Extracorporeal Shock Waves Stimulate Osteoblast Activities

Ultrasound in Medicine and Biology

Volumn 35, Issue 12, 2009, Pages 2093-2100

  Tamma, Roberto ^a   dell'Endice, Stefania ^a   Notarnicola, Angela ^a   Moretti, Lorenzo ^a   Patella, Silvio ^a   Patella, Vittorio ^a   Zallone, Alberta ^a   Moretti, Biagio ^a,b  

^a UNIVERSITY OF BARI   (Italy)

^b SITOD   (Italy)

Author keywords

Osteoblasts; Osteogenesis; Shockwaves

Indexed keywords

AFTER-TREATMENT; BONE REPAIR; CELLULAR MECHANISMS; ELECTROMAGNETIC DEVICES; EXTRACORPOREAL SHOCKWAVE THERAPY; MURINE OSTEOBLASTS; MUSCULOSKELETAL DISORDERS; OSTEOCLASTOGENESIS; OSTEOGENESIS; OSTEOPROTEGERIN; PRO-APOPTOTIC EFFECTS; REAL-TIME POLYMERASE CHAIN REACTION; RECEPTOR ACTIVATOR; WESTERN-BLOT ANALYSIS;

BONE; BOTTLES; CELL CULTURE; CELL PROLIFERATION; CHEMICAL ACTIVATION; ELECTROMAGNETS; SHOCK WAVES;

OSTEOBLASTS;

CYCLIN DEPENDENT KINASE 2; CYCLINE; OSTEOCLAST DIFFERENTIATION FACTOR; OSTEOPROTEGERIN; PROTEIN BAX;

ANIMAL CELL; ANIMAL CELL CULTURE; ARTICLE; BONE DEVELOPMENT; CELL ACTIVITY; CELL CYCLE G1 PHASE; CELL CYCLE REGULATION; CELL CYCLE S PHASE; CELL PROLIFERATION; CELL STIMULATION; CONTROLLED STUDY; ENZYME ACTIVATION; EXTRACORPOREAL LITHOTRIPSY; MAGNETIC AND ELECTROMAGNETIC EQUIPMENT; MOUSE; NONHUMAN; OSTEOBLAST; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN SECRETION; REAL TIME POLYMERASE CHAIN REACTION; WESTERN BLOTTING;

ANIMALS; CELL PROLIFERATION; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, RADIATION; MICE; MICE, INBRED C57BL; OSTEOBLASTS; OSTEOGENESIS; RADIATION DOSAGE; SONICATION;

EID: 71749121778     PISSN: 03015629     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ultrasmedbio.2009.05.022     Document Type: Article

References (32)

