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A Biphasic Innate Immune MAPK Response Discriminates Between the Yeast and Hyphal Forms of Candida Albicans in Epithelial Cells

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Publisher Cell Press
Date 2010 Sep 14
PMID 20833374
Citations 195
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Abstract

Discriminating between commensal and pathogenic states of opportunistic pathogens is critical for host mucosal defense and homeostasis. The opportunistic human fungal pathogen Candida albicans is also a constituent of the normal oral flora and grows either as yeasts or hyphae. We demonstrate that oral epithelial cells orchestrate an innate response to C. albicans via NF-κB and a biphasic MAPK response. Activation of NF-κB and the first MAPK phase, constituting c-Jun activation, is independent of morphology and due to fungal cell wall recognition. Activation of the second MAPK phase, constituting MKP1 and c-Fos activation, is dependent upon hypha formation and fungal burdens and correlates with proinflammatory responses. Such biphasic response may allow epithelial tissues to remain quiescent under low fungal burdens while responding specifically and strongly to damage-inducing hyphae when burdens increase. MAPK/MKP1/c-Fos activation may represent a "danger response" pathway that is critical for identifying and responding to the pathogenic switch of commensal microbes.

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References
1.
Wang X, Liu Y . Regulation of innate immune response by MAP kinase phosphatase-1. Cell Signal. 2007; 19(7):1372-82. PMC: 2203964. DOI: 10.1016/j.cellsig.2007.03.013. View

2.
Chi H, Flavell R . Acetylation of MKP-1 and the control of inflammation. Sci Signal. 2008; 1(41):pe44. PMC: 2613485. DOI: 10.1126/scisignal.141pe44. View

3.
Naglik J, Fostira F, Ruprai J, Staab J, Challacombe S, Sundstrom P . Candida albicans HWP1 gene expression and host antibody responses in colonization and disease. J Med Microbiol. 2006; 55(Pt 10):1323-1327. PMC: 3244616. DOI: 10.1099/jmm.0.46737-0. View

4.
Korting H, Hube B, Oberbauer S, Januschke E, Hamm G, Albrecht A . Reduced expression of the hyphal-independent Candida albicans proteinase genes SAP1 and SAP3 in the efg1 mutant is associated with attenuated virulence during infection of oral epithelium. J Med Microbiol. 2003; 52(Pt 8):623-632. DOI: 10.1099/jmm.0.05125-0. View

5.
Kinney C, Chandrasekharan U, Mavrakis L, DiCorleto P . VEGF and thrombin induce MKP-1 through distinct signaling pathways: role for MKP-1 in endothelial cell migration. Am J Physiol Cell Physiol. 2007; 294(1):C241-50. DOI: 10.1152/ajpcell.00187.2007. View