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A Combinational Therapy of Articular Cartilage Defects: Rapid and Effective Regeneration by Using Low-Intensity Focused Ultrasound After Adipose Tissue-Derived Stem Cell Transplantation

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Tissue Engineering and Regenerative Medicine Aims and scope

Abstract

Background:

Although low-intensity pulsed ultrasound has been reported to be potential cartilage regeneration, there still unresolved treatment due to cartilage fibrosis and degeneration by a lack of rapid and high-efficiency treatment. The purpose of this study was to investigate the effect of a combination therapy of focused acoustic force and stem cells at site for fast and efficient healing on cartilage regeneration.

Methods:

Using a rat articular cartilage defects model, one million adipose tissue-derived stem cells (ASCs) were injected into the defect site, and low-intensity focused ultrasound (LOFUS) in the range of 100–600 mV was used for 20 min/day for 2 weeks. All experimental groups were sacrificed after 4 weeks in total. The gross appearance score and hematoxylin and eosin (H&E), Alcian blue, and Safranin O staining were used for measuring the chondrogenic potential. The cartilage characteristics were observed, and type II collagen, Sox 9, aggrecan, and type X collagen were stained with immunofluorescence. The results of the comprehensive analysis were calculated using the Mankin scoring method.

Results:

The gross appearance scores of regenerated cartilage and chondrocyte-like cells in H&E images were higher in LOFUS-treated groups compared to those in negative control or ASC-treated groups. Safranin O and Alcian blue staining demonstrated that the 100 and 300 mV LOFUS groups showed greater synthesis of glycosaminoglycan and proteoglycan. The ASC + LOFUS 300 mV group showed positive regulation of type II collagen, Sox 9 and aggrecan and negative regulation of type X collagen, which indicated the occurrence of cartilage regeneration based on the Mankin score result.

Conclusion:

The combination therapy, which involved treatment with ASC and 300 mV LOFUS, quickly and effectively reduced articular cartilage defects.

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References

  1. Goldring MB, Goldring SR. Articular cartilage and subchondral bone in the pathogenesis of osteoarthritis. Ann N Y Acad Sci. 2010;1192:230–7.

    Article  CAS  PubMed  Google Scholar 

  2. Wang M, Yuan Z, Ma N, Hao C, Guo W, Zou G, et al. Advances and prospects in stem cells for cartilage regeneration. Stem Cells Int. 2017;2017:4130607.

    PubMed  PubMed Central  Google Scholar 

  3. Yelin E. Cost of musculoskeletal diseases: impact of work disability and functional decline. J Rheumatol Suppl. 2003;68:8–11.

    PubMed  Google Scholar 

  4. Song H, Song BW, Cha MJ, Choi IG, Hwang KC. Modification of mesenchymal stem cells for cardiac regeneration. Expert Opin Biol Ther. 2010;10:309–19.

    Article  PubMed  Google Scholar 

  5. Dulak J, Szade K, Szade A, Nowak W, Józkowicz A. Adult stem cells: hopes and hypes of regenerative medicine. Acta Biochim Pol. 2015;62:329–37.

    Article  CAS  PubMed  Google Scholar 

  6. Chu DT, Nguyen Thi Phuong T, Tien NLB, Tran DK, Minh LB, Thanh VV, et al. Adipose tissue stem cells for therapy: an update on the progress of isolation, culture, storage, and clinical application. J Clin Med. 2019;8:917.

    Article  CAS  PubMed Central  Google Scholar 

  7. Han S, Sun HM, Hwang KC, Kim SW. Adipose-derived stromal vascular fraction cells: update on clinical utility and efficacy. Crit Rev Eukaryot Gene Expr. 2015;25:145–52.

    Article  PubMed  Google Scholar 

  8. Osinga R, Di Maggio N, Todorov A, Allafi N, Barbero A, Laurent F, et al. Generation of a bone organ by human adipose-derived stromal cells through endochondral ossification. Stem Cells Transl Med. 2016;5:1090–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Stromps JP, Paul NE, Rath B, Nourbakhsh M, Bernhagen J, Pallua N. Chondrogenic differentiation of human adipose-derived stem cells: a new path in articular cartilage defect management? Biomed Res Int. 2014;2014:740926.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Shafaei H, Esfandiari E, Esmaeili A, Razavi S, Hashemibeni B, Nasr Esfahani MH, et al. Optimizing a novel method for low intensity ultrasound in chondrogenesis induction. Adv Biomed Res. 2013;2:79.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Angele P, Schumann D, Angele M, Kinner B, Englert C, Hente R, et al. Cyclic, mechanical compression enhances chondrogenesis of mesenchymal progenitor cells in tissue engineering scaffolds. Biorheology. 2004;41:335–46.