1. Gebken J., Luders B., Notbohm H., Klein H.H., Brinckmann J., Müller P.K., and Bätge B. Hypergravity stimulates collagen synthesis in human osteoblast-like cells: Evidence for the involvement of p44/42 MAP-kinases (ERK 1/2). J Biochem 126 (1999) 676-678
2. Graff J., Pastor J., Funke P.J., Mach P., and Senge T. Extracorporeal shock wave lithotripsy for ureteral stones: A retrospective analysis of 417 cases. J Urol 139 (1988) 513-516
3. Haupt G., and Chvapil M. Effect of shock waves on the healing of partial-thickness wounds in piglets. J Surg Res 49 (1990) 45-48
4. Hofmann A., Ritz U., Hessmann M.H., Alini M., Rommens P.M., and Rompe J. Extracorporeal shock wave-mediated changes in proliferation, differentiation, and gene expression of human osteoblasts. J Trauma Inj Infect Crit Care 65 (2008) 1402-1410
5. Ikeda K., Tomita K., and Takayama K. Application of extracorporeal shock wave on bone: preliminary report. J Trauma 47 (1999) 946-950
6. Jessop H.L., Rawlinson S.C., Pitsillides A.A., and Lanyon L.E. Mechanical strain and fluid movement both activate extracellular regulated kinase (ERK) in osteoblast-like cells but via different signaling pathways. Bone 31 (2002) 186-194
7. Karsenty G. Minireview: Transcriptional control of osteoblast differentiation. Endocrinology 142 (2001) 2731-2733
8. Kaulesar Johannes E.J., Sukul D.M., Bijma A.M., and Mulder P.G. Effects of high-energy shockwaves on normal human fibroblasts in suspension. J Surg Res 57 (1994) 677-681
9. Kern B., Shen J., Starbuck M., and Karsenty G. Cbfa1 contributes to the osteoblast-specific expression of type I collagen genes. J Biol Chem 276 (2001) 7101-7107
10. Lai C.F., Chaudhar L.Y., Fausto A., Halstead L.R., Ory D.S., Avioli L.V., and Cheng S.L. Erk is essential for growth, differentiation, integrin expression, and cell function in human osteoblastic cells. J Biol Chem 276 (2001) 14443-14450
11. Lou J., Tu Y., and Manske P.R. Involvement of ERK in BMP-2 induced osteoblastic differentiation of mesenchymal progenitor cell line C3H10T1/2. Biochem Biophys Res Commun 268 (2000) 757-762
12. Maier M., Milz S., Tischer T., Münzing W., Manthey N., Stäbler A., Holzknecht N., Weiler C., Nerlich A., Refior H.J., and Schmitz C. Influence of extracorporeal shock-wave application on normal bone in an animal model in vivo. Scintigraphy, MRI and histopathology. J Bone Joint Surg Br 84 (2002) 592-599
13. Martini L., Fini M., Giavaresi G., Torricelli P., de Pretto M., Rimondini L., and Giardino R. Primary osteoblasts response to shock wave therapy using different parameters. Artif Cells Blood Substit Immobil Biotechnol 31 (2003) 449-466
14. Martini L., Giavaresi G., Fini M., Torricelli P., De Pretto M., Schaden W., and Giardino R. Effect of extracorporeal shock wave therapy on osteoblastlike cells. Clin Orthop Relat Res 413 (2003) 269-280
15. Martini L., Giavaresi G., Fini M., Borsari V., Torricelli P., and Giardino R. Early effects of extracorporeal shock wave treatment on osteoblast-like cells: A comparative study between electromagnetic and electrohydraulic devices. J Trauma 61 (2006) 1198-1206
16. Marzo I., Brenner C., Zamzami N., Jürgensmeier J.M., Susin S.A., Vieira H.L., Prévost M.C., Xie Z., Matsuyama S., Reed J.C., and Kroemer G. Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis. Science 281 (1998) 2027-2031
17. Meloche S., and Pouyssegur J. The ERK1/2 mitogen-activated protein kinase pathway as a master regulator of the G1- to S-phase transition. Oncogene 26 (2007) 3227-3239
18. Meirer R., Brunner A., Deibl M., Oehlbauer M., Piza-Katzer H., and Kamelger F.S. Shock wave therapy reduces necrotic flap zones and induces VEGF expression in animal epigastric skin flap model. J Reconstr Microsurg 23 (2007) 231-236
19. Narita M., Shimizu S., Ito T., Chittenden T., Lutz R.J., Matsuda H., and Tsujimoto Y. Bax interacts with the permeability transition pore to induce permeability transition and cytochrome c release in isolated mitochondria. Proc Natl Acad Sci USA 95 (1998) 14681-14686
20. Nishida T., Shimokawa H., Oi K., Tatewaki H., Uwatoku T., Abe K., Matsumoto Y., Kajihara N., Eto M., Matsuda T., Yasui H., Takeshita A., and Sunagawa K. Extracorporeal cardiac shock wave therapy markedly ameliorates ischemia-induced myocardial dysfunction in pigs in vivo. Circulation 110 (2004) 3055-3061
21. Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29 (2001) e45
22. Roberts P.J., and Der C.J. Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer. Oncogene 26 (2007) 3291-3310
23. Rogers A., and Eastell R. Circulating osteoprotegerin and receptor activator for nuclear factor κB ligand: Clinical utility in metabolic bone disease assessment. J Clin Endocrinol Metab 90 (2005) 6323-6331
24. Rompe J.D., Zoellner J., and Nafe B. Shock wave therapy versus conventional surgery in the treatment of calcifying tendinitis of the shoulder. Clin Orthop Relat Res 387 (2001) 72-82
25. Tischer T., Milz S., Weiler C., Pautke C., Hausdorf J., Schmitz C., and Maier M. Dose-dependent new bone formation by extracorporeal shock wave application on the intact femur of rabbits. Eur Surg Res 41 (2008) 44-53
26. Wada T., Nakashima T., Hiroshi N., and Penninger J.M. RANKL-RANK signaling in osteoclastogenesis and bone disease. Trends Mol Med 12 (2006) 17-25
27. Wang C.J. An overview of shock wave therapy in musculoskeletal disorders. Chang Gung Med J 26 (2003) 220-232
28. Wang F.S., Wang C.J., Huang H.J., Chung H., Chen R.F., and Yang K.D. Physical shock wave mediates membrane hyperpolarization and Ras activation for osteogenesis in human bone marrow stromal cells. Biochem Biophys Res Commun 287 (2001) 648-655
29. Wang F.S., Yang K.D., Chen R.F., Wang C.J., and Sheen-Chen S.M. Extracorporeal shock wave promotes growth and differentiation of bone-marrow stromal cells toward osteoprogenitors associated with induction of TGF-beta1. J Bone Joint Surg Br 84 (2002) 457-461
30. Wei M.C., Zong W.X., Cheng E.H., Lindsten T., Panoutsakopoulou V., Ross A.J., Roth K.A., Macgregor G.R., Thompson C.B., and Korsmeyer S.J. Proapoptotic Bax And Bak: A requisite gateway to mitochondrial dysfunction and death. Science 292 (2001) 727-730
31. Xiao G., Jiang D., Thomas P., Benson M.D., Guan K., Karsenty G., and Franceschi R.T. mMAPK pathways activate and phosphorylate the osteoblast-specific transcription factor, Cbfa1. J Biol Chem 275 (2000) 4453-4459
32. Yao C.Z., Ishizuka J., Bold R.J., Townsend C.M., and Thompson J.C. Cytocidal effect of high energy shock wave on tumour cells enhanced with larger dose and multiple exposures. Surg Oncol 3 (1994) 229-235