Influence of cross-linked hyaluronic acid hydrogels on neurite outgrowth and recovery from spinal cord injury

被引:88
作者
Horn, Eric M.
Beaumont, Michael
Shu, Xiao Zheng
Harvey, Adrian
Prestwich, Glenn D.
Horn, Kris M.
Gibson, Alan R.
Preul, Mark C.
Panitch, Alyssa
机构
[1] St Josephs Hosp, Barrow Neurol Inst, Neurosci Publicat, Div Neurol Surg, Phoenix, AZ 85013 USA
[2] St Josephs Hosp, Barrow Neurol Inst, Div Neurobiol, Phoenix, AZ 85013 USA
[3] Arizona State Univ, Harrington Dept Bioengn, Tempe, AZ USA
[4] Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
[5] Univ Utah, Ctr Therapeut Biomat, Salt Lake City, UT 84112 USA
关键词
hyaluronic acid; neural tissue engineering; neurite outgrowth; dorsal root ganglia; spinal cord transection; rat;
D O I
10.3171/spi.2007.6.2.133
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Therapies that use bioactive materials as replacement extracellular matrices may hold the potential to mitigate the inhibition of regeneration observed after central nervous system trauma. Hyaluronic acid (HA), a nonsulfated glycosaminoglycan ubiquitous in all tissues, was investigated as a potential neural tissue engineering matrix. Methods. Chick dorsal root ganglia were cultured in 3D hydrogel matrices composed of cross-linked thiol-modified HA or fibrin. Samples were cultured and images were acquired at 48-, 60-, and 192-hour time points. Images of all samples were analyzed at 48 hours of incubation to quantify the extent of neurite growth. Cultures in crosslinked thiolated HA exhibited more than a 50% increase in neurite length compared with fibrin samples. Furthermore, cross-linked thiolated HA supported neurites for the entire duration of the culture period, whereas fibrin cultures exhibited collapsed and degenerating extensions beyond 60 hours. Two concentrations of the thiolated HA (0.5 and 1%) were then placed at the site of a complete thoracic spinal cord transection in rats. The ability of the polymer to promote regeneration was tested using motor evoked potentials, retrograde axonal labeling, and behavioral assessments. There were no differences in any of the parameters between rats treated with the polymer and controls. Conclusions. The use of a cross-linked HA scaffold promoted robust neurite outgrowth. Although there was no benefit from the polymer in a rodent spinal cord injury model, the findings in this study represent an early step in the development of semisynthetic extracellular matrice scaffolds for the treatment of neuronal injury.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 47 条
[1]   Pharmacological approaches to repair the injured spinal cord [J].
Baptiste, DC ;
Fehlings, MG .
JOURNAL OF NEUROTRAUMA, 2006, 23 (3-4) :318-334
[2]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[3]  
BERRY M, 1999, CNS INJURIES CELLULA
[4]  
CHEN GH, 1996, SCIENCE, V273, P510
[5]   The use of fibrin glue in skin grafts and tissue-engineered skin replacements: A review [J].
Currie, LJ ;
Sharpe, JR ;
Martin, R .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2001, 108 (06) :1713-1726
[6]   Hyaluronan-binding proteins: Tying up the giant [J].
Day, AJ ;
Prestwich, GD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (07) :4585-4588
[7]   Hyaluronan: Its nature, distribution, functions and turnover [J].
Fraser, JRE ;
Laurent, TC ;
Laurent, UBG .
JOURNAL OF INTERNAL MEDICINE, 1997, 242 (01) :27-33
[8]   Systematic analysis of axonal damage and inflammatory response in different white matter tracts of acutely injured rat spinal cord [J].
Gomes-Leal, W ;
Corkill, DJ ;
Picanço-Diniz, CW .
BRAIN RESEARCH, 2005, 1066 (1-2) :57-70
[9]   Fast-gelling injectable blend of hyaluronan and methylcellulose for intrathecal, localized delivery to the injured spinal cord [J].
Gupta, D ;
Tator, CH ;
Shoichet, MS .
BIOMATERIALS, 2006, 27 (11) :2370-2379
[10]   In vivo engineering of the vocal fold extracellular matrix with injectable hyaluronic acid hydrogels: Early effects on tissue repair and biomechanics in a rabbit model [J].
Hansen, JK ;
Thibeault, SL ;
Walsh, JF ;
Shu, XZ ;
Prestwich, GD .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2005, 114 (09) :662-670