Skip to main content
Log in

Experimental study on self-assembly of KLD-12 peptide hydrogel and 3-D culture of MSC encapsulated within hydrogel in vitro

  • Published:
Journal of Huazhong University of Science and Technology [Medical Sciences] Aims and scope Submit manuscript

Summary

To synthesize KLD-12 peptide with sequence of AcN-KLDLKLDLKLDL-CNH2 and trigger its self-assembly in vitro, to encapsulate rabbit MSCs within peptide hydrogel for 3-D culture and to evaluate the feasibility of using it as injectable scaffold for tissue engineering of IVD. KLD-12 peptide was purified and tested with high performance liquid chromatography (HPLC) and mass spectroscopy (MS). KLD-12 peptide solutions with concentrations of 5 g/L, 2.5 g/L and 1 g/L were triggered to self-assembly with 1×PBS in vitro, and the self-assembled peptide hydrogel was morphologically observed. Atomic force microscope (AFM) was employed to examine the inner structure of self-assembled peptide hydrogel. Mesenchymal stem cells (MSCs) were encapsulated within peptide hydrogel for 3-D culture for 2 weeks. Calcein-AM/PI fluorescence staining was used to detect living and dead cells. Cell viability was observed to evaluate the bioactivity of MSCs in KLD-12 peptide hydrogel. The results of HPLC and MS showed that the relative molecular mass of KLD-12 peptide was 1467.83, with a purity quotient of 95.36%. KLD-12 peptide at 5 g/L could self-assemble to produce a hydrogel, which was structurally integral and homogeneous and was able to provide sufficient cohesion to retain the shape of hydrogel. AFM demonstrated that the self-assembly of KLD-12 peptide hydrogel was successful and the assembled material was composed of a kind of nano-fiber with a diameter of 30–40 nm and a length of hundreds of nm. Calcein-AM/PI fluorescence staining revealed that MSCs in KLD-12 peptide hydrogel grew well. Cell activity detection exhibited that the A value increased over the culture time. It is concluded that KLD-12 peptide was synthesized successfully and was able to self-assemble to produce nano-fiber hydrogel in vitro. MSCs in KLD-12 peptide hydrogel grew well and proliferated with the culture time. KLD-12 peptide hydrogel can serve as an excellent injectable material of biological scaffolds in tissue engineering of IVD.

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.

Similar content being viewed by others

References

  1. Buckwalter JA. Aging and degeneration of the human intervertebral disc. Spine, 1995,20(11):1307–1314

    PubMed  CAS  Google Scholar 

  2. Gruber HE, Hanley EN Jr. Analysis of aging and degeneration of the human intervertebral disc: Comparison of surgical specimens with normal controls. Spine, 1998, 23(7):751–757

    Article  PubMed  CAS  Google Scholar 

  3. Rannou F, Lee TS, Zhou RH, et al. Intervertebral disc degeneration: the role of the mitochondrial pathway in annulus fibrosus cell apoptosis induced by overload. Am J Pathol, 2004,164(3):915–924

    PubMed  CAS  Google Scholar 

  4. Kisiday J, Jin M, Kurz B, et al. Self-assembling peptide hydrogel fosters chondrocyte extracellular matrix production and cell division: implications for cartilage tissue repair. Proc Natl Acad Sci USA, 2002,99(15):9996–10001

    Article  PubMed  CAS  Google Scholar 

  5. Risbud MV, Albert TJ, Guttapalli A, et al. Differentiation of mesenchymal stem cells towards a nucleus pulposus-like phenotype in vitro: implications for cell-based transplantation therapy. Spine, 2004,29(23):2627–2632

    Article  PubMed  Google Scholar 

  6. Gan JC, Ducheyne P, Vresilovic EJ, et al. Intervertebral disc tissue engineering I: characterization of the nucleus pulposus. Clin Orthop Relat Res, 2003,7(411):305–314

    Article  Google Scholar 

  7. Antoniou J, Goudsouzian NM, Heathfield TF, et al. The human lumbar endplate. Evidence of changes in biosynthesis and denaturation of the extracellular matrix with growth, maturation, aging, and degeneration. Spine, 1996,21(10):1153–1161

    Article  PubMed  CAS  Google Scholar 

  8. Antoniou J, Steffen T, Nelson F, et al. The human lumbar intervertebral disc: evidence for changes in the biosynthesis and denaturation of the extracellular matrix with growth, maturation, ageing, and degeneration. J Clin Invest, 1996,98(4):996–1003

    Article  PubMed  CAS  Google Scholar 

  9. Lyons G, Eisenstein SM, Sweet MB. Biochemical changes in intervertebral disc degeneration. Biochim Biophys Acta, 1981,673(4):443–453

