4.6 Article

Tight junction regulation by morphine and HIV-1 tat modulates blood-brain barrier permeability

期刊

JOURNAL OF CLINICAL IMMUNOLOGY
卷 28, 期 5, 页码 528-541

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10875-008-9208-1

关键词

morphine; neuropathogenesis; HIV-1; HIV-1 associated dementia; blood-brain barrier; tight junctions; drug abuse

资金

  1. Margaret Duffy
  2. Robert Cameron Troup Memorial Fund of Kaleida Health
  3. Kaleida Health Foundation

向作者/读者索取更多资源

Human immunodeficiency virus (HIV)-1 patients who abuse opiates are at a greater risk of developing neurological complications of AIDS. Alterations in blood-brain barrier (BBB) integrity are associated with cytoskeletal disorganization and disruption of tight junction (TJ) integrity. We hypothesize that opiates in combination with HIV-1 viral proteins can modulate TJ expression in primary brain microvascular endothelial cells (BMVEC), thereby compromising BBB integrity and exacerbating HIV-1 neuropathogenesis. We investigated the effect of morphine and/or tat on the expression of TJ proteins ZO-1, JAM-2, Occludin and P-glycoprotein and the functional effects of TJ modulation in BMVEC. Morphine and/or tat, via the activation of pro-inflammatory cytokines, intracellular Ca2+ release, and activation of myosin light chain kinase, modulated TJ expression resulting in decreased transendothelial electric resistance and enhanced transendothelial migration across the BBB. These studies may lead to the development of novel anti-HIV-1 therapeutics that target specific TJ proteins, thus preventing TJ disruption in opiate using HIV-1 patients.

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