共 61 条
Restriction of Legionella pneumophila growth in macrophages requires the concerted action of cytokine and Naip5/Ipaf signalling pathways
被引:111
作者:

Coers, Joern
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机构:
Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA

Vance, Russell E.
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机构: Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA

Fontana, Mary F.
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机构: Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA

Dietrich, William F.
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机构: Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[3] Novartis Inst BioMed Res, Mouse Genet & Toxicol Models Dis Ctr, Cambridge, MA 02139 USA
关键词:
D O I:
10.1111/j.1462-5822.2007.00963.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Macrophages from the C57BL/6 (B6) mouse strain restrict intracellular growth of Legionella pneumophila, whereas A/J macrophages are highly permissive. The mechanism by which B6 macrophages restrict Legionella growth remains poorly understood, but is known to require the cytosolic microbe sensors Naip5 (Birc1e) and Ipaf. We hypothesized that Naip5 and Ipaf may act in partnership with other antimicrobial signalling pathways in macrophages. Indeed, we found that macrophages lacking either tumour necrosis factor (TNF)-alpha or type I interferon (IFN) signalling are permissive for growth of L. pneumophila, even in the presence of functional Naip5 and Ipaf alleles. Similarly, macrophages lacking Naip5 and/or Ipaf signalling were permissive even though we found that Naip5 or Ipaf were not required for induction of TNF-alpha and type I IFN. Therefore, our data suggest that the mechanism by which B6 macrophages restrict intracellular replication of L. pneumophila is more complex than previously appreciated, and involves the concerted action of cytokine and intracellular microbe sensor signalling pathways.
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页码:2344 / 2357
页数:14
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