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CCR5、CXCR4和CD4在人类巨噬细胞和T细胞的微绒毛上聚集并紧密相邻。

CCR5, CXCR4, and CD4 are clustered and closely apposed on microvilli of human macrophages and T cells.

作者信息

Singer I I, Scott S, Kawka D W, Chin J, Daugherty B L, DeMartino J A, DiSalvo J, Gould S L, Lineberger J E, Malkowitz L, Miller M D, Mitnaul L, Siciliano S J, Staruch M J, Williams H R, Zweerink H J, Springer M S

机构信息

Department of Immunology and Rheumotology, Merck Research Laboratories, Rahway, New Jersey 07065, USA.

出版信息

J Virol. 2001 Apr;75(8):3779-90. doi: 10.1128/JVI.75.8.3779-3790.2001.

Abstract

The chemokine receptors CCR5 and CXCR4 act synergistically with CD4 in an ordered multistep mechanism to allow the binding and entry of human immunodeficiency virus type 1 (HIV-1). The efficiency of such a coordinated mechanism depends on the spatial distribution of the participating molecules on the cell surface. Immunoelectron microscopy was performed to address the subcellular localization of the chemokine receptors and CD4 at high resolution. Cells were fixed, cryoprocessed, and frozen; 80-nm cryosections were double labeled with combinations of CCR5, CXCR4, and CD4 antibodies and then stained with immunogold. Surprisingly, CCR5, CXCR4, and CD4 were found predominantly on microvilli and appeared to form homogeneous microclusters in all cell types examined, including macrophages and T cells. Further, while mixed microclusters were not observed, homogeneous microclusters of CD4 and the chemokine receptors were frequently separated by distances less than the diameter of an HIV-1 virion. Such distributions are likely to facilitate cooperative interactions with HIV-1 during virus adsorption to and penetration of human leukocytes and have significant implications for development of therapeutically useful inhibitors of the entry process. Although the mechanism underlying clustering is not understood, clusters were observed in small trans-Golgi vesicles, implying that they were organized shortly after synthesis and well before insertion into the cellular membrane. Chemokine receptors normally act as sensors, detecting concentration gradients of their ligands and thus providing directional information for cellular migration during both normal homeostasis and inflammatory responses. Localization of these sensors on the microvilli should enable more precise monitoring of their environment, improving efficiency of the chemotactic process. Moreover, since selectins, some integrins, and actin are also located on or in the microvillus, this organelle has many of the major elements required for chemotaxis.

摘要

趋化因子受体CCR5和CXCR4与CD4协同作用,通过有序的多步骤机制,实现人类免疫缺陷病毒1型(HIV-1)的结合与进入。这种协同机制的效率取决于参与分子在细胞表面的空间分布。为了高分辨率地研究趋化因子受体和CD4的亚细胞定位,进行了免疫电子显微镜检查。细胞经固定、冷冻处理后冷冻保存;用CCR5、CXCR4和CD4抗体组合对80纳米的冷冻切片进行双重标记,然后用免疫金染色。令人惊讶的是,CCR5、CXCR4和CD4主要存在于微绒毛上,并且在所有检测的细胞类型(包括巨噬细胞和T细胞)中似乎都形成了均匀的微簇。此外,虽然未观察到混合微簇,但CD4和趋化因子受体的均匀微簇常常被小于HIV-1病毒粒子直径的距离隔开。这种分布可能有助于在病毒吸附和穿透人类白细胞过程中与HIV-1进行协同相互作用,并且对开发有效的进入过程治疗抑制剂具有重要意义。虽然聚集的潜在机制尚不清楚,但在小的反式高尔基体囊泡中观察到了微簇,这意味着它们在合成后不久且在插入细胞膜之前就已形成。趋化因子受体通常作为传感器,检测其配体的浓度梯度,从而在正常稳态和炎症反应期间为细胞迁移提供方向信息。这些传感器在微绒毛上的定位应能更精确地监测其周围环境,提高趋化过程的效率。此外,由于选择素、一些整合素和肌动蛋白也位于微绒毛上或微绒毛内,这个细胞器具备趋化作用所需的许多主要成分。

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