Aging along with inflammation, infection, and trauma can all cause damage to joint tissue resulting in arthritic disorders. These disorders can be debilitating, significantly impacting on quality of life.
A team of University of Pittsburgh researchers have developed a 3D human micro-joint chip (mJoint) physiologically analogous to joints and capable of modelling pathogenesis of joint disease to allow for the development of disease-modifying medications (DMMs) for arthritic disorders.
A personalizable 3D mJoint containing all components of a human joint including cartilage, bone, synovium, and infrapatellar fat pad (IPFP).
Previous research into DMMs for OA and other arthritic joint conditions has focused on specific tissue components of the joint. However, OA is now understood to be an organ disease affecting multiple tissues and systemic influences.
Other research has used young animal models, the results of which are not directly translatable to clinical trials on age- or obesity-associated OA.
This new preclinical model will overcome the existing challenges in current models using a personalizable 3D mJoint containing all components of a human joint including cartilage, bone, synovium, and infrapatellar fat pad (IPFP). The mJoint aims to replicate the in vivo conditions in human OA and other arthritic conditions, meaning experimental results will be more clinically relevant.
Hang Lin, PhD | Department of Orthopaedic Surgery | University of Pittsburgh
Peter Alexander, PhD | Department of Orthopaedic Surgery | University of Pittsburgh
Riccardo Luca Gottardi, PhD
Rocky Sung Chi Tuan, PhD