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Induction of chondrogenesis of human placenta-derived mesenchymal stem cells via heparin-grafted human fibroblast derived matrix

  • Noh, Yong Kwan (Center for Biomaterials, Korea Institute of Science and Technology) ;
  • Du, Ping (Center for Biomaterials, Korea Institute of Science and Technology) ;
  • Costa, Avelino Dos Santos Da (Center for Biomaterials, Korea Institute of Science and Technology) ;
  • Park, Kwideok (Center for Biomaterials, Korea Institute of Science and Technology)
  • Received : 2018.02.01
  • Accepted : 2018.03.20
  • Published : 2018.06.01

Abstract

Background: Formation of mature and functional articular cartilage is still challenging in cartilage tissue engineering. This study investigates the potential of using heparin-grafted decellularized extracellular matrix (ECM) as a novel growth factor delivery platform towards human placenta-derived mesenchymal stem cells (hPMSCs) chondrogenic differentiation. Human fibroblast-derived extracellular matrix (hFDM) is naturally obtained from in vitro-cultured human lung fibroblasts via a mild decellularization process. hFDM was then conjugated with heparin via N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) chemistry and subject to transforming growth factor (TGF)-${\beta}1$ immobilization. Once heparin grafted-hFDM (hFDM-hep) and hPMSCs were co-embedded into collagen gel, they were examined for in vitro and in vivo chondrogenesis of hPMSCs for 4 weeks. Results: We identified heparin moieties on hFDM via toluidine blue O assay and Fourier transform infrared spectroscopy, respectively. We found out that collagen spheroids containing hFDM-hep and TGF-${\beta}1$ exhibited a sustained release of growth factor for 28 days in vitro. Chondrogenesis of hPMSCs in vitro was supported by accumulated glycosaminoglycan (GAG) content and upregulated chondrogenic specific markers (collagen II, aggrecan, Sox9). Meanwhile, PKH26 - labeled hPMSCs incorporated collagen with either hFDM or hFDM-hep was pre-conditioned in a chondrogenic media for 3 days and subcutaneously implanted in the back of nude mice for 4 weeks. The implanted collagen spheroids containing both hPMSCs and hFDM-hep retained more viable hPMSCs and showed higher level of chondrogenic differentiation, based on immunostaining of collagen type II over collagen alone or Col/hFDM group. In addition, histological examination showed more positive signals of GAG via Safranin-O staining. Conclusion: TGF-${\beta}1$-immobilized hFDM-hep can provide an appropriate microenvironment for chondrogenic differentiation of hPMSCs in 3D collagen spheroid.

Keywords

Acknowledgement

Supported by : Korea Health Industry Development Institute (KHIDI)

