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Biology subjects

Haga, M.

Publications and source records attributed to Haga, M..

2 recordsLinked to original sources

The heterogeneity of dermal mesenchymal cells reproduced in skin equivalents regulate barrier function and elasticity.

The heterogeneity of dermal mesenchymal cells, including perivascular mesenchymal cells and papillary and reticular fibroblasts, plays critical roles in skin homeostasis. Herein, we present human skin equivalents (HSEs), in which pericytes, papillary fibroblasts, and reticular fibroblasts are spatially organized through autonomous three-cell interactions among epidermal keratinocytes, dermal fibroblasts, and vascular endothelial cells. The replication of dermal mesenchymal cell heterogeneity enhances skin functions, including epithelialization, epidermal barrier formation, and dermal elasticity, enabling in vitro evaluation of drug efficacy using methodologies that are identical to those used in human clinical studies. Furthermore, ascorbic acid-induced epidermal turnover and synthesis of well-aligned extracellular matrix via perivascular niche cells play crucial roles in improving skin barrier function and elasticity. Therefore, HSEs with heterogeneous dermal mesenchymal cells may improve our understanding of the mechanisms underlying skin homeostasis through cell-to-cell communication and serve as a model to animal experiments for developing precision medicine.

bioengineering↗

Positive and negative feedback regulation of the TGF-β1-SMAD4 axis explains two equilibrium states in human skin aging

Skin homeostasis during aging is critical not only for the appearance but also biological defense of the human body. In this study, we identified thrombospondin-1 (THBS1) and fibromodulin (FMOD) as positive and negative regulators, respectively, of the TGF-{beta}1-SMAD4 axis in human skin aging based on in vitro and in vivo omics analyses and mathematical modeling. Transcriptomic and epigenetic analyses of senescent dermal fibroblasts identified TGF-{beta}1 as the key upstream regulator. Bifurcation analysis identified a binary senescent/non-senescent switch, with THBS1 as the main controller. Sensitivity analysis of the TGF-{beta}1 signaling pathway indicated that THBS1 expression was sensitively regulated while FMOD was robustly regulated, suggesting that THBS1 is a controllable factor. Inhibition of SMAD4 complex formation was experimentally validated as a promising manner to control THBS1 production and senescence. This study demonstrates the potential of a data-driven mathematical approach in determining the mechanisms of skin aging. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=200 SRC="FIGDIR/small/546970v1_ufig1.gif" ALT="Figure 1"> View larger version (69K): org.highwire.dtl.DTLVardef@12b4f29org.highwire.dtl.DTLVardef@5a3e95org.highwire.dtl.DTLVardef@c2daa5org.highwire.dtl.DTLVardef@a09042_HPS_FORMAT_FIGEXP M_FIG C_FIG eTOC BlurbHaga, Iida and Okada revealed that the balance between FMOD and THBS1 determines the two equilibrium states of skin homeostasis and THBS1 is a controllable factor in skin aging HighlightsO_LIMulti-omics analysis identified TGF-{beta}1-SMAD4 as key regulators in human skin aging C_LIO_LITHBS1 and FMOD promoted and suppressed factors in skin aging, respectively C_LIO_LITHBS1 controlled the senescent and non-senescent states of the aging switch C_LIO_LISMAD4 is a potential target for inhibiting THBS1 expression and cell senescence C_LI

systems biology↗