Nonpulsed Sinusoidal Electromagnetic Fields as a Noninvasive Strategy in Bone Repair: The Effect on Human Mesenchymal Stem Cell Osteogenic Differentiation

被引:0
作者
Ledda, Mario [1 ]
D'Emilia, Enrico [2 ]
Giuliani, Livio [2 ,3 ]
Marchese, Rodolfo [4 ]
Foletti, Alberto [1 ]
Grimaldi, Settimio [1 ]
Lisi, Antonella [1 ]
机构
[1] CNR, Inst Translat Pharmacol, I-00133 Rome, Italy
[2] Dipartimento Insediamenti Prod & Interaz Con Ambi, Rome, Italy
[3] INAIL Florence, Rome, Italy
[4] FBF S Peter Hosp, Res Ctr, Rome, Italy
关键词
GLUCOCORTICOID-INDUCED OSTEOPOROSIS; MAGNETIC-FIELDS; GENE-EXPRESSION; MOLECULAR-MECHANISMS; OVARIECTOMIZED RATS; RANKL EXPRESSION; STIMULATION; FRACTURES; OSTEOPROTEGERIN; MEDICINE;
D O I
10.1089/ten.tec.2014.0216
中图分类号
Q813 [细胞工程];
学科分类号
摘要
In vivo control of osteoblast differentiation is an important process needed to maintain the continuous supply of mature osteoblast cells for growth, repair, and remodeling of bones. The regulation of this process has also an important and significant impact on the clinical strategies and future applications of cell therapy. In this article, we studied the effect of nonpulsed sinusoidal electromagnetic field radiation tuned at calcium-ion cyclotron frequency of 50 Hz exposure treatment for bone differentiation of human mesenchymal stem cells (hMSCs) alone or in synergy with dexamethasone, their canonical chemical differentiation agent. Five days of continuous exposure to calcium-ion cyclotron resonance affect hMSC proliferation, morphology, and cytoskeletal actin reorganization. By quantitative real-time polymerase chain reaction, we also observed an increase of osteoblast differentiation marker expression such as Runx2, alkaline phosphatase (ALP), osteocalcin (OC), and osteopontin (OPN) together with the osteoprotegerin mRNA modulation. Moreover, in these cells, the increase of the protein expression of OPN and ALP was also demonstrated. These results demonstrate bone commitment of hMSCs through a noninvasive and biocompatible differentiating physical agent treatment and highlight possible applications in new regenerative medicine protocols.
引用
收藏
页码:207 / 217
页数:11
相关论文
共 71 条
[1]   RANKL expression is related to the differentiation state of human osteoblasts [J].
Atkins, GJ ;
Kostakis, P ;
Pan, BQ ;
Farrugia, A ;
Gronthos, S ;
Evdokiou, A ;
Harrison, K ;
Findlay, DM ;
Zannettino, ACW .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (06) :1088-1098
[2]   Clinical significance of different effects of static and pulsed electromagnetic fields on human osteoclast cultures [J].
Barnaba, Simona Angela ;
Ruzzini, Laura ;
Di Martino, Alberto ;
Lanotte, Angela ;
Sgambato, Alessandro ;
Denaro, Vincenzo .
RHEUMATOLOGY INTERNATIONAL, 2012, 32 (04) :1025-1031
[3]   PULSING ELECTROMAGNETIC-FIELD TREATMENT IN UNUNITED FRACTURES AND FAILED ARTHRODESES [J].
BASSETT, CAL ;
MITCHELL, SN ;
GASTON, SR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1982, 247 (05) :623-628
[4]   Phosphate is a specific signal for induction of osteopontin gene expression [J].
Beck, GR ;
Zerler, B ;
Moran, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8352-8357
[5]   CYTOSKELETON AS A TARGET IN MENADIONE-INDUCED OXIDATIVE STRESS IN CULTURED-MAMMALIAN-CELLS .1. BIOCHEMICAL AND IMMUNOCYTOCHEMICAL FEATURES [J].
BELLOMO, G ;
MIRABELLI, F ;
VAIRETTI, M ;
IOSI, F ;
MALORNI, W .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (01) :118-128
[7]   Glucocorticoid-induced osteoporosis: Summary of a workshop [J].
Canalis, E ;
Giustina, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (12) :5681-5685
[8]   Pulsed electromagnetic fields stimulation affects osteoclast formation by modulation of osteoprotegerin, RANK ligand and macrophage colony-stimulating factor [J].
Chang, K ;
Chang, WHS ;
Huang, S ;
Huang, S ;
Shih, C .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2005, 23 (06) :1308-1314
[9]   Effect of pulse-burst electromagnetic field stimulation on osteoblast cell activities [J].
Chang, WHS ;
Chen, LT ;
Sun, JS ;
Lin, FH .
BIOELECTROMAGNETICS, 2004, 25 (06) :457-465
[10]  
Chao Edmund Y S, 2003, Eur Cell Mater, V6, P72