References

  1. Martel-Pelletier J, Barr AJ, Cicuttini FM, Conaghan PG, Cooper C, Goldring MB, et al. Osteoarthritis. Nat Rev Dis Primers. 2016;10:16072.
  2. Iwasa J, Engebretsen L, Shima Y, Ochi M. Clinical application of scaffolds for cartilage tissue engineering. Knee Surg Sports Traumatol Arthrosc. 2009;17:561-77. https://doi.org/10.1007/s00167-008-0663-2
  3. Getgood A, Brooks R, Fortier L, Rushton N. Articular cartilage tissue engineering: today's research, tomorrow's practice? J Bone Joint Surg Br. 2009;91:565-76.
  4. Cucchiarini M, Madry H, Guilak F, Saris DB, Stoddart MJ, Koon Wong M, et al. A vision on the future of articular cartilage repair. Eur Cell Mater. 2014;27:12-6.
  5. Place ES, Evans ND, Stevens MM. Complexity in biomaterials for tissue engineering. Nat Mater. 2009;8:457-70. https://doi.org/10.1038/nmat2441
  6. Dvir T, Timko BP, Kohane DS, Langer R. Nanotechnological strategies for engineering complex tissues. Nat Nanotechnol. 2011;6:13-22. https://doi.org/10.1038/nnano.2010.246
  7. Huey DJ, Hu JC, Athanasiou KA. Unlike bone, cartilage regeneration remains elusive. Science. 2012;338:917-21. https://doi.org/10.1126/science.1222454
  8. Mano JF, Silva GA, Azevedo HS, Malafaya PB, Sousa RA, Silva SS, et al. Natural origin biodegradable systems in tissue engineering and regenerative medicine: present status and some moving trends. J Royal Soc Interface. 2007;4:999-1030. https://doi.org/10.1098/rsif.2007.0220
  9. Watt FM, Huck WTS. Role of the extracellular matrix in regulating stem cell fate. Nat Rev Mol Cell Biol. 2013;14:467-73. https://doi.org/10.1038/nrm3620
  10. Frantz C, Stewart KM, Weaver VM. The extracellular matrix at a glance. J Cell Sci. 2010;123:4195-200. https://doi.org/10.1242/jcs.023820
  11. Hoshiba T, Lu H, Kawazoe N, Chen G. Decellularized matrices for tissue engineering. Expert Opin Biol Ther. 2010;10:1717-28. https://doi.org/10.1517/14712598.2010.534079
  12. Fitzpatrick LE, McDevitt TC. Cell-derived matrices for tissue engineering and regenerative medicine applications. Biomater Sci. 2015;3:12-24. https://doi.org/10.1039/C4BM00246F
  13. Jeon J, Lee MS and Yang HS. Differentiated osteoblasts derived decellularized extracellular matrix to promote osteogenic differentiation. Biomater Res. 2018;22:4. https://doi.org/10.1186/s40824-018-0115-0
  14. Cen L, Liu W, Cui L, Zhang W, Cao Y. Collagen tissue engineering: development of novel biomaterials and applications. Pediatr Res. 2008;63:492-6. https://doi.org/10.1203/PDR.0b013e31816c5bc3
  15. Dhandayuthapani B, Yoshida Y, Maekawa T, Kumar DS. Polymeric scaffolds in tissue engineering application: a review. Inter J Polymer Sci. 2011;290602:19.
  16. Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, Mosca JD, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284:143-7. https://doi.org/10.1126/science.284.5411.143
  17. Cho H, Lee A and Kim K. The effect of serum types on Chondrogenic differentiation of adipose-derived stem cells. Biomater Res. 2018;22:6. https://doi.org/10.1186/s40824-018-0116-z
  18. Si YL, Zhao YL, Hao HJ, Fu XB, Han WD. MSCs: biological characteristics, clinical applications and their outstanding concerns. Ageing Res Rev. 2011;10:93-103. https://doi.org/10.1016/j.arr.2010.08.005
  19. Bobis S, Jarocha D, Majka M. Mesenchymal stem cells: characteristics and clinical applications. Folia Histochem Cytobiol. 2006;44:215-30.
  20. Vellasamy S, Sandrasaigaran P, Vidyadaran S, George E, Ramasamy R. Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue. World J Stem Cells. 2012;4:53-61. https://doi.org/10.4252/wjsc.v4.i6.53
  21. Parolini O, Caruso M. Review: preclinical studies on placenta-derived cells and amniotic membrane: an update. Placenta. 2011;25:S186-95.
  22. Kim IG, Hwang MP, Du P, Ko J, Ha C, Do SH, Park K. Bioactive cell-derived matrices combined with polymer mesh scaffold for osteogenesis and bone healing. Biomaterials. 2015;50:75-86. https://doi.org/10.1016/j.biomaterials.2015.01.054
  23. Kim IG, Ko J, Lee HR, Do SH, Park K. Mesenchymal cells condensation-inducible mesh scaffolds for cartilage tissue engineering. Biomaterials. 2016;85:18-29. https://doi.org/10.1016/j.biomaterials.2016.01.048
  24. Chung HJ, Kim HK, Yoon JJ, Park TG. Heparin immobilized porous PLGA microspheres for angiogenic growth factor delivery. Pharm Res. 2006;23:1835-41. https://doi.org/10.1007/s11095-006-9039-9
  25. Du P, Hwang MP, Noh YK, Subbiah R, Kim IG, Bae SE, Park K. Fibroblastderived matrix (FDM) as a novel vascular endothelial growth factor delivery platform. J Control Release. 2014;194:122-9. https://doi.org/10.1016/j.jconrel.2014.08.026
  26. Zhen G, Cao X. Targeting $TGF{\beta}$ signaling in subchondral bone and articular cartilage homeostasis. Trends Pharmacol Sci. 2014;35:227-36. https://doi.org/10.1016/j.tips.2014.03.005
  27. Grimaud E, Heymann D, Redini F. Recent advances in TGF-beta effects on chondrocyte metabolism: potential therapeutic roles of TGF-beta in cartilage disorders. Cytokine Growth Factor Rev. 2002;13:241-57. https://doi.org/10.1016/S1359-6101(02)00004-7
  28. Kim M, Kim SE, Kang SS, Kim YH, Tae G. The use of de-differentiated chondrocytes delivered by a heparin-based hydrogel to regenerate cartilage in partial-thickness defects. Biomaterials. 2011;32:7883-96. https://doi.org/10.1016/j.biomaterials.2011.07.015
  29. Brown G, Lim KS, Farrugia BL, Hooper GJ, Woodfield T. Covalent incorporation of heparin improves chondrogenesis in photocurable gelatin-methacryloyl hydrogels. Macromol Biosci. 2017;17:1700158. https://doi.org/10.1002/mabi.201700158

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