Evaluation of cellular organization and axonal regeneration through linear PLA foam implants in acute and chronic spinal cord injury

被引:22
作者
Cai, Jie [1 ]
Ziemba, Kristine S. [1 ]
Smith, George M. [1 ]
Jin, Ying [1 ]
机构
[1] Univ Kentucky, Dept Physiol, Lexington, KY 40536 USA
关键词
poly (lactic acid); neural tissue engineering; guidance channel; axonal regeneration; spinal cord injury;
D O I
10.1002/jbm.a.31296
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There are few studies of neural implants in spinal cord injury (SCI) focused on supporting directed axon growth. In this study, we fabricated a macroporous poly (lactic acid) (PLA) foam with oriented inner channels. Amorphous foam without linear channels served as a control in an acute SCI injury model, and the effectiveness of foam with linear channels was further investigated in a chronic SCI model. Implants were placed into a 2 mm hemisection lesion cavity at the T8 spinal cord level in adult rats. Two weeks post-implantation, tissue sections including the implants were examined using antibodies against GFAP, p75, ED-1, laminin, GAP-43, and CGRP. Foam implants were well-integrated with the host spinal cord. In linear foams, numerous DAPI-stained cells were found within the inner channels. Schwann cells but not astrocytes had migrated within the channels. Intense laminin staining was observed throughout the extracellular matrix substrate. GAP-43- and CGRP-positive axons grew through the implants following the linear channels. In the amorphous control foams, DAPT staining distributed evenly through the pores. However, the growth of GAP-43 or CGRP-positive axons was misguided and impeded at the entrance area of the foam. Higher numbers of GAP-43 and CGRP-positive axons grew into linear foam implants after chronic SCI than acute SCI. These results suggest the potential application of linear foam implants in cell and axon guidance for SCI repair, especially for chronic SCI. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:512 / 520
页数:9
相关论文
共 47 条
[1]  
BIXBY JL, 1991, ANNU REV CELL BIOL, V7, P117, DOI 10.1146/annurev.cellbio.7.1.117
[2]  
Borgens RB, 2001, J NEUROSCI RES, V66, P1179
[3]   NEURAL TISSUE-TRANSPLANTS RESCUE AXOTOMIZED RUBROSPINAL CELLS FROM RETROGRADE DEATH [J].
BREGMAN, BS ;
REIER, PJ .
JOURNAL OF COMPARATIVE NEUROLOGY, 1986, 244 (01) :86-95
[4]   Permeable guidance channels containing microfilament scaffolds enhance axon growth and maturation [J].
Cai, J ;
Peng, XJ ;
Nelson, KD ;
Eberhart, R ;
Smith, GM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 75A (02) :374-386
[5]   Synergistic improvements in cell and axonal migration across sciatic nerve lesion gaps using bioresorbable filaments and heregulin-β1 [J].
Cai, J ;
Peng, XJ ;
Nelson, KD ;
Eberhart, R ;
Smith, GM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 69A (02) :247-258
[6]   The molecular structure of cell adhesion molecules [J].
Chothia, C ;
Jones, EY .
ANNUAL REVIEW OF BIOCHEMISTRY, 1997, 66 :823-862
[7]   A REVIEW AND UPDATE OF EXPERIMENT AND CLINICAL-STUDIES OF SPINAL-CORD INJURY [J].
COLLINS, WF .
PARAPLEGIA, 1983, 21 (04) :204-219
[8]   Axonal regeneration and functional recovery after complete spinal cord transection in rats by delayed treatment with transplants and neurotrophins [J].
Coumans, JV ;
Lin, TTS ;
Dai, HN ;
MacArthur, L ;
McAtee, M ;
Nash, C ;
Bregman, BS .
JOURNAL OF NEUROSCIENCE, 2001, 21 (23) :9334-9344
[9]   AXONAL ELONGATION INTO PERIPHERAL NERVOUS-SYSTEM BRIDGES AFTER CENTRAL NERVOUS-SYSTEM INJURY IN ADULT-RATS [J].
DAVID, S ;
AGUAYO, AJ .
SCIENCE, 1981, 214 (4523) :931-933
[10]   Structure of laminin substrate modulates cellular signaling for neuritogenesis [J].
Freire, E ;
Gomes, FCA ;
Linden, R ;
Neto, VM ;
Coelho-Sampaio, T .
JOURNAL OF CELL SCIENCE, 2002, 115 (24) :4867-4876