Possible involvement of Opa-interacting protein 5 in adipose proliferation and obesity

PLoS One. 2014 Feb 6;9(2):e87661. doi: 10.1371/journal.pone.0087661. eCollection 2014.

Abstract

Obesity is an epidemic matter increasing risk for cardiovascular diseases and metabolic disorders such as type 2 diabetes. We recently examined the association between visceral fat adiposity and gene expression profile of peripheral blood cells in human subjects. In a series of studies, Opa (Neisseria gonorrhoeae opacity-associated)-interacting protein 5 (OIP5) was nominated as a molecule of unknown function in adipocytes and thus the present study was performed to investigate the role of OIP5 in obesity. Adenovirus overexpressing Oip5 (Ad-Oip5) was generated and infected to 3T3-L1 cells stably expressing Coxsackie-Adenovirus Receptor (CAR-3T3-L1) and to mouse subcutaneous fat. For a knockdown experiment, siRNA against Oip5 (Oip5-siRNA) was introduced into 3T3-L1 cells. Proliferation of adipose cells was measured by BrdU uptake, EdU-staining, and cell count. Significant increase of Oip5 mRNA level was observed in obese white adipose tissues and such increase was detected in both mature adipocytes fraction and stromal vascular cell fraction. Ad-Oip5-infected CAR-3T3-L1 preadipocytes and adipocytes proliferated rapidly, while a significant reduction of proliferation was observed in Oip5-siRNA-introduced 3T3-L1 preadipocytes. Fat weight and number of adipocytes were significantly increased in Ad-Oip5-administered fat tissues. Oip5 promotes proliferation of pre- and mature-adipocytes and contributes adipose hyperplasia. Increase of Oip5 may associate with development of obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adenoviridae / metabolism
  • Adipocytes / metabolism*
  • Adipocytes / pathology
  • Adipose Tissue / metabolism
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Cycle Proteins
  • Cell Proliferation
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosomal Proteins, Non-Histone / metabolism*
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein / metabolism
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / genetics
  • Obesity / pathology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism

Substances

  • Carrier Proteins
  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • Oip5 protein, mouse
  • RNA, Messenger
  • RNA, Small Interfering

Associated data

  • GEO/GSE28038

Grants and funding

This work was supported in part by a Grants-in-Aid for Scientific Research (C) no. 22590979 (to N.M.), a Grants-in-Aid for Scientific Research (B) no. 24390238 (to I.S.), a Grants-in-Aid for Scientific Research on Innovative Areas no. 22126008 (to T.F.), and Takeda Science Foundation (to N.M.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.