The effects of radial shock waves on gene transfer in rabbit chondrocytes in vitro

Osteoarthritis and Cartilage

Volumn 15, Issue 11, 2007, Pages 1275-1282

  Murata, R ^a   Nakagawa, K ^a   Ohtori, S ^a   Ochiai, N ^a   Arai, M ^a   Saisu, T ^b   Sasho, T ^a   Takahashi, K ^a   Moriya, H ^a  

^a CHIBA UNIVERSITY   (Japan)

^b CHIBA CHILDREN'S HOSPITAL   (Japan)

Author keywords

Cell viability; Chondrocyte; Gene therapy; Gene transfer; Radial shock waves; Transfection efficiency

Indexed keywords

GREEN FLUORESCENT PROTEIN; LUCIFERASE; PLASMID DNA;

ANIMAL CELL; ARTICLE; CARTILAGE CELL; CELL CULTURE; CELL DISRUPTION; CELL SUSPENSION; CELL VIABILITY; CHONDROPATHY; CONTROLLED STUDY; ENZYME ACTIVITY; FLUORESCENCE ACTIVATED CELL SORTING; GENE EXPRESSION; GENE TRANSFER; GENETIC TRANSFECTION; IN VITRO STUDY; INTERMETHOD COMPARISON; MONOLAYER CULTURE; NONHUMAN; NONVIRAL GENE DELIVERY SYSTEM; NONVIRAL GENE THERAPY; PRIORITY JOURNAL; RABBIT; REPORTER GENE; SHOCK WAVE;

ANIMALS; CARTILAGE, ARTICULAR; CHONDROCYTES; KNEE JOINT; LUCIFERASES; RABBITS; TRANSFECTION; ULTRASONICS;

EID: 35649028894     PISSN: 10634584     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.joca.2007.04.001     Document Type: Article

References (53)

