A biomaterials approach to peripheral nerve regeneration: bridging the peripheral nerve gap and enhancing functional recovery

被引:447
作者
Daly, W. [1 ]
Yao, L. [1 ]
Zeugolis, D. [1 ]
Windebank, A. [2 ]
Pandit, A. [1 ]
机构
[1] Natl Univ Ireland, Network Excellence Funct Biomat NFB, Galway, Ireland
[2] Mayo Clin, Rochester, MA USA
基金
爱尔兰科学基金会;
关键词
peripheral nerve conduit; topographical guidance; molecular therapy; Schwann cells; stem cells; neurotrophic factors; GLYCOLIC ACID) CONDUITS; MESENCHYMAL STEM-CELLS; CROSS-LINKED GELATIN; IN-VIVO EVALUATION; SCHWANN-CELLS; NEUROTROPHIC FACTOR; GROWTH-FACTOR; AXONAL REGENERATION; GUIDANCE CHANNELS; FIBRIN MATRICES;
D O I
10.1098/rsif.2011.0438
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microsurgical techniques for the treatment of large peripheral nerve injuries (such as the gold standard autograft) and its main clinically approved alternative-hollow nerve guidance conduits (NGCs)-have a number of limitations that need to be addressed. NGCs, in particular, are limited to treating a relatively short nerve gap (4 cm in length) and are often associated with poor functional recovery. Recent advances in biomaterials and tissue engineering approaches are seeking to overcome the limitations associated with these treatment methods. This review critically discusses the advances in biomaterial-based NGCs, their limitations and where future improvements may be required. Recent developments include the incorporation of topographical guidance features and/or intraluminal structures, which attempt to guide Schwann cell (SC) migration and axonal regrowth towards their distal targets. The use of such strategies requires consideration of the size and distribution of these topographical features, as well as a suitable surface for cell-material interactions. Likewise, cellular and molecular-based therapies are being considered for the creation of a more conductive nerve microenvironment. For example, hurdles associated with the short half-lives and low stability of molecular therapies are being surmounted through the use of controlled delivery systems. Similarly, cells (SCs, stem cells and genetically modified cells) are being delivered with biomaterial matrices in attempts to control their dispersion and to facilitate their incorporation within the host regeneration process. Despite recent advances in peripheral nerve repair, there are a number of key factors that need to be considered in order for these new technologies to reach the clinic.
引用
收藏
页码:202 / 221
页数:20
相关论文
共 128 条
[1]   Nano-textured self-assembled aligned collagen hydrogels promote directional neurite guidance and overcome inhibition by myelin associated glycoprotein [J].
Abu-Rub, Mohammad T. ;
Billiar, Kristen L. ;
van Es, Maarten H. ;
Knight, Andrew ;
Rodriguez, Brian J. ;
Zeugolis, Dimitrios I. ;
McMahon, Siobhan ;
Windebank, Anthony J. ;
Pandit, Abhay .
SOFT MATTER, 2011, 7 (06) :2770-2781
[2]   Functional recovery after peripheral nerve injury and implantation of a collagen guide [J].
Alluin, Olivier ;
Wittmann, Catherine ;
Marqueste, Tanguy ;
Chabas, Jean-Francois ;
Garcia, Stephane ;
Lavaut, Marie-Noelle ;
Guinard, Didier ;
Feron, Francois ;
Decherchi, Patrick .
BIOMATERIALS, 2009, 30 (03) :363-373
[3]   ECM molecules mediate both Schwann cell proliferation and activation to enhance neurite outgrowth [J].
Armstrong, Stephanie J. ;
Wiberg, Mikael ;
Terenghi, Giorgio ;
Kingham, Paul J. .
TISSUE ENGINEERING, 2007, 13 (12) :2863-2870
[4]   Glial cell line-derived neurotrophic factor released by synthetic guidance channels promotes facial nerve regeneration in the rat [J].
Barras, FM ;
Pasche, P ;
Bouche, N ;
Aebischer, P ;
Zurn, AD .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 70 (06) :746-755
[5]   Peripheral nerve regeneration through guidance tubes [J].
Belkas, JS ;
Shoichett, MS ;
Midha, R .
NEUROLOGICAL RESEARCH, 2004, 26 (02) :151-160
[6]   Peripheral nerve regeneration: An opinion on channels, scaffolds and anisotropy [J].
Bellamkonda, RV .
BIOMATERIALS, 2006, 27 (19) :3515-3518
[7]   Novel changes in gene expression following axotomy of a sympathetic ganglion: A microarray analysis [J].
Boeshore, KL ;
Schreiber, RC ;
Vaccariello, SA ;
Sachs, HH ;
Salazar, R ;
Lee, J ;
Ratan, RR ;
Leahy, P ;
Zigmond, RE .
JOURNAL OF NEUROBIOLOGY, 2004, 59 (02) :216-235
[8]   Gene expression profiling reveals that peripheral nerve regeneration is a consequence of both novel injury-dependent and reactivated developmental processes [J].
Bosse, F ;
Hasenpusch-Theil, K ;
Küry, P ;
Müller, HW .
JOURNAL OF NEUROCHEMISTRY, 2006, 96 (05) :1441-1457
[9]   In vitro cell alignment obtained with a Schwann cell enriched microstructured nerve guide with longitudinal guidance channels [J].
Bozkurt, Ahmet ;
Deumens, Ronald ;
Beckmann, Christina ;
Damink, Leon Olde ;
Schuegner, Frank ;
Heschel, Ingo ;
Sellhaus, Bernd ;
Weis, Joachim ;
Jahnen-Dechent, Wilhelm ;
Brook, Gary A. ;
Pallua, Norbert .
BIOMATERIALS, 2009, 30 (02) :169-179
[10]   Repair of motor nerve gaps with sensory nerve inhibits regeneration in rats [J].
Brenner, Michael J. ;
Hess, Jason R. ;
Myckatyn, Terence M. ;
Hayashi, Ayato ;
Hunter, Daniel A. ;
Mackinnon, Susan E. .
LARYNGOSCOPE, 2006, 116 (09) :1685-1692