AI Article Synopsis

  • Melanocyte stem cells (McSCs) and mouse models of hair graying are utilized to study stem cell self-renewal and tissue maintenance.
  • Researchers found that a specific genetic variant (heterozygosity for the Mitf gene) increases McSC differentiation and contributes to hair graying in susceptible mice.
  • The study reveals a new role for the MITF protein in regulating immune gene expression, and highlights how immune system dysregulation may affect pigmentation, which could relate to conditions like vitiligo.

Article Abstract

Melanocyte stem cells (McSCs) and mouse models of hair graying serve as useful systems to uncover mechanisms involved in stem cell self-renewal and the maintenance of regenerating tissues. Interested in assessing genetic variants that influence McSC maintenance, we found previously that heterozygosity for the melanogenesis associated transcription factor, Mitf, exacerbates McSC differentiation and hair graying in mice that are predisposed for this phenotype. Based on transcriptome and molecular analyses of Mitfmi-vga9/+ mice, we report a novel role for MITF in the regulation of systemic innate immune gene expression. We also demonstrate that the viral mimic poly(I:C) is sufficient to expose genetic susceptibility to hair graying. These observations point to a critical suppressor of innate immunity, the consequences of innate immune dysregulation on pigmentation, both of which may have implications in the autoimmune, depigmenting disease, vitiligo.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933715PMC
http://dx.doi.org/10.1371/journal.pbio.2003648DOI Listing

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