Molina J M, Scadden D T, Byrn R, Dinarello C A, Groopman J E
Division of Hematology/Oncology, New England Deaconess Hospital, Boston, Massachusetts 02215.
J Clin Invest. 1989 Sep;84(3):733-7. doi: 10.1172/JCI114230.
The production of tumor necrosis factor alpha (TNF alpha) and IL-1 beta by the monocytic cell line THP-1, productively infected with HIV-1, was investigated using specific RIA and Northern blot analysis. HIV-infected cells, like uninfected cells, did not constitutively produce any detectable amounts of protein or mRNA for TNF alpha or IL-1 beta. After stimulation with LPS or a combination of LPS plus IFN-gamma, TNF alpha and IL-1 beta were detected in tissue culture supernatants and cell lysates and transcripts for both cytokines were seen on Northern blots. No significant difference in production of these two cytokines was observed between uninfected and chronically infected cells. Acutely HIV-infected cells, however, showed phenotypic changes compatible with maturation and an increase in TNF alpha and IL-1 beta mRNA production, and released significantly higher levels of TNF alpha and IL-1 beta compared with chronically infected or uninfected cells. Furthermore, LPS stimulation of HIV-infected cells increased virus production. These results suggest that HIV-infected monocytic cells may produce increased amounts of TNF alpha and IL-1 beta in response to stimuli that could be present in vivo.
利用特异性放射免疫分析(RIA)和Northern印迹分析,对被HIV-1有效感染的单核细胞系THP-1中肿瘤坏死因子α(TNFα)和白细胞介素-1β(IL-1β)的产生情况进行了研究。与未感染细胞一样,HIV感染的细胞不会组成性地产生任何可检测量的TNFα或IL-1β蛋白或mRNA。在用脂多糖(LPS)或LPS加γ干扰素(IFN-γ)组合刺激后,在组织培养上清液和细胞裂解物中检测到了TNFα和IL-1β,并且在Northern印迹上看到了这两种细胞因子的转录本。在未感染和慢性感染的细胞之间,未观察到这两种细胞因子产生的显著差异。然而,急性HIV感染的细胞表现出与成熟相一致的表型变化以及TNFα和IL-1β mRNA产生增加,并且与慢性感染或未感染的细胞相比,释放出显著更高水平的TNFα和IL-1β。此外,LPS刺激HIV感染的细胞会增加病毒产生。这些结果表明,HIV感染的单核细胞可能会在体内可能存在的刺激下产生增加量的TNFα和IL-1β。