Medical Journals

Ca1.2 and Cav1.3 Neuronal L-type Calcium Channels: Differential Targeting and Signaling to Pcreb.

Authors:
  • Zhang Hua
  • Fu Yu
  • Altier Christophe
  • Platzer Josef
  • Surmeier D James
  • Bezprozvanny Ilya

From: Department of Physiology, UT Southwestern Medical Center at Dallas, Dallas, TX 75390, USA.

The European journal of neuroscience

  • Publish Date: May 2006
  • ISSN: 0953-816X
  • Volume: 23
  • Issue: 9
  • Pages: 2297-310
  • Medium: Print
  • Language: English
  • Citation (JAMA): Zhang Hua, Fu Yu, Altier Christophe, et al. Ca1.2 and Cav1.3 Neuronal L-type Calcium Channels: Differential Targeting and Signaling to Pcreb.. Eur. J. Neurosci. May 2006;23:2297-310

Abstract

Neurons express multiple types of voltage-gated calcium (Ca2+) channels. Two subtypes of neuronal L-type Ca2+ channels are encoded by CaV1.2 and CaV1.3 pore-forming subunits. To compare targeting of CaV1.2 and CaV1.3 L-type Ca2+ channels, we transfected rat hippocampal neuronal cultures with surface-epitope-tagged sHA-CaV1.2 or sHA-CaV1.3a constructs and found that: (i) both sHA-CaV1.2 and sHA-CaV1.3a form clusters on the neuronal plasma membrane surface; (ii) when compared with sHA-CaV1.2 surface clusters, the sHA-CaV1.3a surface clusters were 10% larger and 25% brighter, but 35% less abundant; (iii) 81% of sHA-CaV1.2 surface clusters, but only 48% of sHA-CaV1.3a surface clusters, co-localized with synapsin clusters; (iv) co-expression with GFP-Shank-1B had no significant effect on sHA-CaV1.2 surface clusters, but promoted formation and synaptic localization of sHA-CaV1.3a surface clusters. In experiments with dihydropyridine-resistant CaV1.2 and CaV1.3a mutants we demonstrated that CaV1.3a L-type Ca2+ channels preferentially mediate nuclear pCREB signaling in hippocampal neurons at low, but not at high, levels of stimulation. In experiments with primary neuronal cultures from CaV1.3 knockout mice we discovered that CaV1.3 channels play a more important role in pCREB signaling in striatal medium spiny neurons than in hippocampal neurons. Our results provide novel insights into the function of CaV1.2 and CaV1.3 L-type Ca2+ channels in the brain.

Mesh Headings (Keywords): Animals, CREB-Binding Protein, Calcium, Calcium Channels, Calcium Channels, L-Type, Cells, Cultured, Embryo, Mammalian, Embryo, Nonmammalian, Gene Expression, Green Fluorescent Proteins, Hippocampus, Immunohistochemistry, Mice, Mice, Knockout, Models, Molecular, Mutagenesis, Neurons, Oocytes, Protein Structure, Tertiary, Rats, Signal Transduction, Synapsins, Xenopus


Check for Full Text / PubMed Unique Identifier (PMID): 16706838


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.