    PubMed  CAS  Google Scholar 

  10. Gruber HE, Ingram JA, Leslie K, et al. Cell shape and gene expression in human intervertebral disc cells: in vitro tissue engineering studies. Biotech Histochem, 2003, 78(2):109–117

    Article  PubMed  CAS  Google Scholar 

  11. Gruber HE, Hanley EN Jr. Biologic strategies for the therapy of intervertebral disc degeneration. Expert Opin Biol Ther, 2003,3(8):1209–1214

    Article  PubMed  CAS  Google Scholar 

  12. Leung VY, Chan D, Cheung KM. Regeneration of intervertebral disc by mesenchymal stem cells: potentials, limitations, and future direction. Eur Spine J, 2006,15(Suppl 3):S406–S413

    Article  PubMed  Google Scholar 

  13. Gruber HE, Fisher EC Jr, Desai B, et al. Human intervertebral disc cells from the annulus: three-dimensional culture in agarose or alginate and responsiveness to TGF-beta1. Exp Cell Res, 1997,235(1):13–21

    Article  PubMed  CAS  Google Scholar 

  14. Thonar E, An H, Masuda K. Compartmentalization of the matrix formed by nucleus pulposus and annulus fibrosus cells in alginate gel. Biochem Soc Trans, 2002;30(Pt 6): 874–878

    PubMed  CAS  Google Scholar 

  15. Chiba K, Andersson GB, Masuda K, et al. A new culture system to study the metabolism of the intervertebral disc in vitro. Spine, 1998,23(17):1821–1827

    Article  PubMed  CAS  Google Scholar 

  16. Kasra M, Goel V, Martin J, et al. Effect of dynamic hydrostatic pressure on rabbit intervertebral disc cells. J Orthop Res, 2003,21(4):597–603

    Article  PubMed  Google Scholar 

  17. Neidlinger-Wilke C, Wurtz K, Liedert A, et al. A three-dimensional collagen matrix as a suitable culture system for the comparison of cyclic strain and hydrostatic pressure effects on intervertebral disc cells. J Neurosurgery Spine, 2005,2(4):457–465

    Article  Google Scholar 

  18. Alini M, Li W, Markovic P, et al. The potential and limitations of a cell-seeded collagen/hyaluronan scaffold to engineer an intervertebral disc-like matrix. Spine, 2003,28(5):446–454

    Article  PubMed  Google Scholar 

  19. Sato M, Asazuma T, Ishihara M, et al. An experimental study of the regeneration of the intervertebral disc with an allograft of cultured annulus fibrosus cells using a tissue-engineering method. Spine, 2003,28(6):548–553

    Article  PubMed  Google Scholar 

  20. Sato M, Asazuma T, Ishihara M, et al. An atelocollagen honeycomb-shaped scaffold with a membrane seal (ACHMS-scaffold) for the culture of annulus fibrosus cells from an intervertebral disc. J Biomed Mater Res A, 2003,64(2):248–256

    Article  PubMed  Google Scholar 

  21. Sato M, Kikuchi M, Ishihara M, et al. Tissue engineering of the intervertebral disc with cultured annulus fibrosus cells using atelocollagen honeycomb-shaped scaffold with a membrane seal (ACHMS scaffold). Med Biol Eng Comput, 2003,41(3):365–371

    Article  PubMed  CAS  Google Scholar 

  22. Sebastine IM, Williams DJ. Current developments in tissue engineering of nucleus pulposus for the treatment of intervertebral disc degeneration. Conf Proc IEEE Eng Med Biol Soc, 2007,6401–6406

  23. Steck E, Bertram H, Abel R, et al. Induction of intervertebral disc-like cells from adult mesenchymal stem cells. Stem Cells, 2005,23(3):403–411

    Article  PubMed  CAS  Google Scholar 

  24. Sobajima S, Vadala G, Shimer A. Feasibility of a stem cell therapy for intervertebral disc degeneration. Spine, 2008, 8(6):888–896

    Article  Google Scholar 

  25. Le Maitre CL, Baird P, Freemont AJ, et al. An in vitro study investigation the survival and phenotype of mesenchymal stem cells following injection into nucleus pulposus tissue. Arthritis Res Ther, 2009,11(1):R20

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This project was supported by a “863” Key Project of the High Technology Research and Development Program of China (No.2006AA02A124).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sun, J., Zheng, Q. Experimental study on self-assembly of KLD-12 peptide hydrogel and 3-D culture of MSC encapsulated within hydrogel in vitro . J. Huazhong Univ. Sci. Technol. [Med. Sci.] 29, 512–516 (2009). https://doi.org/10.1007/s11596-009-0424-6

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11596-009-0424-6

Key words

Navigation