Endolysosome iron restricts Tat-mediated HIV-1 LTR transactivation by increasing HIV-1 Tat oligomerization and β-catenin expression.

Deferoxamine (DFO) Endolysosomes HIV-1-associated neurocognitive disorder (HAND) Oligomerization People living with HIV-1 (PLWH) Tat-mediated HIV-1 LTR transactivation Transactivator of transcription (Tat)

Journal

Journal of neurovirology
ISSN: 1538-2443
Titre abrégé: J Neurovirol
Pays: United States
ID NLM: 9508123

Informations de publication

Date de publication:
10 2021
Historique:
received: 15 04 2021
accepted: 24 08 2021
revised: 06 08 2021
pubmed: 23 9 2021
medline: 17 3 2022
entrez: 22 9 2021
Statut: ppublish

Résumé

HIV-1 transactivator of transcription (Tat) protein is required for HIV-1 replication, and it has been implicated in the pathogenesis of HIV-1-associated neurocognitive disorder (HAND). HIV-1 Tat can enter cells via receptor-mediated endocytosis where it can reside in endolysosomes; upon its escape from these acidic organelles, HIV-1 Tat can enter the cytosol and nucleus where it activates the HIV-1 LTR promoter. Although it is known that HIV-1 replication is affected by the iron status of people living with HIV-1 (PLWH), very little is known about how iron affects HIV-1 Tat activation of the HIV-1 LTR promoter. Because HIV-1 proteins de-acidify endolysosomes and endolysosome de-acidification affects subcellular levels and actions of iron, we tested the hypothesis that the endolysosome pool of iron is sufficient to affect Tat-induced HIV-1 LTR transactivation. Ferric (Fe

Identifiants

pubmed: 34550543
doi: 10.1007/s13365-021-01016-5
pii: 10.1007/s13365-021-01016-5
pmc: PMC8602775
mid: NIHMS1749333
doi:

Substances chimiques

CTNNB1 protein, human 0
beta Catenin 0
tat Gene Products, Human Immunodeficiency Virus 0
Iron E1UOL152H7

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

755-773

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS065957
Pays : United States
Organisme : NIGMS NIH HHS
ID : U54 GM115458
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH119000
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH100972
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH105329
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032444
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM100329
Pays : United States

Informations de copyright

© 2021. Journal of NeuroVirology, Inc.

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Auteurs

Nabab Khan (N)

Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA.

Peter W Halcrow (PW)

Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA.

Leo K Lakpa (LK)

Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA.

Mohd Rehan (M)

King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

Xuesong Chen (X)

Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA.

Jonathan D Geiger (JD)

Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA. jonathan.geiger@und.edu.

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Classifications MeSH