Matrix protein mediated shutdown of host cell metabolism limits vesicular stomatitis virus-induced interferon-alpha responses to plasmacytoid dendritic cells

Immunobiology. 2007;212(9-10):887-94. doi: 10.1016/j.imbio.2007.09.003. Epub 2007 Nov 9.

Abstract

Upon infection with many different viruses, plasmacytoid dendritic cells (pDC) produce large amounts of type I interferon (IFN-alpha/beta). To address why upon vesicular stomatitis virus (VSV) infection pDC, but not conventional myeloid DC (mDC), are induced to produce IFN-alpha, pDC and mDC were differentiated from bone marrow cells (BM-DC). Upon VSV infection BM-pDC produced IFN-alpha, whereas BM-mDC did not. Notably, upon infection with VSV-M2, a VSV variant expressing a M51R mutant matrix (M) protein that showed a reduced sequestration of host cell metabolism, BM-pDC and BM-mDC mounted massive IFN-alpha responses. Both DC subsets showed comparable RNA levels of retinoic acid inducible gene-I (RIG-I) and Toll-like receptor (TLR) 7 and were able to respond upon triggering with double-stranded RNA (dsRNA) or single-stranded RNA (ssRNA) analogs. Moreover, upon VSV-M2 infection IFN-alpha production by both DC subsets was largely dependent on viral replication. Interestingly, upon virus infection BM-pDC, but not BM-mDC, up-regulated mRNA levels of nuclear export factors Nup96/98, probably reflecting cellular mechanisms to circumvent viral escape strategies. Collectively, these results indicated that cell types induced to produce IFN-alpha upon viral infection are not primarily defined by cellular receptor configurations but rather by complex virus/host cell interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cells, Cultured
  • Dendritic Cells / immunology*
  • Dendritic Cells / virology*
  • Interferon-alpha / biosynthesis*
  • Interferon-alpha / blood
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Nuclear Pore Complex Proteins / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Cell Surface
  • Rhabdoviridae Infections / immunology*
  • Rhabdoviridae Infections / virology
  • Toll-Like Receptor 7 / genetics
  • Toll-Like Receptor 7 / metabolism
  • Vesicular stomatitis Indiana virus / immunology*
  • Vesicular stomatitis Indiana virus / physiology
  • Viral Matrix Proteins / physiology*
  • Virus Replication

Substances

  • Interferon-alpha
  • M protein, Vesicular stomatitis virus
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Nuclear Pore Complex Proteins
  • RNA, Messenger
  • Receptors, Cell Surface
  • Robo3 protein, mouse
  • Toll-Like Receptor 7
  • Viral Matrix Proteins
  • nuclear pore complex protein 96
  • nuclear pore complex protein 98