Identification of novel adipokines in the joint. Differential expression in healthy and osteoarthritis tissues

PLoS One. 2015 Apr 8;10(4):e0123601. doi: 10.1371/journal.pone.0123601. eCollection 2015.

Abstract

Objectives: Emerging data suggest that several metabolic factors, released mainly by white adipose tissue (WAT) and joint tissues, and collectively named adipokines, might have a role in the pathophysiology of OA. Recently, novel adipokines such as SERPINE2, WISP2, GPNMB and ITIH5 have been identified in WAT. The main goal of this study was to analyse the expression of these novel adipokines in synovium, infrapatellar fat pad and chondrocytes and to compare the expression of these molecules in healthy and OA tissues.

Methods: Synovial tissues, infrapatellar fat pad and chondrocytes were obtained from 36 OA patients (age 52-85; mean BMI 28.9) who underwent total knee replacement surgery. Healthy synovial tissues and infrapatellar fat pad were obtained from 15 traumatic knee patients (age 23-53; mean BMI 23.5). mRNA and protein expression were determined by qRT-PCR and western blot analysis respectively.

Results: All the novel adipokines, matter of our study, are expressed in OA synovium, infrapatellar fat pad and chondrocytes. Moreover, we detected a differential expression of SERPINE2 and ITIH5 in OA synovial tissues as compared to healthy samples. Finally, we also observed an increased expression of WISP2 in OA infrapatellar fat pad in comparison to healthy controls.

Conclusions: In this study we demonstrated for the first time the expression of four novel adipokines in different joint tissues and how these molecules are differentially expressed in healthy and OA joint tissues.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipokines / genetics
  • Adipokines / metabolism*
  • Adipose Tissue / metabolism
  • Adult
  • Aged
  • Aged, 80 and over
  • Arthroplasty, Replacement, Knee
  • CCN Intercellular Signaling Proteins / genetics
  • CCN Intercellular Signaling Proteins / metabolism
  • Gene Expression
  • Humans
  • Knee Joint / metabolism*
  • Knee Joint / pathology
  • Knee Joint / surgery
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Middle Aged
  • Osteoarthritis, Knee / metabolism*
  • Osteoarthritis, Knee / surgery
  • Proteinase Inhibitory Proteins, Secretory / genetics
  • Proteinase Inhibitory Proteins, Secretory / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Serpin E2 / genetics
  • Serpin E2 / metabolism
  • Young Adult

Substances

  • Adipokines
  • CCN Intercellular Signaling Proteins
  • CCN5 protein, human
  • GPNMB protein, human
  • ITIH5 protein, human
  • Membrane Glycoproteins
  • Proteinase Inhibitory Proteins, Secretory
  • Repressor Proteins
  • SERPINE2 protein, human
  • Serpin E2

Grants and funding

OG is Staff Personnel of Xunta de Galicia (SERGAS) through a research-staff stabilization contract (ISCIII/SERGAS). OG is supported by Instituto de Salud Carlos III (PI11/01073) Oreste Gualillo is a member of RETICS Programme, RD12/0009/0008 (RIER:Red de Investigación en Inflamación y Enfermedades Reumáticas) via Instituto de Salud Carlos III (ISCIII). Morena Scotece is a recipient of the “FPU” programme of the Spanish Ministry of Education. Javier Conde is a recipìent of a predoctoral program of Fundación Ramón Domínguez. Vanessa Abella is a predoctoral recipient of Xunta de Galicia. Veronica Lopez is a recipient of a grant from ISCIII. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.