8的溶血活性约为15 - 25×10⁸ em/10⁶细胞/24小时,C9的溶血活性为25 - 90×10⁸ em/10⁶细胞/24小时。同样的肝细胞培养物每24小时可产生2500 - 6000微克/10⁶细胞的C3。在培养基中也发现了溶血C3活性。每毫升培养基中添加30 - 50微克放线菌酮可可逆地抑制C8和C9的合成。合成动力学显示,培养第一天后合成略有下降,随后几天有所恢复,直至达到比第一天高出两到三倍的速率。这些数据表明,肝细胞可能有助于血浆中C8和C9的产生。

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