Orlova T G, Mamontova T V, Mentkevich L M, Gulevich N E, Soloviev V D
Acta Virol. 1980 Dec;24(6):421-6.
Calcium chloride stimulated virus-induced production of leukocyte interferon by human and animal blood and haemopoietic organ cells. CaCl2 treatment of surviving cells (leukocytes, human and mouse bone marrow) and Namalva cells was the most effective when carried out simultaneously with adsorption of the virus-inducer or when CaCl2 pretreatment was combines with its subsequent addition together with the virus-inducer. Optimal CaCl2 concentrations were 5 mM for human bone marrow cells and 10 mM for human leukocytes and mouse bone marrow cells. CaCl2 treatment was equivalent to priming in case of interferon induction in human leukocytes and, as distinct from priming, it considerably increased virus-induced interferon production by Namalva cells.
氯化钙可刺激人和动物血液及造血器官细胞产生病毒诱导的白细胞干扰素。当氯化钙处理存活细胞(白细胞、人和小鼠骨髓细胞)以及纳马勒瓦细胞时,与病毒诱导剂吸附同时进行,或者将氯化钙预处理与其随后与病毒诱导剂一起添加相结合时,效果最为显著。人骨髓细胞的最佳氯化钙浓度为5 mM,人白细胞和小鼠骨髓细胞的最佳浓度为10 mM。在人白细胞干扰素诱导的情况下,氯化钙处理等同于引发作用,与引发作用不同的是,它显著增加了纳马勒瓦细胞病毒诱导的干扰素产量。