Analyzing the molecular foundations of commensalism in the mouse intestine
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Hooper, LV
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机构:Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
Hooper, LV
Falk, PG
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机构:Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
Falk, PG
Gordon, JI
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Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
Gordon, JI
[1
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机构:
[1] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[2] ASTRAZeneca, Dept Gastrointestinal Pharmacol, S-43183 Molndal, Sweden
We maintain complex societies of nonpathogenic microbes on our mucosal surfaces. Although the stability of this flora is important for human health, very little is known about how its constituents communicate with us to forge stable and mutually advantageous relationships. The vast majority of these indigenous microbes reside in the intestine. Recent studies of a gut commensal, Bacteroides thetaiotaomicron, has revealed a novel signaling pathway that allows the microbe and host to actively collaborate to produce a nutrient foundation that can be used by this bacterium. This pathway illustrates the type of dynamic molecular interactions that help define commensal relationships.