Regeneration of fat cells from myofibroblasts during wound healing.
Maksim V PlikusChristian F Guerrero-JuarezMayumi ItoYun Rose LiPriya H DedhiaYing ZhengMengle ShaoDenise L GayRaul RamosTsai-Ching HsiJi Won OhXiaojie WangAmanda RamirezSara E KonopelskiArijh ElzeinAnne WangRarinthip June SupapannachartHye-Lim LeeChae Ho LimArben NaceAmy GuoElsa TreffeisenThomas AndlRicardo N RamirezRabi MuradStefan OffermannsDaniel MetzgerPierre ChambonAlan D WidgerowTai-Lan TuanAli MortazaviRana K GuptaBruce A HamiltonSarah E MillarPatrick SealeWarren S PearMitchell A LazarGeorge CotsarelisPublished in: Science (New York, N.Y.) (2017)
Although regeneration through the reprogramming of one cell lineage to another occurs in fish and amphibians, it has not been observed in mammals. We discovered in the mouse that during wound healing, adipocytes regenerate from myofibroblasts, a cell type thought to be differentiated and nonadipogenic. Myofibroblast reprogramming required neogenic hair follicles, which triggered bone morphogenetic protein (BMP) signaling and then activation of adipocyte transcription factors expressed during development. Overexpression of the BMP antagonist Noggin in hair follicles or deletion of the BMP receptor in myofibroblasts prevented adipocyte formation. Adipocytes formed from human keloid fibroblasts either when treated with BMP or when placed with human hair follicles in vitro. Thus, we identify the myofibroblast as a plastic cell type that may be manipulated to treat scars in humans.
Keyphrases
- wound healing
- adipose tissue
- mesenchymal stem cells
- endothelial cells
- stem cells
- bone regeneration
- transcription factor
- insulin resistance
- fatty acid
- single cell
- induced pluripotent stem cells
- transforming growth factor
- pluripotent stem cells
- cell proliferation
- cell therapy
- metabolic syndrome
- high fat diet induced
- skeletal muscle
- extracellular matrix
- epithelial mesenchymal transition
- binding protein