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gp120存在于从HIV-1感染个体淋巴结制备的凋亡CD4细胞的质膜上:一项免疫电子显微镜研究。

gp120 is present on the plasma membrane of apoptotic CD4 cells prepared from lymph nodes of HIV-1-infected individuals: an immunoelectron microscopic study.

作者信息

Sunila I, Vaccarezza M, Pantaleo G, Fauci A S, Orenstein J M

机构信息

George Washington University Medical Center, Department of Pathology, Washington, DC 20037, USA.

出版信息

AIDS. 1997 Jan;11(1):27-32. doi: 10.1097/00002030-199701000-00005.

Abstract

OBJECTIVE

To study whether free gp120 can be detected on the plasma membranes of apoptotic CD4+ T lymphocytes in lymph nodes from HIV-positive patients.

METHODS

Lymph-node cell suspensions prepared from three HIV-positive patients were studied by pre-embedding, double-immunogold-labeling to identify cell type, determine cell morphology, and detect the presence of bound gp120 molecules. Cells were classified by their surface antigens as helper/inducer T lymphocytes (CD4+), cytotoxic/suppressor T lymphocytes (CD8+), B cells (CD20+), and total lymphocytes [CD45+, leukocyte common antigen (LCA)+].

RESULTS

gp120 colabelled with both apoptotic and normal CD4+ T lymphocytes and LCA+ cells, but not with either apoptotic or normal CD8+ T lymphocytes or B cells. gp120 was more often identified on apoptotic than on normal CD4+ T lymphocytes. The gp120 and CD45 label were often colocalized. HIV particles were not identified to be associated with or budding from either normal or apoptotic lymphocytes.

CONCLUSIONS

Free gp120 is found bound to CD4+ T cells in lymph nodes of HIV-infected individuals and potentially mark them for premature death by apoptosis.

摘要

目的

研究在HIV阳性患者淋巴结中,凋亡的CD4 + T淋巴细胞质膜上是否能检测到游离的gp120。

方法

对3例HIV阳性患者制备的淋巴结细胞悬液进行包埋前双重免疫金标记研究,以鉴定细胞类型、确定细胞形态并检测结合的gp120分子的存在。根据细胞表面抗原将细胞分类为辅助/诱导性T淋巴细胞(CD4 +)、细胞毒性/抑制性T淋巴细胞(CD8 +)、B细胞(CD20 +)和总淋巴细胞[CD45 +,白细胞共同抗原(LCA)+]。

结果

gp120与凋亡和正常的CD4 + T淋巴细胞以及LCA +细胞共标记,但不与凋亡或正常的CD8 + T淋巴细胞或B细胞共标记。在凋亡的CD4 + T淋巴细胞上比在正常的CD4 + T淋巴细胞上更常鉴定到gp120。gp120和CD45标记经常共定位。未发现HIV颗粒与正常或凋亡淋巴细胞相关或从其出芽。

结论

在HIV感染个体的淋巴结中发现游离的gp120与CD4 + T细胞结合,并可能通过凋亡标记它们过早死亡。

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