1. Brittberg M., Lindahl A., Nilsson A., Ohlsson C., Isaksson O., and Peterson L. Treatment of deep cartilage defects in the knee with autologous chondrocytes transplantation. N Engl J Med 331 (1994) 889-895
2. Wood J.J., Malek M.A., Frassica F.J., Polder J.A., Mohan A.K., Bloom E.T., et al. Autologous cultured chondrocytes: adverse events reported to the United States Food and Drug Administration. J Bone Joint Surg Am 88 (2006) 503-507
3. Monahan P.E., and Samilski R.J. AAV vectors: is clinical success on the horizon?. Gene Ther 7 (2000) 24-30
4. Tatsis N., and Ertl H.C. Adenoviruses as vaccine vectors. Mol Ther 10 (2004) 616-629
5. Kasper B.K., Roth D.M., Lai N.C., Drumm J.D., Erikson D.A., McKirnan M.D., et al. Myocardial gene transfer and long-term expression following intracoronary delivery of adeno-associated virus. J Gene Med 7 (2005) 316-324
6. Li Y., Tew S.R., Russell A.M., Gonzalez K.R., Hardingham T.E., and Hawkins R.E. Transduction of passaged human articular chondrocytes with adenoviral, retroviral, and lentiviral vectors and the effects of enhanced expression of SOX9. Tissue Eng 10 (2004) 575-584
7. Yokoo N., Saito T., Uesugi M., Kobayashi N., Xin K.Q., Okuda K., et al. Repair of articular cartilage defect by autologous transplantation of basic fibroblast growth factor gene-transduced chondrocytes with adeno-associated virus vector. Arthritis Rheum 52 (2005) 164-170
8. Cucchiarini M., Madry H., Ma C., Thurn T., Zerakowski D., Menger M.D., et al. Improved tissue repair in articular cartilage defects in vivo by rAAV-mediated overexpression of human fibroblast growth factor 2. Mol Ther 12 (2005) 229-238
9. Lu F.Z., Kitazawa Y., Hara Y., Jiang J.Y., and Li X.K. Long-term gene expression using lentiviral vector in rat chondrocytes. Clin Orthop Relat Res 439 (2005) 243-252
10. Navarro J., Oudrhiri N., Fabrega S., and Lehn P. Gene delivery systems: bridging the gap between recombinant viruses and artificial vectors. Adv Drug Deliv Rev 30 (1998) 5-11
11. Yang Y., Nunes F.A., Berencsi K., Furth E.E., Gonczol E., and Wilson J.M. Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc Natl Acad Sci U S A 91 (1994) 4407-4411
12. Yang Y., Jooss K.U., Su Q., Ertl H.C., and Wilson J.M. Immune responses to viral antigens versus transgene product in the elimination of recombinant adenovirus-infected hapatocytes in vivo. Gene Ther 3 (1996) 137-144
13. Ritter T., Lehmann M., and Volk H.D. Improvement in gene therapy: averting the immune response to adenoviral vectors. BioDrugs 16 (2002) 3-10
14. Vile R., and Russell S.J. Gene transfer technologies for the gene therapy of cancer. Gene Ther 1 (1994) 88-98
15. Miller N., and Vile R. Targeted vectors for gene therapy. FASEB J 9 (1995) 190-199
16. Coonrad A., Li F.Q., and Horwitz M. On the mechanism of DNA transfection: efficient gene transfer without viruses. Gene Ther 4 (1997) 1313-1321
17. Fechheimer M., Boylan J.F., Parker S., Sisken J.E., Patel G.L., and Zimmer S.G. Transfection of mammalian cells with plasmid DNA by scrape loading and sonication loading. Proc Natl Acad Sci U S A 84 (1987) 8463-8467
18. Greenleaf W.J., Bolander M.E., Sarker G., Goldring M.B., and Greenleaf J.F. Artificial cavitation nuclei significantly enhance acoustically induced cell transfection. Ultrasound Med Biol 24 (1998) 587-595
19. Danielou G., Comtois A.S., Dudley R.W., Nalbantoglu J., Gilbert R., Karpati G., et al. Ultrasound increases plasmid-mediated gene transfer to dystrophic muscles without collateral damage. Mol Ther 6 (2002) 687-693
20. Gambihler S., Delius M., and Ellwart J.W. Permeabilization of the plasma membrane of L1210 mouse leukemia cells using lithotripter shock waves. J Membr Biol 141 (1994) 267-275
21. Lauer U., Burgelt E., Squire Z., Messmer K., Hofschneider P.H., Gregor M., et al. Shock wave permeabilization as a new gene transfer method. Gene Ther 4 (1997) 710-715
22. Bao S., Thrall B.D., Gies R.A., and Miller D.L. In vivo transfection of melanoma cells by lithotripter shock waves. Cancer Res 58 (1998) 219-221
23. Miller D.L., and Song J. Lithotripter shock waves with cavitation nucleation agents produce tumor growth reduction and gene transfer in vivo. Ultrasound Med Biol 28 (2002) 1343-1348
24. Taniyama Y., Tachibana K., Hiraoka K., Aoki M., Yamamoto S., Matsumoto K., et al. Development of safe and efficient novel nonviral gene transfer using ultrasound: enhancement of transfection efficiency of naked plasmid DNA in skeletal muscle. Gene Ther 9 (2002) 372-380
25. Liang H.D., Lu Q.L., Xue S.A., Halliwell M., Kodama T., Cosgrove D.O., et al. Optimization of ultrasound-mediated gene transfer (sonoporation) in skeletal muscle cells. Ultrasound Med Biol 11 (2004) 1523-1529
26. Lawrie A., Brisken A.F., Francis S.E., Tayler D.I., Chamberlain J., Crossman D.C., et al. Ultrasound enhances reporter gene expression after transfection of vascular cells in vitro. Circulation 99 (1999) 2617-2620
27. Huber P.E., and Pfisterer P. In vitro and in vivo transfection of plasmid DNA in the Dunning prostate tumor R3327-AT1 is enhanced by focused ultrasound. Gene Ther 7 (2000) 1516-1525
