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脂肪细胞在暴露于HIV-1时脂联素的调节。

Regulation of adiponectin in adipocytes upon exposure to HIV-1.

作者信息

Sankalé J-L G, Tong Q, Hadigan C M, Tan G, Grinspoon S K, Kanki P J, Hotamisligil G S

机构信息

Department of Immunology & Infectious Diseases and Harvard AIDS Institute, Harvard School of Public Health, Boston, MA, USA.

出版信息

HIV Med. 2006 May;7(4):268-74. doi: 10.1111/j.1468-1293.2006.00372.x.

Abstract

OBJECTIVES

Adipose dysregulation, dyslipidemia, and insulin resistance are hallmarks of HIV-related lipodystrophy. The precise mechanisms behind these disturbances are unknown. In HIV-infected patients, we previously demonstrated a strong relationship between lipodystrophy and levels of adiponectin, an adipose peptide implicated in regulation of glucose and lipid metabolisms. In this study we investigated the effect of HIV on adipocytes, to determine whether HIV can directly infect adipocytes and/or alter the regulation and secretion of the adipocyte-derived hormone adiponectin.

METHODS

Human subcutaneous preadipocytes and adipocytes were exposed to HIV-1 under various conditions. Adiponectin was measured in supernatants and cell lysates.

RESULTS

Although adipocytes expressed CD4, the major HIV receptor, they could not be infected in vitro. However, exposure to HIV dramatically increased the secretion of adiponectin from human adipocytes, in the absence of infection. This was exacerbated with sustained exposure to HIV in a transwell assay. Further, human peripheral mononuclear cells also produced adiponectin, but this was largely dependent upon T-cell activation.

CONCLUSIONS

We propose that the stimulation of adiponectin production by HIV can perturb adiponectin regulation, leading to substantially decreased levels upon viral suppression by antiretroviral therapy. These data suggest a potential molecular mechanism of adiponectin regulation in HIV-infected patients.

摘要

目的

脂肪代谢失调、血脂异常和胰岛素抵抗是HIV相关脂肪代谢障碍的特征。这些紊乱背后的确切机制尚不清楚。在HIV感染患者中,我们之前证明了脂肪代谢障碍与脂联素水平之间存在密切关系,脂联素是一种参与调节葡萄糖和脂质代谢的脂肪肽。在本研究中,我们调查了HIV对脂肪细胞的影响,以确定HIV是否能直接感染脂肪细胞和/或改变脂肪细胞衍生激素脂联素的调节和分泌。

方法

在各种条件下,将人皮下前脂肪细胞和脂肪细胞暴露于HIV-1。检测上清液和细胞裂解物中的脂联素。

结果

尽管脂肪细胞表达主要的HIV受体CD4,但它们在体外不能被感染。然而,在未发生感染的情况下,暴露于HIV会显著增加人脂肪细胞脂联素的分泌。在transwell试验中,持续暴露于HIV会加剧这种情况。此外,人外周血单个核细胞也产生脂联素,但这很大程度上依赖于T细胞活化。

结论

我们提出,HIV对脂联素产生的刺激会扰乱脂联素的调节,导致在抗逆转录病毒疗法抑制病毒后脂联素水平大幅下降。这些数据提示了HIV感染患者中脂联素调节的潜在分子机制。

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