Differential regulation of phospholipase C isozymes in the rat facial nucleus following axotomy

Neuroscience. 1994 Mar;59(1):121-9. doi: 10.1016/0306-4522(94)90104-x.

Abstract

The expression of phospholipase C isozymes and phosphatidylinositol 4-kinase in the rat facial nucleus was studied using in situ hybridization at various times after unilateral crushing and resectioning the facial nerve. The level of phospholipase C alpha messenger RNA increased from three days to one week after the operation. On the other hand, an apparent reduction in the level of phospholipase C beta 1 occurred from three days to one week after resection. After either crushing or resection, phospholipase C gamma 1 messenger RNA levels were not noticeably changed. As phosphatidylinositol 4-kinase is the rate-limiting enzyme for the production of phosphatidylinositol 4,5-bisphosphate, which is the preferred substrate for phospholipase C, we investigated the expression of phosphatidylinositol 4-kinase messenger RNA. The level of phosphatidylinositol 4-kinase messenger RNA was decreased one day after axonal injury. Among phospholipase C isozymes, phospholipase C alpha is up-regulated. As the structure of phospholipase C alpha is different from other isozymes, phospholipase C alpha is supposed to have a different function. The present unique up-regulation of phospholipase C alpha may suggest a novel function in nerve regeneration. Phospholipase C beta 1 is down-regulated, as is phosphatidylinositol 4-kinase. This suggests that the signal transmission system using a G-linked receptor is broken down after nerve injury. On the other hand, phospholipase C gamma 1, which is related to the receptor tyrosine kinase, does not demonstrate any transcriptional regulation after nerve injury.

MeSH terms

  • 1-Phosphatidylinositol 4-Kinase
  • Animals
  • Axons / physiology*
  • Brain / cytology
  • Brain / physiology*
  • Denervation*
  • Facial Nerve / physiology*
  • In Situ Hybridization
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Male
  • Motor Neurons / metabolism
  • Nerve Crush
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Type C Phospholipases / genetics
  • Type C Phospholipases / metabolism*

Substances

  • Isoenzymes
  • RNA, Messenger
  • Phosphotransferases (Alcohol Group Acceptor)
  • 1-Phosphatidylinositol 4-Kinase
  • Type C Phospholipases