Bcl-3, induced by Tax and HTLV-1, inhibits NF-κB activation and promotes autophagy

Cell Signal. 2013 Dec;25(12):2797-804. doi: 10.1016/j.cellsig.2013.09.010. Epub 2013 Sep 14.

Abstract

The human T cell leukemia virus type 1 (HTLV-1) is a complex human retrovirus that causes an aggressive leukemia known as adult T cell leukemia (ATL). The HTLV-1-encoded oncoprotein Tax induces persistent activation of the nuclear factor-κB (NF-κB) pathway, which is perceived as the primary cause of ATL. Bcl-3, a member of the NF-κB inhibitor (IκB) family, is highly expressed in many HTLV-1-infected T cell lines and ATL cells. However, the role of Bcl-3 in Tax-induced NF-κB activation has not been fully elucidated. Here, we show that Tax induces Bcl-3 expression, which in turn negatively regulates the Tax-induced NF-κB activation. Interestingly, both Bcl-3 up-regulation and NF-κB inhibition promote the autophagy process in HTLV-1-infected cells. Consistent with this, over-expression of Bcl-3 also results in enhancement of rapamycin-, pifithrin-α- or starvation-induced autophagy in control cells. Together, these data demonstrate that Bcl-3 acts as a negative regulator of NF-κB activation and promotes autophagy in HTLV-1-infected cells.

Keywords: Autophagy; Bcl-3; HTLV-1; NF-κB activation; Tax.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy
  • B-Cell Lymphoma 3 Protein
  • Gene Expression Regulation, Neoplastic
  • Gene Products, tax / immunology*
  • HTLV-I Infections / genetics
  • HTLV-I Infections / immunology*
  • HTLV-I Infections / virology
  • HeLa Cells
  • Human T-lymphotropic virus 1 / immunology*
  • Humans
  • Jurkat Cells
  • Lymphoma, T-Cell / genetics
  • Lymphoma, T-Cell / immunology*
  • Lymphoma, T-Cell / virology
  • NF-kappa B / immunology*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / immunology*
  • Signal Transduction
  • T-Lymphocytes / immunology
  • T-Lymphocytes / virology*
  • Transcription Factors / genetics
  • Transcription Factors / immunology*
  • Transcriptional Activation

Substances

  • B-Cell Lymphoma 3 Protein
  • BCL3 protein, human
  • Gene Products, tax
  • NF-kappa B
  • Proto-Oncogene Proteins
  • Transcription Factors