AI Article Synopsis

  • The skin serves as a vital barrier against dehydration and external threats, with keratinocytes (KCs) playing a key role in maintaining this barrier through Na ion transport.
  • In experiments with cultured KCs from adult mice, the absence of NFAT5 led to increased secretion of matrix proteinases like Mmp3 and Klk7, signaling NFAT5's regulatory role.
  • NFAT5 is crucial in controlling these proteinases to ensure skin integrity and developmental changes from embryos to adults, particularly by managing the delicate balance of protein expression in different stages of development.

Article Abstract

The skin protects the human body against dehydration and harmful challenges. Keratinocytes (KCs) are the most abundant epidermal cells, and it is anticipated that KC-mediated transport of Na ions creates a physiological barrier of high osmolality against the external environment. Here, we studied the role of NFAT5, a transcription factor whose activity is controlled by osmotic stress in KCs. Cultured KCs from adult mice were found to secrete more than 300 proteins, and upon NFAT5 ablation, the secretion of several matrix proteinases, including metalloproteinase-3 (Mmp3) and kallikrein-related peptidase 7 (Klk7), was markedly enhanced. An increase in Mmp3 and Klk7 RNA levels was also detected in transcriptomes of KCs, along with increases of numerous members of the 'Epidermal Differentiation Complex' (EDC), such as small proline-rich (Sprr) and S100 proteins. NFAT5 and Mmp3 as well as NFAT5 and Klk7 are co-expressed in the basal KCs of fetal and adult epidermis but not in basal KCs of newborn (NB) mice. The poor NFAT5 expression in NB KCs is correlated with a strong increase in Mmp3 and Klk7 expression in KCs of NB mice. These data suggests that, along with the fragile epidermis of adult mice, NFAT5 keeps in check the expression of matrix proteases in epidermis. The NFAT5-mediated control of matrix proteases in epidermis contributes to the manifold changes in skin development in embryos before and during birth, and to the integrity of epidermis in adults.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696207PMC
http://dx.doi.org/10.3389/fimmu.2021.780727DOI Listing

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