Peptide-modified alginate surfaces as a growth permissive substrate for neurite outgrowth

被引:131
作者
Dhoot, NO
Tobias, CA
Fischer, I
Wheatley, MA
机构
[1] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[2] Drexel Univ, Dept Chem Engn, Philadelphia, PA 19104 USA
[3] Drexel Univ, Coll Med, Dept Neurobiol & Anat, Philadelphia, PA 19129 USA
关键词
spinal cord repair; alginate gel; YIGSR peptide modification; growth-permissive;
D O I
10.1002/jbm.a.30103
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Different strategies are being investigated for treatment of spinal cord injuries, one of the most promising being application of neurotrophic factors, which have been shown to prevent neuronal death and stimulate regeneration of injured axons. Ex vivo gene therapy has emerged as the leading delivery method at the site of the injury, and we have shown previously that encapsulating genetically engineered fibroblasts in an immunoprotective alginate capsule can permit implantation of the factor-secreting cells without need for immunosuppression. This strategy could be greatly enhanced by providing the sprouting neurons with a permissive substrate upon which to attach and grow. We report here studies on the modification of an alginate gel surface by either coating it with laminin or by covalent attachment of YIGSR peptide. Using NB2a neuroblastoma cells, we found that native alginate elicited minimal cell attachment (similar to1.5%); however, YIGSR-alginate conjugate elicited a fivefold increase in numbers of cells attached using peptide ratios of 0.5 and 1 mg/g alginate, ranging from 9.5% of the cells at the lower ratio, to about 44% at the higher. Only a further 19% increase was obtained at an increased peptide density of 2 mg/g alginate (similar to63% over control). Laminincoated gels showed similar to60% cell attachment. However, laminin coating did not stimulate differentiation and neurite growth, whereas both numbers and lengths of outgrowths increased with increasing peptide density on peptide-modified alginate. We demonstrate here the ability of the peptide-modified alginate gels to allow adhesion of NB2a neuroblastoma cells and to promote neurite outgrowth from these cells when attached to the peptide-modified alginate surface. Also, we show that the adhesion of NB2a neuroblastoma cells and neurite outgrowth from the attached cells is a function of the peptide density on the gel surface. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:191 / 200
页数:10
相关论文
共 51 条
  • [1] In vivo performance of a new biodegradable polyester urethane system used as a nerve guidance channel
    Borkenhagen, M
    Stoll, RC
    Neuenschwander, P
    Suter, UW
    Aebischer, P
    [J]. BIOMATERIALS, 1998, 19 (23) : 2155 - 2165
  • [2] BORKENHAGEN M, 2000, J BIOMED MATER RES, V40, P392
  • [3] Chang PL, 1995, SOMATIC GENE THERAPY, P203
  • [4] Use of nonautologous microencapsulated fibroblasts in growth hormone gene therapy to improve growth of midget swine
    Cheng, WTK
    Chen, BC
    Chiou, ST
    Chen, CM
    [J]. HUMAN GENE THERAPY, 1998, 9 (14) : 1995 - 2003
  • [5] Microencapsulated Liposomes in controlled drug delivery: Strategies to modulate drug release and eliminate the burst effect
    Dhoot, NO
    Wheatley, MA
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (03) : 679 - 689
  • [6] NEUROTROPHIC FACTORS PREVENT THE DEATH OF CNS NEURONS AFTER SPINAL-CORD LESIONS IN NEWBORN RATS
    DIENER, PS
    BREGMAN, BS
    [J]. NEUROREPORT, 1994, 5 (15) : 1913 - 1917
  • [7] THE HEPARIN-BINDING DOMAIN OF LAMININ IS RESPONSIBLE FOR ITS EFFECTS ON NEURITE OUTGROWTH AND NEURONAL SURVIVAL
    EDGAR, D
    TIMPL, R
    THOENEN, H
    [J]. EMBO JOURNAL, 1984, 3 (07) : 1463 - 1468
  • [8] NONENZYMATIC GLYCOSYLATION OF LAMININ AND THE LAMININ PEPTIDE CIKVAVS INHIBITS NEURITE OUTGROWTH
    FEDEROFF, HJ
    LAWRENCE, D
    BROWNLEE, M
    [J]. DIABETES, 1993, 42 (04) : 509 - 513
  • [9] Neurite branching on deformable substrates
    Flanagan, LA
    Ju, YE
    Marg, B
    Osterfield, M
    Janmey, PA
    [J]. NEUROREPORT, 2002, 13 (18) : 2411 - 2415
  • [10] Hermanson G. T, 1996, BIOCONJUGATE TECHNIQ, P169