Mice lacking PLAP-1/asporin counteracts high fat diet-induced metabolic disorder and alveolar bone loss by controlling adipose tissue expansion

Sci Rep. 2021 Mar 2;11(1):4970. doi: 10.1038/s41598-021-84512-2.

Abstract

Adipose tissue fibrosis with chronic inflammation is a hallmark of obesity-related metabolic disorders, and the role of proteoglycans in developing adipose tissue fibrosis is of interest. Periodontal disease is associated with obesity; however, the underlying molecular mechanisms remain unclear. Here we investigated the roles of periodontal ligament associated protein-1 (PLAP-1)/asporin, a proteoglycan preferentially and highly expressed in the periodontal ligament, in obesity-related adipose tissue dysfunction and adipocyte differentiation. It was found that PLAP-1 is also highly expressed in white adipose tissues. Plap-1 knock-out mice counteracted obesity and alveolar bone resorption induced by a high-fat diet. Plap-1 knock-down in 3T3-L1 cells resulted in less lipid accumulation, and recombinant PLAP-1 enhanced lipid accumulation in 3T3-L1 cells. In addition, it was found that primary preadipocytes isolated from Plap-1 knock-out mice showed lesser lipid accumulation than the wild-type (WT) mice. Furthermore, the stromal vascular fraction of Plap-1 knock-out mice showed different extracellular matrix gene expression patterns compared to WT. These findings demonstrate that PLAP-1 enhances adipogenesis and could be a key molecule in understanding the association between periodontal disease and obesity-related metabolic disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipose Tissue / metabolism*
  • Alveolar Bone Loss* / chemically induced
  • Alveolar Bone Loss* / genetics
  • Alveolar Bone Loss* / metabolism
  • Animals
  • Diet, High-Fat / adverse effects*
  • Extracellular Matrix Proteins / deficiency*
  • Extracellular Matrix Proteins / metabolism
  • Metabolic Diseases* / chemically induced
  • Metabolic Diseases* / genetics
  • Metabolic Diseases* / metabolism
  • Mice
  • Mice, Knockout

Substances

  • Aspn protein, mouse
  • Extracellular Matrix Proteins