    CAS  PubMed  Google Scholar 

  12. Huang CY, Reuben PM, Cheung HS. Temporal expression patterns and corresponding protein inductions of early responsive genes in rabbit bone marrow-derived mesenchymal stem cells under cyclic compressive loading. Stem Cells. 2005;23:1113–21.

    Article  CAS  PubMed  Google Scholar 

  13. Korstjens CM, van der Rijt RH, Albers GH, Semeins CM, Klein-Nulend J. Low-intensity pulsed ultrasound affects human articular chondrocytes in vitro. Med Biol Eng Comput. 2008;46:1263–70.

    Article  CAS  PubMed  Google Scholar 

  14. Padilla F, Puts R, Vico L, Guignandon A, Raum K. Stimulation of bone repair with ultrasound. Adv Exp Med Biol. 2016;880:385–427.

    Article  CAS  PubMed  Google Scholar 

  15. Wang X, Lin Q, Zhang T, Wang X, Cheng K, Gao M, et al. Low-intensity pulsed ultrasound promotes chondrogenesis of mesenchymal stem cells via regulation of autophagy. Stem Cell Res Ther. 2019;10:41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Xia P, Wang X, Qu Y, Lin Q, Cheng K, Gao M, et al. TGF-β1-induced chondrogenesis of bone marrow mesenchymal stem cells is promoted by low-intensity pulsed ultrasound through the integrin-mTOR signaling pathway. Stem Cell Res Ther. 2017;8:281.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  17. Li X, Li J, Cheng K, Lin Q, Wang D, Zhang H, et al. Effect of low-intensity pulsed ultrasound on MMP-13 and MAPKs signaling pathway in rabbit knee osteoarthritis. Cell Biochem Biophys. 2011;61:427–34.

    Article  CAS  PubMed  Google Scholar 

  18. Vaughan NM, Grainger J, Bader DL, Knight MM. The potential of pulsed low intensity ultrasound to stimulate chondrocytes matrix synthesis in agarose and monolayer cultures. Med Biol Eng Comput. 2010;48:1215–22.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Kusuyama J, Bandow K, Shamoto M, Kakimoto K, Ohnishi T, Matsuguchi T. Low intensity pulsed ultrasound (LIPUS) influences the multilineage differentiation of mesenchymal stem and progenitor cell lines through ROCK-Cot/Tpl2-MEK-ERK signaling pathway. J Biol Chem. 2014;289:10330–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Ebisawa K, Hata K, Okada K, Kimata K, Ueda M, Torii S, et al. Ultrasound enhances transforming growth factor beta-mediated chondrocyte differentiation of human mesenchymal stem cells. Tissue Eng. 2004;10:921–9.

    Article  CAS  PubMed  Google Scholar 

  21. Lynn JG, Zwemer RL, Chick AJ, Miller AE. A new method for the generation and use of focused ultrasound in experimental biology. J Gen Physiol. 1942;26:179–93.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Lee J, Lee S, Lee CY, Seo HH, Shin S, Choi JW, et al. Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death. Stem Cell Res Ther. 2017;8:195.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Choi E, Lee J, Lee S, Song BW, Seo HH, Cha MJ, et al. Potential therapeutic application of small molecule with sulfonamide for chondrogenic differentiation and articular cartilage repair. Bioorg Med Chem Lett. 2016;26:5098–102.

    Article  CAS  PubMed  Google Scholar 

  24. Lee JH, Hong HK, Song BW, Jung YJ, Na YC, Kim NH, et al. Preliminary study on low intensity focused ultrasound system for neuromodulation. Conf Proc IEEE Eng Med Biol Soc. 2017;2017:4545–8.

    Google Scholar 

  25. Carranza-Bencano A, García-Paino L, Armas Padrón JR, Cayuela Dominguez A. Neochondrogenesis in repair of full-thickness articular cartilage defects using free autogenous periosteal grafts in the rabbit. A follow-up in six months. Osteoarthritis Cartilage. 2000;8:351–8.

    Article  CAS  PubMed  Google Scholar 

  26. Moussavi-Harami SF, Pedersen DR, Martin JA, Hillis SL, Brown TD. Automated objective scoring of histologically apparent cartilage degeneration using a custom image analysis program. J Orthop Res. 2009;27:522–8.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Zheng L, Pi C, Zhang J, Fan Y, Cui C, Zhou Y, et al. Aberrant activation of latent transforming growth factor-β initiates the onset of temporomandibular joint osteoarthritis. Bone Res. 2018;6:26.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  28. Grande DA, Southerland SS, Manji R, Pate DW, Schwartz RE, Lucas PA. Repair of articular cartilage defects using mesenchymal stem cells. Tissue Eng. 1995;1:345–53.

