Pulsed Electromagnetic Field Stimulation in Osteogenesis and Chondrogenesis: Signaling Pathways and Therapeutic Implications

被引:64
作者
Varani, Katia [1 ]
Vincenzi, Fabrizio [1 ]
Pasquini, Silvia [1 ]
Blo, Irene [2 ]
Salati, Simona [3 ]
Cadossi, Matteo [3 ]
De Mattei, Monica [2 ]
机构
[1] Univ Ferrara, Dept Translat Med & Romagna, I-44121 Ferrara, Italy
[2] Univ Ferrara, Dept Med Sci, I-44121 Ferrara, Italy
[3] IGEA SpA, Clin Biophys, I-41012 Carpi, Italy
关键词
mesenchymal stem cells; pulsed electromagnetic fields; osteogenic differentiation; chondrogenic differentiation; tissue engineering; adenosine receptors; MESENCHYMAL STEM-CELLS; HUMAN BONE-MARROW; ADENOSINE RECEPTORS; STROMAL CELLS; ION CHANNELS; DIFFERENTIATION; REPAIR; OSTEOARTHRITIS; PROLIFERATION; CHONDROCYTES;
D O I
10.3390/ijms22020809
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem cells (MSCs) are the main cell players in tissue repair and thanks to their self-renewal and multi-lineage differentiation capabilities, they gained significant attention as cell source for tissue engineering (TE) approaches aimed at restoring bone and cartilage defects. Despite significant progress, their therapeutic application remains debated: the TE construct often fails to completely restore the biomechanical properties of the native tissue, leading to poor clinical outcomes in the long term. Pulsed electromagnetic fields (PEMFs) are currently used as a safe and non-invasive treatment to enhance bone healing and to provide joint protection. PEMFs enhance both osteogenic and chondrogenic differentiation of MSCs. Here, we provide extensive review of the signaling pathways modulated by PEMFs during MSCs osteogenic and chondrogenic differentiation. Particular attention has been given to the PEMF-mediated activation of the adenosine signaling and their regulation of the inflammatory response as key player in TE approaches. Overall, the application of PEMFs in tissue repair is foreseen: (1) in vitro: to improve the functional and mechanical properties of the engineered construct; (2) in vivo: (i) to favor graft integration, (ii) to control the local inflammatory response, and (iii) to foster tissue repair from both implanted and resident MSCs cells.
引用
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页码:1 / 17
页数:17
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