Gruber M F, Webb D S, Gerrard T L, Mostowski H S, Vujcic L, Golding H
Division of Cytokine Biology and Virology, Food and Drug Administration, National Institutes of Health, Bethesda, MD 20892.
AIDS Res Hum Retroviruses. 1991 Jan;7(1):45-53. doi: 10.1089/aid.1991.7.45.
The role of the adhesion molecules intercellular adhesion molecule-1 (ICAM-1) and LFA-1 in human immunodeficiency virus type 1 (HIV-1)-induced cell fusion was investigated in subclones of a T-cell leukemic cell line (CEM) with differing abilities to form syncytia. Addition of monoclonal antibodies 84H10 directed against ICAM-1 and MHM23 directed against the common beta subunit of LFA-1 (CD18) resulted in greater than 50% suppression of syncytia formation in cultures of these clones infected with cell-free virus. Two subclones, 2G5-144-84 and 2G5-1, were deficient in their ability to form syncytia and expressed reduced amounts of LFA-1 compared with the parental line. The expression of ICAM-1 but not LFA-1 was upregulated on the clones following treatment with interferon-gamma (IFN gamma); however, this did not overcome the delay in syncytia formation observed in these cells. The syncytia-positive subclones 1B11-39 and 17D-9 expressed high levels of LFA-1. Basal expression of ICAM-1 was upregulated on these cells by treatment with tumor necrosis factor-alpha (TNF alpha), which also accelerated and enhanced syncytia formation. However, anti-ICAM-1 and anti-LFA-1 (CD18) antibodies did not reverse the TNF alpha-induced enhancement of syncytia formation of HIV-1-infected clones 1B11-39 and 17D-9. Under conditions of low viral expression, adhesion molecules may contribute to syncytia formation if adequate levels of both receptor and ligand in the ICAM-1/LFA-1 complex are expressed.(ABSTRACT TRUNCATED AT 250 WORDS)
在具有不同形成多核巨细胞能力的T细胞白血病细胞系(CEM)亚克隆中,研究了黏附分子细胞间黏附分子-1(ICAM-1)和淋巴细胞功能相关抗原-1(LFA-1)在1型人类免疫缺陷病毒(HIV-1)诱导的细胞融合中的作用。添加针对ICAM-1的单克隆抗体84H10和针对LFA-1共同β亚基(CD18)的MHM23,可使这些感染无细胞病毒的克隆培养物中的多核巨细胞形成受到超过50%的抑制。两个亚克隆2G5-144-84和2G5-1形成多核巨细胞的能力不足,与亲代细胞系相比,其LFA-1表达量降低。用干扰素-γ(IFNγ)处理后,这些克隆上ICAM-1的表达上调,但LFA-1未上调;然而,这并未克服在这些细胞中观察到的多核巨细胞形成延迟。多核巨细胞阳性亚克隆1B11-39和17D-9表达高水平的LFA-1。用肿瘤坏死因子-α(TNFα)处理可使这些细胞上ICAM-1的基础表达上调,这也加速并增强了多核巨细胞的形成。然而,抗ICAM-1和抗LFA-1(CD18)抗体并未逆转TNFα诱导的HIV-1感染克隆1B11-39和17D-9多核巨细胞形成增强。在低病毒表达条件下,如果ICAM-1/LFA-1复合物中的受体和配体都表达足够水平,则黏附分子可能有助于多核巨细胞的形成。(摘要截短于250字)