    Article  CAS  PubMed  Google Scholar 

  29. Im GI, Kim DY, Shin JH, Hyun CW, Cho WH. Repair of cartilage defect in the rabbit with cultured mesenchymal stem cells from bone marrow. J Bone Joint Surg Br. 2001;83:289–94.

    Article  CAS  PubMed  Google Scholar 

  30. Lee KB, Hui JH, Song IC, Ardany L, Lee EH. Injectable mesenchymal stem cell therapy for large cartilage defects–a porcine model. Stem Cells. 2007;25:2964–71.

    Article  PubMed  Google Scholar 

  31. Khanmohammadi M, Golshahi H, Saffarian Z, Montazeri S, Khorasani S, Kazemnejad S. Repair of osteochondral defects in rabbit knee using menstrual blood stem cells encapsulated in fibrin glue: a good stem cell candidate for the treatment of osteochondral defects. Tissue Eng Regen Med. 2019;16:311–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. de Windt TS, Vonk LA, Slaper-Cortenbach IC, van den Broek MP, Nizak R, van Rijen MH, et al. Allogeneic mesenchymal stem cells stimulate cartilage regeneration and are safe for single-stage cartilage repair in humans upon mixture with recycled autologous chondrons. Stem Cells. 2017;35:256–64.

    Article  PubMed  CAS  Google Scholar 

  33. Awad ME, Hussein KA, Helwa I, Abdelsamid MF, Aguilar-Perez A, Mohsen I, et al. Meta-analysis and evidence base for the efficacy of autologous bone marrow mesenchymal stem cells in knee cartilage repair: methodological guidelines and quality assessment. Stem Cells Int. 2019;2019:3826054.

    Article  PubMed  PubMed Central  Google Scholar 

  34. O'Brien WD Jr. Ultrasound-biophysics mechanisms. Prog Biophys Mol Biol. 2007;93:212–55.

    Article  PubMed  Google Scholar 

  35. Jingushi S, Mizuno K, Matsushita T, Itoman M. Low-intensity pulsed ultrasound treatment for postoperative delayed union or nonunion of long bone fractures. J Orthop Sci. 2007;12:35–41.

    Article  PubMed  Google Scholar 

  36. Harrison A, Lin S, Pounder N, Mikuni-Takagaki Y. Mode & mechanism of low intensity pulsed ultrasound (LIPUS) in fracture repair. Ultrasonics. 2016;70:45–52.

    Article  CAS  PubMed  Google Scholar 

  37. Xiao W, Xu Q, Zhu Z, Li L, Chen W. Different performances of CXCR4, integrin-1β and CCR-2 in bone marrow stromal cells (BMSCs) migration by low-intensity pulsed ultrasound stimulation. Biomed Tech (Berl). 2017;62:89–95.

    Article  CAS  Google Scholar 

  38. Xia P, Shen S, Lin Q, Cheng K, Ren S, Gao M, et al. Low-intensity pulsed ultrasound treatment at an early osteoarthritis stage protects rabbit cartilage from damage via the integrin/focal adhesion kinase/mitogen-activated protein kinase signaling pathway. J Ultrasound Med. 2015;34:1991–9.

    Article  PubMed  Google Scholar 

  39. Muttigi MS, Kim BJ, Choi B, Yoshie A, Kumar H, Han I, et al. Matrilin-3 codelivery with adipose-derived mesenchymal stem cells promotes articular cartilage regeneration in a rat osteochondral defect model. J Tissue Eng Regen Med. 2018;12:667–75.

    Article  CAS  PubMed  Google Scholar 

  40. Tyler WJ, Tufail Y, Finsterwald M, Tauchmann ML, Olson EJ, Majestic C. Remote excitation of neuronal circuits using low-intensity, low-frequency ultrasound. PLoS One. 2008;3:e3511.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Kubanek J, Shi J, Marsh J, Chen D, Deng C, Cui J. Ultrasound modulates ion channel currents. Sci Rep. 2016;6:24170.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

This study was supported by grants from the National Research Foundation of Korea (NRF-2017R1C1B5017159) and from the Ministry of Health and Welfare, Republic of Korea (HI18C0661).

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Correspondence to Dong-Sik Chae or Il-Kwon Kim.

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All animal experimental procedures were approved by the Institutional Animal Care and Use Committee of Catholic Kwandong University International St. Mary’s Hospital in cooperation with the Association for the Assessment and Accreditation of Laboratory Animal Care and were performed in accordance with the Guidelines and Regulations for Animal Care (No. CKU 03-2017-001).

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Song, BW., Park, JH., Kim, B. et al. A Combinational Therapy of Articular Cartilage Defects: Rapid and Effective Regeneration by Using Low-Intensity Focused Ultrasound After Adipose Tissue-Derived Stem Cell Transplantation. Tissue Eng Regen Med 17, 313–322 (2020). https://doi.org/10.1007/s13770-020-00256-6

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