Olfactory ensheathing cells (OECs) and the treatment of CNS injury: advantages and possible caveats

被引:111
作者
Barnett, SC
Riddell, JS
机构
[1] Beatson Labs, Div Clin Neurosci, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Glasgow, Inst Biomed & Life Sci, Div Neurosci & Biomed Syst, Glasgow G12 8QQ, Lanark, Scotland
关键词
CNS repair; olfactory glia;
D O I
10.1111/j.1469-7580.2004.00257.x
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
One of the main research strategies to improve treatment for spinal cord injury involves the use of cell transplantation. This review looks at the advantages and possible caveats of using glial cells from the olfactory system in transplant-mediated repair. These glial cells, termed olfactory ensheathing cells (OECs), ensheath the axons of the olfactory receptor neurons. The primary olfactory system is an unusual tissue in that it can support neurogenesis throughout life. In addition, newly generated olfactory receptor neurons are able to grow into the CNS environment of the olfactory bulb tissue and reform synapses. It is thought that this unique regenerative property depends in part on the presence of OECs. OECs share some of the proper-ties of both astrocytes and Schwann cells but appear to have advantages over these and other glial cells for CNS repair. In particular, OECs are less likely to induce hypertrophy of CNS astrocytes. As well as remyelinating demyelinated axons, OEC grafts appear to promote the restoration of functions lost following a spinal cord lesion. However, much of the evidence for this is based on behavioural tests, and the mechanisms that underlie their potential benefits in transplant-mediated repair remain to be clarified.
引用
收藏
页码:57 / 67
页数:11
相关论文
共 99 条
[31]  
FRANKLIN RJM, 1997, J NEUROSCI RES, V50, P1
[32]  
FUXE K, 1991, ADV NEUROSC, V1, P1
[33]   ASTROCYTE SCHWANN-CELL INTERACTIONS IN CULTURE [J].
GHIRNIKAR, RS ;
ENG, LF .
GLIA, 1994, 11 (04) :367-377
[34]   ON PRESENCE OF PERIPHERAL-LIKE NERVOUS AND CONNECTIVE TISSUE WITHIN IRRADIATED SPINAL CORD [J].
GILMORE, SA ;
DUNCAN, D .
ANATOMICAL RECORD, 1968, 160 (04) :675-&
[35]   CELL DYNAMICS IN OLFACTORY MUCOSA [J].
GRAZIADEI, PP .
TISSUE & CELL, 1973, 5 (01) :113-131
[36]   NEUROGENESIS AND NEURON REGENERATION IN THE OLFACTORY SYSTEM OF MAMMALS .1. MORPHOLOGICAL ASPECTS OF DIFFERENTIATION AND STRUCTURAL ORGANIZATION OF THE OLFACTORY SENSORY NEURONS [J].
GRAZIADEI, PPC ;
MONTIGRAZIADEI, GA .
JOURNAL OF NEUROCYTOLOGY, 1979, 8 (01) :1-18
[37]  
GROVES A, 1999, NATURE, V362, P453
[38]   Regenerating the damaged central nervous system [J].
Horner, PJ ;
Gage, FH .
NATURE, 2000, 407 (6807) :963-970
[39]   Collagen containing neurotrophin-3 (NT-3) attracts regrowing injured corticospinal axons in the adult rat spinal cord and promotes partial functional recovery [J].
Houweling, DA ;
Lankhorst, AJ ;
Gispen, WH ;
Bär, PR ;
Joosten, EAJ .
EXPERIMENTAL NEUROLOGY, 1998, 153 (01) :49-59
[40]   Nogo-A, a potent inhibitor of neurite outgrowth and regeneration [J].
Huber, AB ;
Schwab, ME .
BIOLOGICAL CHEMISTRY, 2000, 381 (5-6) :407-419