Occludin, caveolin‐1, and Alix form a multi‐protein complex and regulate HIV‐1 infection of brain pericytes. Issue 12 (14th October 2020)

• Record Type: Journal Article
• Authors: Torices, Silvia; Roberts, Samantha A.; Park, Minseon; Malhotra, Arun; Toborek, Michal
• Is Part Of: FASEB journal. Volume 34:Issue 12(2020)
• Page Start: 16319
• Page End: 16332
• Publication Date: 2020-10-14
• Subjects: Alix -- blood‐brain barrier -- caveolin‐1 -- HIV‐1 -- pericytes; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.202001562R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: HIV‐1 enters the brain by altering properties of the blood‐brain barrier (BBB). Recent evidence indicates that among cells of the BBB, pericytes are prone to HIV‐1 infection. Occludin (ocln) and caveolin‐1 (cav‐1) are critical determinants of BBB integrity that can regulate barrier properties of the BBB in response to HIV‐1 infection. Additionally, Alix is an early acting endosomal factor involved in HIV‐1 budding from the cells. The aim of the present study was to evaluate the role of cav‐1, ocln, and Alix in HIV‐1 infection of brain pericytes. Our results indicated that cav‐1, ocln, and Alix form a multi‐protein complex in which they cross‐regulate each other's expression. Importantly, the stability of this complex was affected by HIV‐1 infection. Modifications of the complex resulted in diminished HIV‐1 infection and alterations of the cytokine profile produced by brain pericytes. These results identify a novel mechanism involved in HIV‐1 infection contributing to a better understanding of the HIV‐1 pathology and the associated neuroinflammatory responses.