@article {20428, title = {Magnetic responsive materials modulate the inflammatory profile of IL-1β conditioned tendon cells}, journal = {Acta Biomaterialia}, volume = {117}, year = {2020}, month = {2020-09-15 00:00:00}, pages = {235-245}, abstract = {

Tendinopathies represent half of all musculoskeletal injuries worldwide. Inflammatory events contribute to both tendon healing and to tendinopathy conditions but the cellular triggers leading to one or the other are unknown. In previous studies, we showed that magnetic field actuation modulates human tendon cells (hTDCs) behavior in pro-inflammatory environments, and that magnetic responsive membranes could positively influence inflammation responses in a rat ectopic model.

Herein, we propose to investigate the potential synergistic action of the magnetic responsive membranes, made of a polymer blend of starch with polycaprolactone incorporating magnetic nanoparticles (magSPCL), and the actuation of pulsed electromagnetic field (PEMF): 5\ Hz, 4mT of intensity and 50\% of duty cycle, in IL-1β-treated-hTDCs, and in the immunomodulatory response of macrophages.

It was found that the expression of pro-inflammatory (TNFα, IL-6, IL-8, COX-2) and ECM remodeling (MMP-1,-2,-3) markers tend to decrease in cells cultured onto magSPCL membranes under PEMF, while the expression of TIMP-1 and anti-inflammatory genes (IL-4, IL-10) increases. Also, CD16++\ and CD206+\ macrophages were only found on magSPCL membranes with PEMF application.

Magnetic responsive membranes show a modulatory effect on the inflammatory profile of hTDCs favoring anti-inflammatory cues which is also supported by the anti-inflammatory/repair markers expressed in macrophages. These results suggest that magnetic responsive magSPCL membranes can contribute for inflammation resolution acting on both resident cell populations and inflammatory cells, and thus significantly contribute to tendon regenerative strategies.

}, keywords = {Inflammatory environmental cues, Magnetic platforms, Magnetic responsive membranes, Nanoparticles, tendon cells}, issn = {1742-7061}, doi = {10.1016/j.actbio.2020.09.028}, url = {https://doi.org/10.1016/j.actbio.2020.09.028}, author = {Vinhas, A. and Rodrigues, M. T. and Gon{\c c}alves, A. I. and Reis, R. L. and Gomes, M. E.} }