Skip to main content

Advertisement

Log in

Fabrication and cell affinity of biomimetic structured PLGA/articular cartilage ECM composite scaffold

  • Published:
Journal of Materials Science: Materials in Medicine Aims and scope Submit manuscript

Abstract

An ideal scaffold for cartilage tissue engineering should be biomimetic in not only mechanical property and biochemical composition, but also the morphological structure. In this research, we fabricated a composite scaffold with oriented structure to mimic cartilage physiological morphology, where natural nanofibrous articular cartilage extracellular matrix (ACECM) was used to mimic the biochemical composition, and synthetic PLGA was used to enhance the mechanical strength of ACECM. The composite scaffold has well oriented structure and more than 89% of porosity as well as about 107 μm of average pore diameter. The composite scaffold was compared with ACECM and PLGA scaffolds. Cell proliferation test showed that the number of MSCs in ACECM and composite scaffolds was noticeably bigger than that in PLGA scaffold, which was coincident with results of SEM observation and cell viability staining. The water absorption of ACECM and composite scaffolds were 22.1 and 10.2 times respectively, which was much higher than that of PLGA scaffolds (3.8 times). The compressive modulus of composite scaffold in hydrous status was 1.03 MPa, which was near 10 times higher than that of hydrous ACECM scaffold. The aforementioned results suggested that the composite scaffold has the potential for application in cartilage tissue engineering.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  1. Langer R, Vacanti JP. Tissue engineering. Science. 1993;260:920–6.

    Article  CAS  Google Scholar 

  2. Nerem RM, Sambanis A. Tissue engineering: from biology to biological substitutes. Tissue Eng. 1995;1:3–13.

    Article  CAS  Google Scholar 

  3. Jeong SI, Kim SY, Cho SK, Chong MS, Kim KS, Kim H, et al. Tissue-engineered vascular grafts composed of marine collagen and PLGA fibers using pulsatile perfusion bioreactors. Biomaterials. 2007;28:1115–22.

    Article  CAS  Google Scholar 

  4. Hui TY, Cheung KMC, Cheung WL, Chan D, Chan BP. In vitro chondrogenic differentiation of human mesenchymal stem cells in collagen microspheres: influence of cell seeding density and collagen concentration. Biomaterials. 2008;29:3201–12.

    Article  CAS  Google Scholar 

  5. Yamane S, Iwasaki N, Majima T, Funakoshi T, Masuko T, Harada K, et al. Feasibility of chitosan-based hyaluronic acid hybrid biomaterial for a novel scaffold in cartilage tissue engineering. Biomaterials. 2005;26:611–9.

    Article  CAS  Google Scholar 

  6. Zhang L, Ao Q, Wang AJ, Lu GY, Kong LJ, Gong YD, et al. A sandwich tubular scaffold derived from chitosan for blood vessel tissue engineering. J Biomed Mater Res Part A. 2006;77A:277–84.

    Article  CAS  Google Scholar 

  7. Wang Y, Bella E, Lee CS, Migliaresi C, Pelcastre L, Schwartz Z, et al. The synergistic effects of 3-D porous silk fibroin matrix scaffold properties and hydrodynamic environment in cartilage tissue regeneration. Biomaterials. 2010;31:4672–81.

    Article  CAS  Google Scholar 

  8. Hu J, Feng K, Liu XH, Ma PX. Chondrogenic and osteogenic differentiations of human bone marrow-derived mesenchymal stem cells on a nanofibrous scaffold with designed pore network. Biomaterials. 2009;30:5061–7.

    Article  CAS  Google Scholar 

  9. Jung Y, Park MS, Lee JW, Kim YH, Kim SH, Kim SH. Cartilage regeneration with highly-elastic three-dimensional scaffolds prepared from biodegradable poly (L-lactide -co-3-caprolactone). Biomaterials. 2008;29:4630–6.

    Article  CAS  Google Scholar 

  10. Uematsu K, Hattori K, Ishimoto Y, Yamauchi J, Habata T, Takakura Y, et al. Cartilage regeneration using mesenchymal stem cells and a three-dimensional poly lactic-glycolic acid (PLGA) scaffold. Biomaterials. 2005;26:4273–9.

