Zheng Z M, Specter S C, Lancz G
Department of Medical Microbiology & Immunology, College of Medicine, University of South Florida, Tampa 33612, USA.
Immunol Invest. 1995 Aug;24(5):737-56. doi: 10.3109/08820139509060702.
Tumor necrosis factor alpha (TNF-alpha) is most commonly produced by macrophages stimulated by lipopolysaccharide (LPS). The present study shows that BSA in place of FBS in RPMI 1640 medium accelerated the rate of LPS-induced TNF-alpha production by resident peritoneal macrophages from BALB/c mice when compared to LPS in serum free medium. Using 10 or 100 ng LPS/ml and 100 U IFN-gamma/ml in RPMI 1640 medium plus 0.5% BSA, both cytoplasmic TNF-alpha mRNA and TNF-alpha precursor and extracellular TNF-alpha production by mouse macrophages were increased when compared to stimulation by LPS plus IFN-gamma in medium without BSA and FBS. The level of TNF-alpha produced was shown to be related to the BSA concentration. Medium containing BSA but no LPS also stimulated macrophages to produce TNF-alpha, but BSA's TNF-alpha inducing activity varied among different lots and was not blocked by polyclonal antibody to BSA. This effect appeared to be associated with the presence of immunoglobulin in BSA products. Confirmation that BSA activity was not due to LPS contamination was achieved by testing macrophages from LPS-nonresponder C3H/HeJ mice, as well as testing TNF-alpha induction in the presence of polymyxin B (10 micrograms/ml), an LPS inhibitor.
肿瘤坏死因子α(TNF-α)最常见于由脂多糖(LPS)刺激的巨噬细胞产生。本研究表明,与无血清培养基中的LPS相比,在RPMI 1640培养基中用牛血清白蛋白(BSA)代替胎牛血清(FBS)可加速BALB/c小鼠腹腔常驻巨噬细胞产生LPS诱导的TNF-α的速率。在含有0.5% BSA的RPMI 1640培养基中使用10或100 ng LPS/ml和100 U IFN-γ/ml,与在不含BSA和FBS的培养基中用LPS加IFN-γ刺激相比,小鼠巨噬细胞的细胞质TNF-α mRNA、TNF-α前体以及细胞外TNF-α的产生均增加。所产生的TNF-α水平显示与BSA浓度相关。含有BSA但不含LPS的培养基也刺激巨噬细胞产生TNF-α,但BSA的TNF-α诱导活性在不同批次间有所不同,且不受抗BSA多克隆抗体的阻断。这种效应似乎与BSA产品中免疫球蛋白的存在有关。通过检测LPS无反应性C_{3}H/HeJ小鼠的巨噬细胞,以及在存在LPS抑制剂多粘菌素B(10微克/毫升)的情况下检测TNF-α诱导,证实了BSA的活性不是由于LPS污染所致。