Kristensen G, Jakobsen P H
Centre for Medical Parasitology, University of Copenhagen, Denmark.
Exp Parasitol. 1996 Mar;82(2):147-54. doi: 10.1006/expr.1996.0019.
Previous studies have indicated the inositol monophosphate (IMP) is a component of the malaria parasite toxin that induces cytokines such as tumour necrosis factor (TNF). To further characterize the toxin we have labeled Plasmodium falciparum in vitro cultures with [14C]inositol or [35S]-methionine and immunoprecipitated the labeled antigens with an antiserum against IMP which blocks malaria parasite-induced TNF production. We detected four proteins associated with IMP when the immunoprecipitates were separated by SDS-PAGE and analyzed by autoradiography. To evaluate the capacity of different P. falciparum antigens to induce cytokine production we separated a mixture of exoantigens by SDS-PAGE gels. Antigen fractions of 43-71 kDa and of a low molecular mass of <20 kDa contained the dominant inducers of TNF alpha interleukin 1 alpha, and interleukin 6 production from human mononuclear cells. The low-molecular-mass antigen fraction contained hemoglobin, while no parasite-specific proteins were detectable when tested by immunoblotting. Hemoglobin may act as a carrier for cytokine-inducing malaria parasite toxins.
先前的研究表明,肌醇单磷酸(IMP)是疟原虫毒素的一个组成部分,该毒素可诱导诸如肿瘤坏死因子(TNF)等细胞因子的产生。为了进一步表征该毒素,我们用[14C]肌醇或[35S]甲硫氨酸标记体外培养的恶性疟原虫,并用抗IMP抗血清免疫沉淀标记的抗原,该抗血清可阻断疟原虫诱导的TNF产生。当通过SDS-PAGE分离免疫沉淀物并通过放射自显影分析时,我们检测到四种与IMP相关的蛋白质。为了评估不同恶性疟原虫抗原诱导细胞因子产生的能力,我们通过SDS-PAGE凝胶分离外抗原混合物。43-71 kDa的抗原组分和分子量<20 kDa的低分子量抗原组分包含来自人单核细胞的TNFα、白细胞介素1α和白细胞介素6产生的主要诱导剂。低分子量抗原组分含有血红蛋白,而通过免疫印迹检测时未检测到寄生虫特异性蛋白质。血红蛋白可能作为细胞因子诱导性疟原虫毒素的载体。