Medical Journals

Presynaptic Plasma Membrane Ca2+ Atpase Isoform 2a Regulates Excitatory Synaptic Transmission in Rat Hippocampal Ca3.

Authors:
  • Jensen Thomas P
  • Filoteo Adelaida G
  • Knopfel Thomas
  • Empson Ruth M

From: School of Biological Sciences, Royal Holloway University of London, UK.

The Journal of physiology

  • Publish Date: Feb 2007
  • ISSN: 0022-3751
  • Volume: 579
  • Issue: Pt 1
  • Pages: 85-99
  • Medium: Print
  • Language: English
  • Citation (JAMA): Jensen Thomas P, Filoteo Adelaida G, Knopfel Thomas, et al. Presynaptic Plasma Membrane Ca2+ Atpase Isoform 2a Regulates Excitatory Synaptic Transmission in Rat Hippocampal Ca3.. J. Physiol. (Lond.) Feb 2007;579:85-99

Abstract

Plasma membrane calcium ATPase isoforms (PMCAs) are expressed in a wide variety of tissues where cell-specific expression provides ample opportunity for functional diversity amongst these transporters. The PMCAs use energy derived from ATP to extrude submicromolar concentrations of intracellular Ca2+ ([Ca2+]i) out of the cell. Their high affinity for Ca2+ and the speed with which they remove [Ca2+]i depends upon splicing at their carboxy (C)-terminal site. Here we provide biochemical and functional evidence that a brain-specific, C-terminal truncated and therefore fast variant of PMCA2, PMCA2a, has a role at hippocampal CA3 synapses. PMCA2a was enriched in forebrain synaptosomes, and in hippocampal CA3 it colocalized with the presynaptic marker proteins synaptophysin and the vesicular glutamate transporter 1, but not with the postsynaptic density protein PSD-95. PMCA2a also did not colocalize with glutamic acid decarboxylase-65, a marker of GABA-ergic terminals, although it did localize to a small extent with parvalbumin-positive presumed inhibitory terminals. Pharmacological inhibition of PMCA increased the frequency but not the amplitude of mEPSCs with little effect on mIPSCs or paired-pulse depression of evoked IPSCs. However, inhibition of PMCA activity did enhance the amplitude and slowed the recovery of paired-pulse facilitation (PPF) of evoked EPSCs. These results indicated that fast PMCA2a-mediated clearance of [Ca2+]i from presynaptic excitatory terminals regulated excitatory synaptic transmission within hippocampal CA3.

Mesh Headings (Keywords): Animals, Cell Membrane, Enzyme Inhibitors, Excitatory Postsynaptic Potentials, Hippocampus, Inhibitory Postsynaptic Potentials, Isomerism, Neural Inhibition, Organ Culture Techniques, Patch-Clamp Techniques, Plasma Membrane Calcium-Transporting ATPases, Presynaptic Terminals, Rats, Rats, Wistar, Synaptosomes


Check for Full Text / PubMed Unique Identifier (PMID): 17170045


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.