Human immunodeficiency virus type-1 infection inhibits autophagy.

Dejiang Zhou, Stephen A Spector
Author Information
  1. Dejiang Zhou: Department of Pediatrics, Division of Infectious Diseases, University of California San Diego, La Jolla, California, 92093-0672, USA.

Abstract

OBJECTIVES: Human immunodeficiency virus type-1 (HIV-1) induces a series of alterations in the host cell that modify the intracellular environment in favor of viral replication, survival and spread. This research examined the impact of HIV-1 infection on autophagy in HIV-1 infected cells.
METHODS: Protein extracts of HIV-1 infected and control CD4+ T-lymphocytes and U937 cells were semi-quantified by western blot. The autophagy-related protein Beclin 1, a Bcl-2 associated protein, and the 16 kD microtubule-associated protein (MAP) light chain three (LC3) which is essential for autophagy were quantified and validated using the intracellular protein GAPDH as an internal standard. Beclin 1 mRNA was quantified by real-time reverse transcriptase-polymerase chain reaction. Autophagosomes were assessed by visualization under confocal microscopy following intracellular staining of the LC3 protein.
RESULTS: Following infection of human peripheral blood CD4+ T-cells or U937 cells with HIV-1 for 48 h, the autophagy protein Beclin 1 and LC3 II, which is essential for autophagy, were found to be markedly decreased. Beclin 1 mRNA expression was also reduced. Autophagosomes were reduced in HIV-1-infected cells. The reduction of autophagic protein expression and autophagosomes in HIV-1-infected cells could be overcome by amino acid starvation or rapamycin.
CONCLUSIONS: These data demonstrate that HIV-1 infection can down-regulate autophagy in infected cells during acute infection, and provide new insights into HIV-1-induced cell death and disease-related pathogenesis.

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Grants

  1. AI-68632/NIAID NIH HHS
  2. U01 AI068632/NIAID NIH HHS
  3. UM1 AI068632/NIAID NIH HHS
  4. U01 AI068632-03/NIAID NIH HHS
  5. R01 AI039004/NIAID NIH HHS
  6. P30 AI036214/NIAID NIH HHS
  7. AI-36214/NIAID NIH HHS
  8. AI-39004/NIAID NIH HHS

MeSH Term

Acute Disease
Amino Acids
Apoptosis Regulatory Proteins
Autophagy
Beclin-1
Biomarkers
CD4-Positive T-Lymphocytes
Cell Line
HIV Infections
HIV-1
Humans
Immunosuppressive Agents
Membrane Proteins
Microscopy, Confocal
Microtubule-Associated Proteins
RNA, Messenger
Reverse Transcriptase Polymerase Chain Reaction
Sirolimus
Virus Replication

Chemicals

Amino Acids
Apoptosis Regulatory Proteins
BECN1 protein, human
Beclin-1
Biomarkers
Immunosuppressive Agents
MAP1LC3A protein, human
Membrane Proteins
Microtubule-Associated Proteins
RNA, Messenger
Sirolimus

Word Cloud

Created with Highcharts 10.0.0proteinHIV-1autophagycellsinfectionBeclin1intracellularinfectedLC3Humanimmunodeficiencyvirustype-1cellCD4+U937chainessentialquantifiedmRNAAutophagosomesexpressionreducedHIV-1-infectedOBJECTIVES:inducesseriesalterationshostmodifyenvironmentfavorviralreplicationsurvivalspreadresearchexaminedimpactMETHODS:ProteinextractscontrolT-lymphocytessemi-quantifiedwesternblotautophagy-relatedBcl-2associated16kDmicrotubule-associatedMAPlightthreevalidatedusingGAPDHinternalstandardreal-timereversetranscriptase-polymerasereactionassessedvisualizationconfocalmicroscopyfollowingstainingRESULTS:FollowinghumanperipheralbloodT-cells48hIIfoundmarkedlydecreasedalsoreductionautophagicautophagosomesovercomeaminoacidstarvationrapamycinCONCLUSIONS:datademonstratecandown-regulateacuteprovidenewinsightsHIV-1-induceddeathdisease-relatedpathogenesisinhibits

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