28. Guzman H.R., Nguyen D.X., Khan S., and Prausnitz M.R. Ultrasound-mediated disruption of cell membranes. I. Quantification of molecular uptake and cell viability. J Acoust Soc Am 2001 110 (2001) 588-596
29. Huber P.E., Jenne J., Debus J., Wannenmacher M.F., and Pfisterer P. A comparison of shock wave and sinusoidal-focused ultrasound-induced localized transfection of HeLa cells. Ultrasound Med Biol 25 (1999) 1451-1457
30. Da Costa Gomez T.M., Radtke C.L., Kalscheur V.L., Swain C.A., Scolly M.C., Edwards R.B., et al. Effect of focused and radial extracorporeal shock wave therapy on equine bone microdamage. Vet Surg 33 (2004) 49-55
31. Spacca G., Necozione S., and Cacchio A. Radial shock wave therapy for lateral epicondylitis: a prospective randomised controlled single-blind study. Eura Medicophys 41 (2006) 17-25
32. Miller D.L., Bao S., Gies R.A., and Thrall B.D. Ultrasound enhancement of gene transfection in murine melanoma tumors. Ultrasound Med Biol 25 (1999) 1425-1430
33. Schratzberger P., Krainin J.G., Schratzberger G., Silver M., Ma H., Kearney M., et al. Transcutaneous ultrasound augments naked DNA transfection of skeletal muscle. Mol Ther 6 (2002) 576-583
34. Hamm A., Krott N., Breibach I., Blindt R., and Bosserhoff A.K. Efficient transfection method for primary cells. Tissue Eng 8 (2002) 235-245
35. Welter J.F., Solchaga L.A., and Stewart M.C. High-efficiency nonviral transfection of primary chondrocytes. Methods Mol Med 100 (2004) 129-146
36. Apfel R.E. Acoustic cavitation: a possible consequence of bio-medical uses of ultrasound. Br J Cancer Suppl 45 (1982) 140-146
37. Laudone V.P., Morgan T.R., Huryk R.F., Heston W.D., and Fair W.R. Cytotoxicity of high energy shock waves: methodological considerations. J Urol 141 (1989) 965-968
38. Tachibana K., Uchida T., Ogawa K., Yamashita N., and Tamura K. Induction of cell-membrane porosity by ultrasound. Lancet 353 (1999) 1409
39. Huber P., Jochle K., and Debus J. Influence of shock wave pressure amplitude and pulse repetition frequency on the lifespan, size and number of transient cavities in the field of an electromagnetic lithotripter. Phys Med Biol 43 (1998) 3113-3128
40. Yirmaz E., Batislam E., Basar M., Tuglu D., Mert C., and Basar H. Optimal frequency in extracorporeal shock wave lithotripsy: prospective randomized study. Urology 66 (2005) 1160-1164
41. Liu J., Lewis T.N., and Prausnitz M.R. Non-invasive assessment and control of ultrasound-mediated membrane permeabilization. Pharm Res 15 (1998) 918-924
42. Aoyama T., Hosseinkhani H., Yamamoto S., Ogawa O., and Tabata Y. Enhanced expression of plasmid DNA-cationized gelatin complex by ultrasound in murine muscle. J Control Release 80 (2002) 345-356
43. Lu Q.L., Liang H.D., Partridge T., and Blomley M.J. Microbubble ultrasound improves the efficiency of gene transfection in skeletal muscle in vivo with reduced tissue damage. Gene Ther 10 (2003) 396-405
44. 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 towards osteoprogenitors associated with induction of TGF-beta1. J Bone Joint Surg Br 84 (2002) 457-461
45. Takahashi K., Yamazaki M., Saisu T., Nakajima A., Shimizu S., Mitsuhashi S., et al. Gene expression for extracellular matrix proteins in shockwave-induces osteogenesis in rats. Calcif Tissue Int 74 (2004) 187-193
46. Wang C.J., Wang F.S., Yang K.D., Weng L.H., Hsu C.C., Huang C.S., et al. Shock wave therapy induces neovascularization at the tendon-bone junction. A study in rabbits. J Orthop Res 21 (2003) 984-989
47. Wang C.J., Wang F.S., Yang K.D., Weng L.H., Sun Y.C., and Yang Y.J. The effect of shock wave treatment at the tendon-bone interface - an histomorphological and biomechanical study in rabbits. J Orthop Res 23 (2005) 274-280
48. Vaterlein N., Lussenhop S., Hahn M., Delling G., and Meiss A.L. The effect of extracorporeal shock waves on joint cartilage - an in vivo study in rabbits. Arch Orthop Trauma Surg 120 (2000) 403-406
49. Vergunst H., Trepstra O.T., Schroder F.H., and Matura E. In vivo assessment of shock-wave pressure. Implication for biliary lithotripsy. Gastroenterology 99 (1990) 1467-1474
50. Weiss N., Delius M., Gambihler S., Eichholtz-Wirth H., Dirschedl P., and Brendel W. Effect of shock waves and cisplatin on cisplatin-sensitive and -resistant rodent tumors in vitro. Int J Cancer 58 (1994) 693-699
51. Cornel E.B., Smits G.A., Debruyne F.M., Heerschap A., Schalken J.A., and Oosterhof G.O. The effect of successive high-energy shock-wave tumor administration on tumor blood flow. Ultrasound Med Biol 21 (1995) 243-248
52. Gerdesmeyer L., Wagenpfeil S., Haake M., Maier M., Loew M., Wortler K., et al. Extracorporeal shock wave therapy for the treatment of chronic calcifying tendonitis of the rotator cuff: a randomized controlled trial. JAMA 290 (2003) 2573-2580
53. Rompe J.D., Decking J., Schoellner C., and Theis C. Repetitive low-energy shock wave treatment for chronic lateral epicondylitis in tennis players. Am J Sports Med 32 (2004) 734-743