Axon and Schwann cell partnership during nerve regrowth

被引:151
作者
Chen, YY [1 ]
McDonald, D [1 ]
Cheng, C [1 ]
Magnowski, B [1 ]
Durand, J [1 ]
Zochodne, DW [1 ]
机构
[1] Univ Calgary, Dept Clin Neurosci, Calgary, AB T2N 4N1, Canada
关键词
laminin; peripheral nerve; peripheral nerve transection; regeneration; Schwann cell prolileration;
D O I
10.1097/01.jnen.0000171650.94341.46
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Regeneration of peripheral nerve involves an essential contribution by Schwann cells (SCs) in collaboration with regrowing axons. We examined such collaboration between new axons and Schwann cells destined to reform peripheral nerve trucks in a regeneration chamber bridging transected rat sciatic nerves. There was a highly intimate "dance" between axons that followed outgrowing and proliferating SCs. Axons without SCs only grew short distances and almost all axon processes had associated SC processes. When regeneration chambers were infused through an external access port with local mitomycin, a mitosis inhibitor, SC proliferation, migration and subsequent axon regrowth were dramatically reduced. Adding laminin to mitomycin did not reverse this regenerative lag and indicated that SCs provide more than laminin synthesis alone. Laminin infused alone supplemented endogenous laminin and facilitated first SC then axon regrowth. "Wrong way" misdirected axons were associated with misdirected SC processes and were more numerous in bridges exposed to mitomycin, but were fewer in laminin supplemented bridges. Later, by 21 days, there was myelinated axon repopulation of regenerative bridges but those exposed to mitomycin alone at early time points had substantial impairments in axon investment. Reforming peripheral nerve trucks involves a very close and intimate relationship between axons and SCs that must proliferate and migrate, facilitated by laminin.
引用
收藏
页码:613 / 622
页数:10
相关论文
共 45 条
[1]  
Bisby Mark A., 1995, P553
[2]   GDNF IS AN AGE-SPECIFIC SURVIVAL FACTOR FOR SENSORY AND AUTONOMIC NEURONS [J].
BUJBELLO, A ;
BUCHMAN, VL ;
HORTON, A ;
ROSENTHAL, A ;
DAVIES, AM .
NEURON, 1995, 15 (04) :821-828
[3]   Neuregulin and ErbB receptor signaling pathways in the nervous system [J].
Buonanno, A ;
Fischbach, GD .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :287-296
[4]  
Carroll SL, 1997, J NEUROSCI, V17, P1642
[5]   LEUKEMIA INHIBITORY FACTOR RESCUES MOTONEURONS FROM AXOTOMY-INDUCED CELL-DEATH [J].
CHEEMA, SS ;
RICHARDS, LJ ;
MURPHY, M ;
BARTLETT, PF .
NEUROREPORT, 1994, 5 (08) :989-992
[6]   In vivo proliferation, migration and phenotypic changes of Schwann cells in the presence of myelinated fibers [J].
Cheng, C ;
Zochodne, DW .
NEUROSCIENCE, 2002, 115 (01) :321-329
[7]   CALCITONIN-GENE-RELATED PEPTIDE PROMOTES SCHWANN-CELL PROLIFERATION [J].
CHENG, L ;
KHAN, M ;
MUDGE, AW .
JOURNAL OF CELL BIOLOGY, 1995, 129 (03) :789-796
[8]   GAP-43 IS EXPRESSED BY NONMYELIN-FORMING SCHWANN-CELLS OF THE PERIPHERAL NERVOUS-SYSTEM [J].
CURTIS, R ;
STEWART, HJS ;
HALL, SM ;
WILKIN, GP ;
MIRSKY, R ;
JESSEN, KR .
JOURNAL OF CELL BIOLOGY, 1992, 116 (06) :1455-1464
[9]   The cellular and molecular basis of peripheral nerve regeneration [J].
Fu, SY ;
Gordon, T .
MOLECULAR NEUROBIOLOGY, 1997, 14 (1-2) :67-116
[10]   Semaphorin-neuropilin-1 interactions in plasticity and regeneration of adult neurons [J].
Gavazzi, I .
CELL AND TISSUE RESEARCH, 2001, 305 (02) :275-284