Abstract |
Evidence is accumulating to suggest that our indigenous microbial communities (microbiota) may have a role in modulating allergic and immune disorders of the skin. To examine the link between the microbiota and atopic dermatitis (AD), we examined a mouse model of defective cutaneous barrier function with an AD-like disease due to loss of Notch signaling. Comparisons of conventionally raised and germ-free (GF) mice revealed a similar degree of allergic skin inflammation, systemic atopy, and airway hypersensitivity. GF mutant animals expressed significantly higher levels of thymic stromal lymphopoietin, a major proinflammatory cytokine released by skin with defective barrier function, resulting in a more severe B- lymphoproliferative disorder that persisted into adulthood. These findings suggest a role for the microbiota in ameliorating stress signals released by keratinocytes in response to perturbation in cutaneous barrier function.
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Authors | Laura J Yockey, Shadmehr Demehri, Mustafa Turkoz, Ahu Turkoz, Philip P Ahern, Omar Jassim, Sindhu Manivasagam, John F Kearney, Jeffrey I Gordon, Raphael Kopan |
Journal | The Journal of investigative dermatology
(J Invest Dermatol)
Vol. 133
Issue 12
Pg. 2714-2721
(Dec 2013)
ISSN: 1523-1747 [Electronic] United States |
PMID | 23698100
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cytokines
- Immunoglobulin J Recombination Signal Sequence-Binding Protein
- Rbpj protein, mouse
- Immunoglobulin E
- Thymic Stromal Lymphopoietin
- TSLP protein, mouse
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Topics |
- Alleles
- Animals
- Cytokines
(metabolism)
- Female
- Gene Expression Regulation
- Genotype
- Hypersensitivity
(metabolism)
- Immunoglobulin E
(blood)
- Immunoglobulin J Recombination Signal Sequence-Binding Protein
(genetics)
- Inflammation
(metabolism)
- Keratinocytes
(cytology)
- Male
- Mice
- Mice, Knockout
- Microbiota
- Skin
(immunology, microbiology)
- Thymic Stromal Lymphopoietin
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