首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Human immunodeficiency virus-1 infection of macrophages in vitro neither induces tumor necrosis factor (TNF)/cachectin gene expression nor alters TNF/cachectin induction by lipopolysaccharide.
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Human immunodeficiency virus-1 infection of macrophages in vitro neither induces tumor necrosis factor (TNF)/cachectin gene expression nor alters TNF/cachectin induction by lipopolysaccharide.

机译:人巨噬细胞的人类免疫缺陷病毒1感染在体外既不诱导肿瘤坏死因子(TNF)/ cachectin基因表达也不改变脂多糖对TNF / cachectin的诱导。

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摘要

The synthesis of tumor necrosis factor (TNF)/cachectin was assessed in primary monocyte-derived macrophage (MDM) cultures after in vitro infection with a macrophage-tropic strain of HIV-1 (HTLV-IIIBa-L/85). Productive and cytopathic infections in MDM cultures were established using a high multiplicity of infection (m.o.i. = 3) under conditions that minimized endotoxin contamination. Culture supernatants were tested for TNF/cachectin activity by L929 cell cytotoxicity assay, and TNF/cachectin mRNA was assessed by a sensitive PCR amplification technique that could detect between 1 and 10 cells fully activated for TNF/cachectin expression. Unstimulated MDM cultures produced no detectable levels of TNF/cachectin activity or mRNA, consistent with previous demonstrations that production of this cytokine by macrophages is an inducible and not a constitutive event. HIV-1 infection failed to induce detectable TNF/cachectin activity or mRNA in these unstimulated cultures. In addition, the responsiveness of macrophages to lipopolysaccharide (LPS) induction of TNF/cachectin production was assessed in dose-response and kinetic experiments. No differences between infected and uninfected cultures were discernable. These results demonstrate that productive and cytopathic infection with a macrophage-tropic strain of HIV-1 does not alter the regulation of TNF/cachectin expression in macrophages.
机译:在感染了巨噬细胞嗜性HIV-1(HTLV-IIIBa-L / 85)后,在原代单核细胞衍生巨噬细胞(MDM)培养物中评估了肿瘤坏死因子(TNF)/ cachectin的合成。在使内毒素污染最小化的条件下,使用高度多重感染(m.o.i. = 3)来建立MDM培养物中的生产性感染和细胞病变感染。通过L929细胞细胞毒性测定法测试培养上清液的TNF / Cachectin活性,并通过灵敏的PCR扩增技术评估TNF / Cachectin mRNA,该技术可以检测到1至10个完全激活的TNF / Cachectin表达细胞。未经刺激的MDM培养物未产生可检测水平的TNF / Cachectin活性或mRNA,这与以前的证明一致,即巨噬细胞产生这种细胞因子是可诱导的而不是组成性事件。在这些未经刺激的培养物中,HIV-1感染未能诱导出可检测的TNF / Cachectin活性或mRNA。此外,在剂量反应和动力学实验中评估了巨噬细胞对脂多糖(LPS)诱导的TNF / Cachectin产生的反应。感染和未感染的培养物之间没有区别。这些结果表明,HIV-1的巨噬细胞嗜性株的生产性和细胞性感染不会改变巨噬细胞中TNF / cachectin表达的调节。

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