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

Jianhua Sun , Qixin Zheng

Current Medical Science ›› 2009, Vol. 29 ›› Issue (4) : 512 -516.

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Current Medical Science ›› 2009, Vol. 29 ›› Issue (4) : 512 -516. DOI: 10.1007/s11596-009-0424-6
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Experimental study on self-assembly of KLD-12 peptide hydrogel and 3-D culture of MSC encapsulated within hydrogel in vitro

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Abstract

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.

Keywords

peptide / self-assembly / biological scaffolds / three-dimensional cell culture

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Jianhua Sun, Qixin Zheng. Experimental study on self-assembly of KLD-12 peptide hydrogel and 3-D culture of MSC encapsulated within hydrogel in vitro. Current Medical Science, 2009, 29(4): 512-516 DOI:10.1007/s11596-009-0424-6

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References

[1]

BuckwalterJ.A.. Aging and degeneration of the human intervertebral disc. Spine, 1995, 20(11): 1307-1314

[2]

GruberH.E., HanleyE.N.Jr. Analysis of aging and degeneration of the human intervertebral disc: Comparison of surgical specimens with normal controls. Spine, 1998, 23(7): 751-757

[3]

RannouF., LeeT.S., ZhouR.H., 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

[4]

KisidayJ., JinM., KurzB., 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

[5]

RisbudM.V., AlbertT.J., GuttapalliA., 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

[6]

GanJ.C., DucheyneP., VresilovicE.J., et al.. Intervertebral disc tissue engineering I: characterization of the nucleus pulposus. Clin Orthop Relat Res, 2003, 7(411): 305-314

[7]

AntoniouJ., GoudsouzianN.M., HeathfieldT.F., 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

[8]

AntoniouJ., SteffenT., NelsonF., 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

[9]

LyonsG., EisensteinS.M., SweetM.B.. Biochemical changes in intervertebral disc degeneration. Biochim Biophys Acta, 1981, 673(4): 443-453

[10]

GruberH.E., IngramJ.A., LeslieK., et al.. Cell shape and gene expression in human intervertebral disc cells: in vitro tissue engineering studies. Biotech Histochem, 2003, 78(2): 109-117

[11]

GruberH.E., HanleyE.N.Jr. Biologic strategies for the therapy of intervertebral disc degeneration. Expert Opin Biol Ther, 2003, 3(8): 1209-1214

[12]

LeungV.Y., ChanD., CheungK.M.. Regeneration of intervertebral disc by mesenchymal stem cells: potentials, limitations, and future direction. Eur Spine J, 2006, 15(Suppl3): S406-S413

[13]

GruberH.E., FisherE.C.Jr, DesaiB., 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

[14]

ThonarE., AnH., MasudaK.. Compartmentalization of the matrix formed by nucleus pulposus and annulus fibrosus cells in alginate gel. Biochem Soc Trans, 2002, 30(Pt6): 874-878

[15]

ChibaK., AnderssonG.B., MasudaK., et al.. A new culture system to study the metabolism of the intervertebral disc in vitro. Spine, 1998, 23(17): 1821-1827

[16]

KasraM., GoelV., MartinJ., et al.. Effect of dynamic hydrostatic pressure on rabbit intervertebral disc cells. J Orthop Res, 2003, 21(4): 597-603

[17]

Neidlinger-WilkeC., WurtzK., LiedertA., 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

[18]

AliniM., LiW., MarkovicP., 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

[19]

SatoM., AsazumaT., IshiharaM., 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

[20]

SatoM., AsazumaT., IshiharaM., 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

[21]

SatoM., KikuchiM., IshiharaM., 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

[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]

SteckE., BertramH., AbelR., et al.. Induction of intervertebral disc-like cells from adult mesenchymal stem cells. Stem Cells, 2005, 23(3): 403-411

[24]

SobajimaS., VadalaG., ShimerA.. Feasibility of a stem cell therapy for intervertebral disc degeneration. Spine, 2008, 8(6): 888-896

[25]

Le MaitreC.L., BairdP., FreemontA.J., 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

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