Transient and persistent increases in protein phosphatase activity during long-term depression in the adult hippocampus in vivo

E. Thiels, E. D. Norman, G. Barrionuevo, Eric Klann

Research output: Contribution to journalArticle

Abstract

The neural substrates of learning and memory most likely involve activity-dependent long-term changes in synaptic strength, including long- term potentiation and long-term depression. A critical element in the cascade of events hypothesized to underlie such changes in synaptic function is modification of protein phosphorylation. Long-term depression is thought to involve decreases in protein phosphorylation, which could result from reduction in protein kinase activity and/or enhancement in protein phosphatase activity. We present here direct evidence that long-term depression in the hippocampus in vivo is associated with an increase in the activity of the serine/threonine phosphatases 1 and 2A. The increase in activity of phosphatase 1 was transient, whereas that of phosphatase 2A lasted >65 min after the induction of long-term depression. Blockade of long- term depression prevented the observed increases in phosphatase activity, as did selective inhibition of phosphatase 1 and 2A. Induction of long-term depression had no effect on the level of either phosphatase, which suggests that our results reflect increases in the intrinsic activity of these two enzymes. Our timings are consistent with a model of synaptic plasticity that implicates protein dephosphorylation by serine/threonine phosphatases in the early maintenance and/or expression of long-term depression of synaptic strength.

Original languageEnglish (US)
Pages (from-to)1023-1029
Number of pages7
JournalNeuroscience
Volume86
Issue number4
DOIs
StatePublished - Jun 18 1998

Fingerprint

Phosphoprotein Phosphatases
Hippocampus
Phosphoric Monoester Hydrolases
Depression
Long-Term Synaptic Depression
Phosphorylation
Neuronal Plasticity
Long-Term Potentiation
Protein Kinases
Proteins
Maintenance
Learning
Enzymes

Keywords

  • Hippocampus
  • Long-term depression
  • N- methyl-D-aspartate
  • Protein phosphatase 1
  • Protein phosphatase 2A
  • Synaptic plasticity

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Transient and persistent increases in protein phosphatase activity during long-term depression in the adult hippocampus in vivo. / Thiels, E.; Norman, E. D.; Barrionuevo, G.; Klann, Eric.

In: Neuroscience, Vol. 86, No. 4, 18.06.1998, p. 1023-1029.

Research output: Contribution to journalArticle

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AB - The neural substrates of learning and memory most likely involve activity-dependent long-term changes in synaptic strength, including long- term potentiation and long-term depression. A critical element in the cascade of events hypothesized to underlie such changes in synaptic function is modification of protein phosphorylation. Long-term depression is thought to involve decreases in protein phosphorylation, which could result from reduction in protein kinase activity and/or enhancement in protein phosphatase activity. We present here direct evidence that long-term depression in the hippocampus in vivo is associated with an increase in the activity of the serine/threonine phosphatases 1 and 2A. The increase in activity of phosphatase 1 was transient, whereas that of phosphatase 2A lasted >65 min after the induction of long-term depression. Blockade of long- term depression prevented the observed increases in phosphatase activity, as did selective inhibition of phosphatase 1 and 2A. Induction of long-term depression had no effect on the level of either phosphatase, which suggests that our results reflect increases in the intrinsic activity of these two enzymes. Our timings are consistent with a model of synaptic plasticity that implicates protein dephosphorylation by serine/threonine phosphatases in the early maintenance and/or expression of long-term depression of synaptic strength.

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