Anand V, Srivastava L M
Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
Indian J Exp Biol. 1996 Apr;34(4):307-10.
The mouse peritoneal cells (MPS) were stimulated under in vitro and in vivo conditions with different compositions of bovine serum albumin (BSA)-anti BSA immune complexes (IC). The aim was to monitor the biochemical changes that may occur in macrophages and this activation was indicated by an increase in the number and protein content of the cells. The role of these complexes in inducing lysosomal hydrolases release from elicited as well as during an in vitro interaction with ICs was also studied. The insoluble immune complex at equivalence (IC-Eq) and immune complex-antibody excess (IC-Ab) registered a significant increase in number of cells and protein content as compared to soluble immune-complex antigen excess (IC-Ag) complexes. The IC elicited cells showed lesser secretory activity as compared to MPM cells stimulated in vitro. Stimulating capacity of ICs in causing hydrolase release was time and dose dependent. The complement coated complexes were the most effective in inducing enzyme release (4.5-5-fold).
在体外和体内条件下,用不同组成的牛血清白蛋白(BSA)-抗BSA免疫复合物(IC)刺激小鼠腹腔细胞(MPS)。目的是监测巨噬细胞中可能发生的生化变化,细胞数量和蛋白质含量的增加表明了这种激活。还研究了这些复合物在诱导诱导性巨噬细胞释放溶酶体水解酶以及与ICs体外相互作用期间的作用。与可溶性免疫复合物抗原过量(IC-Ag)复合物相比,等价的不溶性免疫复合物(IC-Eq)和免疫复合物-抗体过量(IC-Ab)的细胞数量和蛋白质含量显著增加。与体外刺激的MPM细胞相比,IC诱导的细胞分泌活性较低。ICs引起水解酶释放的刺激能力具有时间和剂量依赖性。补体包被的复合物在诱导酶释放方面最有效(4.5-5倍)。