    Article  CAS  Google Scholar 

  11. Wen XJ, Tresco PA. Fabrication and characterization of permeable degradable poly(D, L-lactide-co-glycolide) (PLGA) hollow fiber phase inversion membranes for use as nerve tract guidance channels. Biomaterials. 2006;27:3800–9.

    Article  CAS  Google Scholar 

  12. Richard RD, Aldor RB, Veronique M, Sandra S, Alastair F, Simon G, et al. In vivo characterization of a novel bioresorbable poly(lactide-co-glycolide) tubular foam scaffold for tissue engineering applications. J Mater Sci Mater Med. 2004;15:729–34.

    Article  Google Scholar 

  13. Liu Y, Bharadwaj S, Lee SJ, Atala A, Zhang YY. Optimization of a natural collagen scaffold to aid cell–matrix penetration for urologic tissue engineering. Biomaterials. 2009;30:3865–73.

    Article  CAS  Google Scholar 

  14. Zhao YL, Zhang S, Zhou JY, Wang JL, Zhen MC, Liu Y, et al. The development of a tissue-engineered artery using decellularized scaffold and autologous ovine mesenchymal stem cells. Biomaterials. 2010;31:296–307.

    Article  Google Scholar 

  15. Zhang XJ, Deng ZH, Wang HL, Yang ZH, Guo WH, Li Y, et al. Expansion and delivery of human fibroblasts on micronized acellular dermal matrix for skin regeneration. Biomaterials. 2009;30:2666–74.

    Article  CAS  Google Scholar 

  16. Yang Q, Peng J, Guo QY, Huang JX, Zhang L, Yao J, et al. A cartilage ECM-derived 3-D porous acellular matrix scaffold for in vivo cartilage tissue engineering with PKH26-labeled chondrogenic bone marrow-derived mesenchymal stem cells. Biomaterials. 2008;29:2378–87.

    Article  CAS  Google Scholar 

  17. Gratz KR, Wong VW, Chen AC, Fortier LA, Nixon AJ, Sah RL. Biomechanical assessment of tissue retrieved after in vivo cartilage defect repair: tensile modulus of repair tissue and integration with host cartilage. J Biomech. 2006;36:138–46.

    Article  Google Scholar 

  18. Gotterbarm T, Richter W, Jung M, Berardi Vilei S, Mainil-Varlet P, Yamashita T, et al. An in vivo study of a growth-factor enhanced, cell free, two-layered collagen–tricalcium phosphate in deep osteochondral defects. Biomaterials. 2006;27:3387–95.

    Article  CAS  Google Scholar 

  19. Lanfer B, Seib FP, Freudenberg U, Stamov D, Bley T, Bornhäuser M, et al. The growth and differentiation of mesenchymal stem and progenitor cells cultured on aligned collagen matrices. Biomaterials. 2009;30:5950–8.

    Article  CAS  Google Scholar 

  20. Lanfer B, Hermann A, Kirsch M, Freudenberg U, Reuner U, Werner C, et al. Directed growth of adult human white matter stem cell-derived neurons on aligned fibrillar collagen. Tissue Eng Part A. 2010;16:1103–13.

    Article  CAS  Google Scholar 

  21. Tan HP, Wu JD, Lao LH, Gao CY. Gelatin/chitosan/hyaluronan scaffold integrated with PLGA microspheres for cartilage tissue engineering. Acta Biomater. 2009;5:328–37.

    Article  CAS  Google Scholar 

  22. Dai WD, Kawazoe N, Lin XT, Dong J, Chen GP. The influence of structural design of PLGA/collagen hybrid scaffolds in cartilage tissue engineering. Biomaterials. 2009;30:1–12.

    Article  CAS  Google Scholar 

  23. Wu SC, Chang JK, Wang CK, Wang GJ, Ho ML. Enhancement of chondrogenesis of human adipose derived stem cells in a hyaluronan-enriched microenvironment. Biomaterials. 2010;31:631–40.

    Article  Google Scholar 

  24. Shi GX, Cai Q, Wang CY, Lu N, Wang SG, Bei JZ. Fabrication of cell scaffold of poly(L-lactic acid) and poly(L-lactic-co-glycolic acid) and biocompatibility. Polym Adv Technol. 2002;13:227–32.

