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淋巴因子不会直接激活液相C3。

No direct activation of fluid phase C3 by lymphokines.

作者信息

Kirchhoff W, Sorg C

出版信息

Z Immunitatsforsch Immunobiol. 1977 Feb;152(5):431-7.

PMID:842071
Abstract

Supernatants of stimulated (PPD or Con A) or unstimulated guinea pig lymph node cell cultures in serum-free medium were fractionated on Sephadex G 75. The fractions were tested for C3-consuming activities in a hemolytical assay. No C3 consumption could be detected in any fraction (MW range 80,000 to 10,000). The same result was obtained by extending the fractionation range using Sephadex G 200. A lytic activity with a molecular weight of appr. 225,000 which lysed EAC 14 cells in the presence of C2, 5, 6, 7, 8, 9 was attributed to serum C3 contaminating the cultures. It was determined that C3 is not produced in significant amounts by lymphocyte cultures.

摘要

将无血清培养基中经刺激(结核菌素纯蛋白衍生物或刀豆蛋白A)或未经刺激的豚鼠淋巴结细胞培养物的上清液在葡聚糖G 75上进行分级分离。通过溶血试验检测各分级分离物的补体C3消耗活性。在任何分级分离物(分子量范围80,000至10,000)中均未检测到补体C3消耗。使用葡聚糖G 200扩大分级分离范围也得到了相同结果。在存在补体成分C2、5、6、7、8、9的情况下,一种分子量约为225,000的裂解活性可裂解EAC 14细胞,该活性归因于污染培养物的血清补体C3。经测定,淋巴细胞培养物不会大量产生补体C3。

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