A functional role for intra-axonal protein synthesis during axonal regeneration from adult sensory neurons

被引:279
作者
Zheng, JQ
Kelly, TK
Chang, BS
Ryazantsev, S
Rajasekaran, AK
Martin, KC
Twiss, JL
机构
[1] Univ Calif Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USA
[4] Shenyang Med Coll, Dept Neuroanat, Shenyang 110001, Peoples R China
[5] Med Univ China, Shenyang 110001, Peoples R China
关键词
mRNA localization; local protein synthesis; conditioned neuron; axonal regeneration; nerve regeneration;
D O I
10.1523/JNEUROSCI.21-23-09291.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although intradendritic protein synthesis has been documented in adult neurons, the question of whether axons actively synthesize proteins remains controversial. Adult sensory neurons that are conditioned by axonal crush can rapidly extend processes in vitro by regulating the translation of existing mRNAs (Twiss et al., 2000). These regenerating processes contain axonal but not dendritic proteins. Here we show that these axonal processes of adult sensory neurons cultured after conditioning injury contain ribosomal proteins, translational initiation factors, and rRNA. Pure preparations of regenerating axons separated from the DRG cell bodies can actively synthesize proteins in vitro and contain ribosome- bound beta -actin and neurofilament mRNAs. Blocking protein synthesis in these regenerating sensory axons causes a rapid retraction of their growth cones when communication with the cell body is blocked by axotomy or colchicine treatment. These findings indicate that axons of adult mammalian neurons can synthesize proteins and suggest that, under some circumstances, intra-axonal translation contributes to structural integrity of the growth cone in regenerating axons. By immunofluorescence, translation factors, ribosomal proteins, and rRNA were also detected in motor axons of ventral spinal roots analyzed after 7 d in vivo after a peripheral axonal crush injury. Thus, adult motor neurons are also likely capable of intra-axonal protein synthesis in vivo after axonal injury.
引用
收藏
页码:9291 / 9303
页数:13
相关论文
共 92 条
[1]   Protein synthesis in axons and terminals: significance for maintenance, plasticity and regulation of phenotype - With a critique of slow transport theory [J].
Alvarez, J ;
Giuditta, A ;
Koenig, E .
PROGRESS IN NEUROBIOLOGY, 2000, 62 (01) :1-62
[2]  
Bassell GJ, 1998, J NEUROSCI, V18, P251
[3]   COORDINATE EXPRESSION OF RIBOSOMAL-PROTEIN GENES DURING XENOPUS DEVELOPMENT [J].
BAUM, EZ ;
WORMINGTON, WM .
DEVELOPMENTAL BIOLOGY, 1985, 111 (02) :488-498
[4]   Substitution of just five nucleotides at and around the transcription start site of rat beta-actin promoter is sufficient to render the resulting transcript a subject for translational control [J].
Biberman, Y ;
Meyuhas, O .
FEBS LETTERS, 1997, 405 (03) :333-336
[5]   LONG-TERM SURVIVAL OF ANUCLEATE AXONS AND ITS IMPLICATIONS FOR NERVE REGENERATION [J].
BITTNER, GD .
TRENDS IN NEUROSCIENCES, 1991, 14 (05) :188-193
[6]   AXONAL-TRANSPORT OF ACTIN - SLOW COMPONENT-B IS THE PRINCIPAL SOURCE OF ACTIN FOR THE AXON [J].
BLACK, MM ;
LASEK, RJ .
BRAIN RESEARCH, 1979, 171 (03) :401-413
[7]   SLOW COMPONENTS OF AXONAL-TRANSPORT - 2 CYTOSKELETAL NETWORKS [J].
BLACK, MM ;
LASEK, RJ .
JOURNAL OF CELL BIOLOGY, 1980, 86 (02) :616-623
[8]   Neuronal polarity: Vectorial cytoplasmic flow precedes axon formation [J].
Bradke, F ;
Dotti, CG .
NEURON, 1997, 19 (06) :1175-1186
[9]   Delivery of newly synthesized tubulin to rapidly growing distal axons of rat sympathetic neurons in compartmented cultures [J].
Campenot, RB ;
Lund, K ;
Senger, DL .
JOURNAL OF CELL BIOLOGY, 1996, 135 (03) :701-709