Rapamycin-induced modulation of HIV gene transcription attenuates progression of HIVAN

Partab Rai, Andrei Plagov, Dileep Kumar, Shresh Pathak, Kamesh R Ayasolla, Amrita K Chawla, Peter W Mathieson, Moin A Saleem, Mohammad Husain, Ashwani Malhotra, Pravin C Singhal

Research output: Contribution to journalArticle (Academic Journal)peer-review

16 Citations (Scopus)

Abstract

HIV-associated nephropathy (HIVAN) is the manifestation of HIV gene expression by kidney cells in the presence of specific host factors. Recently, rapamycin (sirolimus) has been demonstrated to modulate the progression of HIVAN. We hypothesized that rapamycin would modulate the progression of HIVAN by attenuating HIV gene expression. To test our hypothesis, three weeks old Tg26 mice (n=6) were administered either vehicle or rapamycin (5 mg/kg, every other day, intraperitoneal) for eight weeks. At the end of the experimental period, the kidneys were harvested. In in vitro studies, human podocytes were transduced with either HIV-1 (NL4-3) or empty vector (EV), followed by treatment with either vehicle or rapamycin. Total RNA and proteins were extracted from renal tissues/cellular lysates and HIV gene transcription/translation was measured by real time PCR and Western blotting studies. Renal histological slides were graded for glomerular sclerosis and tubular dilatation with microcyst formation. Rapamycin attenuated both glomerular and tubular lesions in Tg26 mice. Rapamycin decreased transcription of HIV genes both in renal tissues as well as in HIV-1 transduced podocytes. Our data strongly indicate that HIV-1 long terminal repeat-mediated transcriptional activity was targeted by rapamycin. Rapamycin enhanced podocyte NF-κB and CREB activities but then it decreased AP-1 binding activity. Since expression of HIV genes by kidney cells has been demonstrated to be the key factor in the development HIVAN, it appears that rapamycin-induced altered transcription of HIV genes might have partly contributed to its disease modulating effects.

Original languageEnglish
Pages (from-to)255-61
Number of pages7
JournalExperimental and Molecular Pathology
Volume94
Issue number1
DOIs
Publication statusPublished - Feb 2013

Keywords

  • AIDS-Associated Nephropathy
  • Animals
  • Cell Proliferation
  • Cells, Cultured
  • Cyclic AMP Response Element-Binding Protein
  • Disease Models, Animal
  • Disease Progression
  • HIV-1
  • Humans
  • Kidney
  • Kidney Glomerulus
  • Kidney Tubules
  • Mice
  • NF-kappa B
  • Podocytes
  • Sclerosis
  • Sirolimus
  • Transcription Factor AP-1
  • Transcription, Genetic

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