TY - JOUR
T1 - Effect of fluid flow-induced shear stress on the behavior of synovial fibroblasts in a bioinspired synovium-on-chip model
AU - Piluso, Susanna
AU - Li, Yang
AU - Texeira, Liliana Moreira
AU - Padmanaban, Prasanna
AU - Rouwkema, Jeroen
AU - Leijten, Jeroen
AU - van Weeren, René
AU - Karperien, Marcel
AU - Malda, Jos
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/1/9
Y1 - 2025/1/9
N2 - Introduction: Due to the loading of the articular joints and the movement of the joint itself, mechanical stress is constantly exerted on the synovial cavity, which is, in turn, reflected as shear stress toward the surrounding tissues, including the synovium. Although it is known that synovial cells are sensitive to various mechanical cues, deeper understanding on how synovial fibroblasts (SFBs) respond to increased shear stress is required to gain insights on its role in the pathophysiology of osteoarthritis (OA). Objectives: A synovium-on-chip model was developed to evaluate the effect of fluid flow-induced shear stress on fibroblast-like synoviocytes, and to assess the similarities with synovial inflammation during OA. Methods: Patient-derived SFBs were exposed to a shear stress of 3, 8, and 15 dyne/cm2 for up to 72 hours. Production of TNFα, IL-6, MMPs, and lubricin by synovial cells was analyzed. Results: The levels of TNFα, IL-6, and degradative enzymes increased over time when synovial cells were exposed to a shear stress of 8 dyne/cm2. In the first 8 hours, a 5-fold increase in the level of TNFα was observed when the shear stress increased from 3 to 8 dyne/cm2, and a 2-fold increase from shear stress 8 to 15 dyne/cm2. Conclusions: High mechanical stress combined with inflammatory triggers can cause excessive production of cytokines and proteolytic enzymes. Knowledge of how SFBs respond to increasing shear stress contributes to understanding the pathophysiology of OA, in which intra-articular pressure is often elevated, and may contribute to the discovery of potentially effective therapeutic agents.
AB - Introduction: Due to the loading of the articular joints and the movement of the joint itself, mechanical stress is constantly exerted on the synovial cavity, which is, in turn, reflected as shear stress toward the surrounding tissues, including the synovium. Although it is known that synovial cells are sensitive to various mechanical cues, deeper understanding on how synovial fibroblasts (SFBs) respond to increased shear stress is required to gain insights on its role in the pathophysiology of osteoarthritis (OA). Objectives: A synovium-on-chip model was developed to evaluate the effect of fluid flow-induced shear stress on fibroblast-like synoviocytes, and to assess the similarities with synovial inflammation during OA. Methods: Patient-derived SFBs were exposed to a shear stress of 3, 8, and 15 dyne/cm2 for up to 72 hours. Production of TNFα, IL-6, MMPs, and lubricin by synovial cells was analyzed. Results: The levels of TNFα, IL-6, and degradative enzymes increased over time when synovial cells were exposed to a shear stress of 8 dyne/cm2. In the first 8 hours, a 5-fold increase in the level of TNFα was observed when the shear stress increased from 3 to 8 dyne/cm2, and a 2-fold increase from shear stress 8 to 15 dyne/cm2. Conclusions: High mechanical stress combined with inflammatory triggers can cause excessive production of cytokines and proteolytic enzymes. Knowledge of how SFBs respond to increasing shear stress contributes to understanding the pathophysiology of OA, in which intra-articular pressure is often elevated, and may contribute to the discovery of potentially effective therapeutic agents.
KW - Articular joints
KW - In vitro models
KW - Inflammation
KW - Microphysiological systems
KW - Organ-on-chip
KW - Osteoarthritis
UR - http://www.scopus.com/inward/record.url?scp=85215930820&partnerID=8YFLogxK
U2 - 10.1016/j.jcjp.2025.100233
DO - 10.1016/j.jcjp.2025.100233
M3 - Article
AN - SCOPUS:85215930820
SN - 2667-2545
JO - Journal of Cartilage and Joint Preservation
JF - Journal of Cartilage and Joint Preservation
M1 - 100233
ER -