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脱细胞猪角膜基质体外支持角膜上皮和基质细胞的生长

http://www.cnophol.com 2009-3-9 16:37:50 中华眼科在线

  DISCUSSION

  The natural corneal stromas have already been used as the carrier for corneal cells in previous research, but these corneal stroma scaffolds contained cells [6,7,9]. The cell components are the source of the antigens of the major histocompatibility complex [10,11]. The natural corneal stroma containing cells is not fit for the standard of scaffold of tissue engineering cornea because of its antigens. One way to reduce the antigen and pathogenicity of the natural cornea stroma may be to remove the cell compositions in it.

  However, decellularization protocols applied on the natural corneal stroma may affect the composition and morphology of the surface of the natural materials. This may affect the cell compatibility of the material.

  Figure 1A:Phase contrast photograph shows the growth of the rabbits corneal epithelium cells on APCS at 3 days. (magnification ×200); B: The section of H&E shows the growth of the rabbits corneal epithelium cells on APCS in 23 layers at 10 days (magnification ×400); C: Phase contrast photograph shows the growth of the rabbits corneal stroma cells on APCS at 4 days (magnification ×200); D: The section of H&E shows the stroma cells invade into the interlaminar of scaffold at 5 days (magnification ×200)(略)

  In this study, to observe the effect of the rabbits corneal cells growing on APCS, we performed the experiment in vitro. The results showed cornea epithelium cells could grow and stratify on the surface of APCS without any coating. The study also suggested that the corneal stromal cells could grow on APCS and invade the interlaminar of the scaffold. This indicates that APCS can support the growth of the rabbit corneal cells in vitro. We suppose that APCS prepared by the methods in accordance with previous report [8], like other acellular biologic materials, comprise the natural corneal ECM retaining many types of cytokines and chemical signals [12]. APCS can provide the surface such as the basement membrane for the growth of corneal epithelium and the porous microenvironment for the stromal cells to invade and proliferate [8].

【参考文献】
    1 Duan D, Klenkler BJ, Sheardown H. Progress in the development of a corneal replacement: keratoprostheses and tissueengineered corneas. Expert Rev Med Devices 2006;3:5972

  2 Legeais JM, Renard GA. Second generation of artificial cornea (Biokpro II). Biomaterials 1998;19:15171522

  3 Leibowitz HM, TrinkausRandall V, Tsuk A, Franzblau C. Progress in the development of a synthetic cornea. Prog Retinal Eye Res 1994;13:605621

  4 TrinkausRandall V, Wu XY, Tablante R, Tsuk A. Implantation of a synthetic cornea: design, development and biological response. Artif Organs 1997;21:11851191

  5 Hicks CR, Chirila TV, Clayton AB, Fitton JH, Vijayasekaran S, Dalton PD, Lou X, Platten S, Ziegelaar B, Hong Y, Crawford GJ, Constable IJ. Clinical results of implantation of the Chirila keratoprosthesis in rabbits. Br J Ophthalmol 1998;82:1825

  6 Friend J, Kinoshita S, Thoft R, Eliason J. Corneal epithelial cell cultures on stromal carriers. Invest Ophthalmol Vis Sci 1982;23:4149

  7 Amano S. Transplantation of cultured human corneal endothelial cells. Cornea 2003;22:S66S74

  8 Lin XC, Hui YN, Meng H, Zhang YJ, Jin Y. The preparation and the observation of the histological structure of the acellular porcine corneal stroma. Int J Ophthalmol(Guoji Yanke Zazhi)2007;7(1):4951

  9 Amano S, Shimomura N, Kaji Y, Ishii K, Yamagami S, Araie M. Antigenicity of porcine cornea as xenograft. Curr Eye Res 2003;26:313331

  10 Hargrave SL, Mayhew E, Hegde S, Niederkorn J. Are corneal cells susceptible to antibodymediated killing in corneal allograft rejection? Transpl Immunol 2003;11:7989

  11 Wang ZC, Ge J, Xu JT, Chen JQ. Relative quantitative analysis of corneal immunogenicity. Chi J Ophthalmol 2002;38:535538

  12 Gilbert TW, Sellaro TL, Badylak SF. Decellularization of tissues and organs. Biomaterials 2006;27:36753683

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