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艾滋病逆转录病毒诱导的细胞病理学:巨细胞形成与CD4抗原的参与。

AIDS retrovirus induced cytopathology: giant cell formation and involvement of CD4 antigen.

作者信息

Lifson J D, Reyes G R, McGrath M S, Stein B S, Engleman E G

出版信息

Science. 1986 May 30;232(4754):1123-7. doi: 10.1126/science.3010463.

Abstract

The formation of multinucleated giant cells with progression to cell death is a characteristic manifestation of the cytopathology induced by the AIDS retrovirus in infected T lymphoid cells. The mechanism of giant cell formation was studied in the CD4 (T4/Leu 3) positive T cell lines JM (Jurkat) and VB and in variants of these lines that are negative for cell surface CD4 antigen. By means of a two-color fluorescent labeling technique, multinucleated giant cells in infected cultures were shown to form through cell fusion. Antibody to CD4 specifically inhibited fusion, and uninfected CD4 negative cells, in contrast to uninfected CD4 positive cells, did not undergo fusion with infected cells, suggesting a direct role for the CD4 antigen in the process of syncytium formation. These results suggest that, in vivo, cell fusion involving the CD4 molecule may represent a mechanism whereby uninfected cells can be incorporated into AIDS virus infected syncytia. Because the giant cells die soon after they are formed, this process may contribute to the depletion of helper/inducer T cells characteristically observed in AIDS.

摘要

多核巨细胞的形成并进展至细胞死亡是艾滋病逆转录病毒感染T淋巴细胞后诱导的细胞病理学特征性表现。在CD4(T4/Leu 3)阳性T细胞系JM(Jurkat)和VB以及这些细胞系中细胞表面CD4抗原呈阴性的变体中研究了巨细胞形成的机制。通过双色荧光标记技术,显示感染培养物中的多核巨细胞通过细胞融合形成。抗CD4抗体特异性抑制融合,与未感染的CD4阳性细胞相比,未感染的CD4阴性细胞不与感染细胞融合,提示CD4抗原在合胞体形成过程中起直接作用。这些结果表明,在体内,涉及CD4分子的细胞融合可能是一种机制,通过该机制未感染的细胞可被纳入艾滋病病毒感染的合胞体。由于巨细胞在形成后不久就死亡,这一过程可能导致艾滋病中特征性观察到的辅助/诱导性T细胞耗竭。

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