Initial stages of neural regeneration in Helisoma trivolvis are dependent upon PLA2 activity

被引:17
作者
Geddis, MS [1 ]
Rehder, V [1 ]
机构
[1] Georgia State Univ, Dept Biol, Atlanta, GA 30302 USA
来源
JOURNAL OF NEUROBIOLOGY | 2003年 / 54卷 / 04期
关键词
PLA(2); lipoxygenase; calcium; growth cone; regeneration; Helisoma trivolvis;
D O I
10.1002/neu.10183
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronal regeneration after damage to an axon tract requires the rapid sealing of the injured plasma membrane and the subsequent formation of growth cones that can lead regenerating processes to their appropriate target. Membrane sealing and growth cone formation are Ca2+-dependent processes, but the signaling pathways activated by Ca2+ to bring about these effects remain poorly understood. An in vitro injury model was employed in which neurites from identified snail neurons (Helisoma trivolvis) were transected with a glass microknife, and the formation of new growth cones from the distal portions of transected neurites was recorded at defined times after transection. This study presents three main results. First, phospholipase A(2) (PLA(2)), a calcium-activated enzyme, is necessary for membrane sealing in vitro. Second, PLA(2) activity is also required for the formation of a new growth cone after the membrane has sealed successfully. Thus, PLA(2) plays a dual role by affecting both growth cone formation and membrane sealing. Third, the injury-induced activation of PLA(2) by Ca2+ controls growth cone formation through the production of leukotrienes, secondary metabolites of PLA(2) activity. Taken together, these results suggest that the injury-induced Ca2+ influx acts via PLA(2) and leukotriene production to assure growth cone formation. These findings indicate that events that cause an inhibition of PLA(2) or lipoxygenases, enzymes that produce leukotrienes, could result in the inability of neurites to regenerate. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:555 / 565
页数:11
相关论文
共 31 条
[1]   THE COMPLEX NATURE OF INTERACTIVE NEUROREGENERATION-RELATED MOLECULES [J].
BRODKEY, JA ;
GATES, MA ;
LAYWELL, ED ;
STEINDLER, DA .
EXPERIMENTAL NEUROLOGY, 1993, 123 (02) :251-270
[2]   Thrombin-induced growth cone collapse:: Involvement of phospholipase A2 and eicosanoid generation [J].
de la Houssaye, BA ;
Mikule, K ;
Nikolic, D ;
Pfenninger, KH .
JOURNAL OF NEUROSCIENCE, 1999, 19 (24) :10843-10855
[3]  
Edstrom A, 1996, J NEUROSCI RES, V43, P183, DOI 10.1002/(SICI)1097-4547(19960115)43:2<183::AID-JNR6>3.0.CO
[4]  
2-C
[5]   RECOVERY OF MOTOR FUNCTION AFTER SPINAL-CORD INJURY - A RANDOMIZED, PLACEBO-CONTROLLED TRIAL WITH GM-1 GANGLIOSIDE [J].
GEISLER, FH ;
DORSEY, FC ;
COLEMAN, WP .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (26) :1829-1838
[6]   Real time imaging of calcium-induced localized proteolytic activity after axotomy and its relation to growth cone formation [J].
Gitler, D ;
Spira, ME .
NEURON, 1998, 20 (06) :1123-1135
[7]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[8]   Involvement of axonal phospholipase A2 activity in the outgrowth of adult mouse sensory axons in vitro [J].
Hornfelt, M ;
Ekström, PAR ;
Edström, A .
NEUROSCIENCE, 1999, 91 (04) :1539-1547
[9]   LONG-CHAIN FATTY-ACIDS ACTIVATE CALCIUM CHANNELS IN VENTRICULAR MYOCYTES [J].
HUANG, JMC ;
XIAN, H ;
BACANER, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6452-6456
[10]   AXONAL REGENERATION OF AN IDENTIFIED HELISOMA NEURON DEPENDS ON THE SITE OF AXOTOMY [J].
KRUK, PJ ;
BULLOCH, AGM .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 31 (03) :401-412