    Article  CAS  Google Scholar 

  25. Yang F, Qu X, Cui WJ, Bei JZ, Yu FY, Lu SB, et al. Manufacturing and morphology structure of polylactide-type microtubules orientation structured scaffolds. Biomaterials. 2006;27:4923–33.

    Article  CAS  Google Scholar 

  26. Ma PX, Zhang RY. Microtubular architecture of biodegradable polymer scaffolds. J Biomed Mater Res. 2001;56:469–77.

    Article  CAS  Google Scholar 

  27. Yang HN, Park JS, Na K, Woo DG, Kwon YD, Park KH. The use of green fluorescence gene (GFP)-modified rabbit mesenchymal stem cells (rMSCs) co-cultured with chondrocytes in hydrogel constructs to reveal the chondrogenesis of MSCs. Biomaterials. 2009;30:6374–85.

    Article  CAS  Google Scholar 

  28. Wise JK, Yarin AL, Megaridis CM, Cho M. Chondrogenic differentiation of human mesenchymal stem cells on oriented nanofibrous scaffolds: engineering the superficial zone of articular cartilage. Tissue Eng Part A. 2009;15:913–21.

    Article  CAS  Google Scholar 

  29. Li WJ, Jiang YJ, Tuan RS. Chondrocyte phenotype in engineered fibrous matrix is regulated by fiber size. Tissue Eng. 2006;12:1775–85.

    Article  CAS  Google Scholar 

  30. Roosa SM, Kemppainen JM, Moffitt EN, Krebsbach PH, Hollister SJ. The pore size of polycaprolactone scaffolds has limited influence on bone regeneration in an in vivo model. J Biomed Mater Res A. 2010;92:359–68.

    Google Scholar 

  31. Yang F, Murugan R, Wang S, Ramakrishna S. Electrospinning of nano/micro scale poly (L-lactic acid) aligned fibers and their potential in neural tissue engineering. Biomaterials. 2005;26:2603–10.

    Article  CAS  Google Scholar 

  32. Lee M, Wu BM, Dunn JC. Effect of scaffold architecture and pore size on smooth muscle cell growth. J Biomed Mater Res A. 2008;87:1010–6.

    Google Scholar 

  33. Kasten P, Beyen I, Niemeyer P, Luginbuhl R, Bohner M, Richter W. Porosity and pore size of beta-tricalcium phosphate scaffold can influence protein production and osteogenic differentiation of human mesenchymal stem cells: an in vitro and in vivo study. Acta Biomater. 2008;4:1904–15.

    Article  CAS  Google Scholar 

  34. Campbell CE, von Recum AF. Microtopography and soft tissue response. J Invest Surg. 1989;2:51–74.

    Article  CAS  Google Scholar 

  35. Deligianni DD, Katsala ND, Koutsoukos PG. Effect of surface roughness of hydroxyapatite on human bone marrow cell adhesion, proliferation, differentiation and detachment strength. Biomaterials. 2001;22:87–96.

    Article  CAS  Google Scholar 

  36. Kuroda R, Isada K, Matsumoto T, Akisue T, Fujioka H, Mizuno K, et al. Treatment of a full-thickness articular cartilage defect in the femoral condyle of an athlete with autologous bone-marrow stromal cells. Osteoarthr Cartil. 2007;15:226–31.

    Article  CAS  Google Scholar 

  37. Wakitani S, Imoto K, Yamamoto T, Saito M, Murata N, Yoneda M, et al. Human autologous culture expanded bone marrow mesenchymal cell transplantation for repair of cartilage defects in osteoarthritis knees. Osteoarthr Cartil. 2002;10:199–206.

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This study was funded by the National Natural Science Foundation of China (30973047, 2080409), National High-Tech Research and Development Program (2005CB522704, 2007AA021902), National Science and Technology Supportive Program (2006BAI16B04).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Quanyi Guo.

Additional information

Xifu Zheng and Fei Yang contribute equally to this manuscript.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zheng, X., Yang, F., Wang, S. et al. Fabrication and cell affinity of biomimetic structured PLGA/articular cartilage ECM composite scaffold. J Mater Sci: Mater Med 22, 693–704 (2011). https://doi.org/10.1007/s10856-011-4248-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10856-011-4248-0

Keywords

Navigation