A Tympanic Piezo‐Bioreactor Modulates Ion Channel‐Associated Mechanosignaling to Stabilize Phenotype and Promote Tenogenesis in Human Tendon‐Derived Cells

• Published in: Advanced science 2024-12, Vol.11 (45), p.e2405711-n/a
• Main Authors: Fernandez‐Yague, Marc A., Palma, Matteo, Tofail, Syed A. M., Duffy, Maeve, Quinlan, Leo R., Dalby, Mathew J., Pandit, Abhay, Biggs, Manus J.
• Format: Article
• Language: English
• Subjects: Annealing; Bioreactors; BNNT; Boron; Cell Differentiation - physiology; Cells, Cultured; Crystals; Electric fields; electromechanical; FAK; Fluorides; focal adhesions; Fourier transforms; Genetic engineering; Humans; Ion Channels - genetics; Ion Channels - metabolism; mechanotransduction; Mechanotransduction, Cellular - physiology; Phenotype; piezoelectricity; PVDF‐TrFE; tendon; Tendons - cytology; Tendons - metabolism; Tympanic Membrane - metabolism
• ISSN: 2198-3844; 2198-3844
• DOI: 10.1002/advs.202405711

Preserving the function of human tendon‐derived cells (hTDCs) during cell expansion is a significant challenge in regenerative medicine. In this study, a non‐genetic approach is introduced to control the differentiation of hTDCs using a newly developed tympanic bioreactor. The system mimics the functionality of the human tympanic membrane, employing a piezoelectrically tuned acoustic diaphragm made of polyvinylidene fluoride‐co‐trifluoroethylene and boron nitride nanotubes. The diaphragm is vibrationally actuated to deliver targeted electromechanical stimulation to hTDCs. The results demonstrate that the system effectively maintains the tendon‐specific phenotype of hTDCs, even under conditions that typically induce nonspecific differentiation, such as osteogenesis. This stabilization is achieved by modulating integrin‐mediated mechanosignaling via ion channel‐regulated calcium activity, potentially by TREK‐1 and PIEZO1, yet targeted studies are required for confirmation. Finally, the system sustains the activation of key differentiation pathways (bone morphogenetic protein, BMP) while downregulating osteogenesis‐associated (mitogen‐ctivated protein kinase, MAPK and wingless integrated, WNT) pathways and upregulating Focal Adhesion Kinase (FAK) signaling. This approach offers a finely tunable, dose‐dependent control over hTDC differentiation, presenting significant potential for non‐genetic approaches in cell therapy, tendon tissue engineering, and the regeneration of other mechanosensitive tissues. Membrane receptors such as the ion channels PIEZO1 or TREK‐1 influence transcriptional activity. Under normal physiological “electro‐mechanical” conditions, ion channel activity is regulated, limiting calcium influx and mantaining membrane potential. However, in response to injury or excesive mechanical forces, calcium activity increases byunregulated ion channel activitydeactivating tendon‐specific transcriptional activity.