| Literature DB >> 31940497 |
Paola Cattaneo1, Debanjan Mukherjee2, Simone Spinozzi3, Lunfeng Zhang4, Veronica Larcher5, William B Stallcup6, Hiroshi Kataoka7, Ju Chen3, Stefanie Dimmeler8, Sylvia M Evans9, Nuno Guimarães-Camboa10.
Abstract
Despite decades of studies suggesting that the in vivo adipocyte progenitor resides within the vascular niche, the exact nature of this progenitor remains controversial because distinct studies have attributed adipogenic properties to multiple vascular cell types. Using Cre recombinases labeling distinct vascular lineages, we conduct parallel lineage tracing experiments to assess their degree of contribution to de novo adipogenesis. Although we detect occasional adipocytes that were lineage traced by endothelial or mural recombinases, these are rare events. On the other hand, platelet-derived growth factor receptor alpha (PDGFRα)-expressing adventitial or capsular fibroblasts make a significant contribution to adipocytes in all depots and experimental settings tested. Our data also suggest that fibroblasts transition to an intermediate beige adipocyte phenotype prior to differentiating to a mature white adipocyte. These observations, together with histological analyses revealing that adipose tissue fibroblasts express the mural cell marker PDGFRβ, harmonize a highly controversial field with implications for multiple human diseases, including the pandemic of obesity.Entities:
Keywords: adipogenesis; endothelium; fibroblasts; lineage tracing; mural cells; obesity; vascular wall
Mesh:
Year: 2020 PMID: 31940497 DOI: 10.1016/j.celrep.2019.12.046
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423