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Accession IconSRP166081

Age-related loss of innate immune antimicrobial function of dermal fat is mediated by TGFß

Organism Icon Mus musculus
Sample Icon 15 Downloadable Samples
Technology Badge IconNextSeq 500

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Description
Dermal fibroblasts (dFB) resist infection by locally differentiating into adipocytes and producing the antimicrobial peptide cathelicidin in response to S. aureus. We found that neonatal dFB were highly adipogenic whereas this adipogenic function was lost during adulthood. To better understand the molecular nature of the change in antimicrobial and adipogenic function of dFB, we profiled the transcriptomes of primary dFB isolated at different ages by RNA-seq. RNA-seq identified the pro-adipogenic to pro-fibrotic gene signature switch in dFB during aging, and identified TGF-beta as the top up-regulated pathway that was activated in 2M dFB compared to neonatal P1 dFB. Overall design: Examination of differentially expressed genes in cultured primary dermal fibroblasts/pre-adipocytes isolated from mouse skin with various ages.
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15
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