Affiliations 

  • 1 Center for Cellular and Molecular Engineering, Department of Orthopaedic Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15219, USA
  • 2 Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15261, USA
  • 3 Department of Orthopaedic Surgery, Stanford University, Stanford, CA, 94305, USA
  • 4 Institute of Physics, University of Freiburg, Freiburg, 79104, Germany
  • 5 Center for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine, Orleans, LA, 70112, USA
  • 6 Fischell Department of Bioengineering, University of Maryland, College Park, MD, 20742, USA
Adv Sci (Weinh), 2022 Jul;9(21):e2105909.
PMID: 35436042 DOI: 10.1002/advs.202105909

Abstract

Diseases of the knee joint such as osteoarthritis (OA) affect all joint elements. An in vitro human cell-derived microphysiological system capable of simulating intraarticular tissue crosstalk is desirable for studying etiologies/pathogenesis of joint diseases and testing potential therapeutics. Herein, a human mesenchymal stem cell-derived miniature joint system (miniJoint) is generated, in which engineered osteochondral complex, synovial-like fibrous tissue, and adipose tissue are integrated into a microfluidics-enabled bioreactor. This novel design facilitates different tissues communicating while still maintaining their respective phenotypes. The miniJoint exhibits physiologically relevant changes when exposed to interleukin-1β mediated inflammation, which are similar to observations in joint diseases in humans. The potential of the miniJoint in predicting in vivo efficacy of drug treatment is confirmed by testing the "therapeutic effect" of the nonsteroidal anti-inflammatory drug, naproxen, as well as four other potential disease-modifying OA drugs. The data demonstrate that the miniJoint recapitulates complex tissue interactions, thus providing a robust organ chip model for the study of joint pathology and the development of novel therapeutic interventions.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.