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Initial stages of neural regeneration in Helisoma trivolvis are dependent upon PLA sub(2) activity

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 Ca super(2+)-dependent processes...

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Bibliographic Details
Published in:Journal of neurobiology 2003-03, Vol.54 (4), p.555-565
Main Authors: Geddis, MS, Rehder, V
Format: Article
Language:English
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Summary: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 Ca super(2+)-dependent processes, but the signaling pathways activated by Ca super(2+) 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 sub(2) (PLA sub(2)), a calcium-activated enzyme, is necessary for membrane sealing in vitro. Second, PLA sub(2) activity is also required for the formation of a new growth cone after the membrane has sealed successfully. Thus, PLA sub(2) plays a dual role by affecting both growth cone formation and membrane sealing. Third, the injury-induced activation of PLA sub(2) by Ca super(2+) controls growth cone formation through the production of leukotrienes, secondary metabolites of PLA sub(2) activity. Taken together, these results suggest that the injury-induced Ca super(2+) influx acts via PLA sub(2) and leukotriene production to assure growth cone formation. These findings indicate that events that cause an inhibition of PLA sub(2) or lipoxygenases, enzymes that produce leukotrienes, could result in the inability of neurites to regenerate.
ISSN:0022-3034
DOI:10.1002/neu.10183