Literature DB >> 19250668

Distribution patterns of the Na+-Ca2+ exchanger and caveolin-3 in developing rabbit cardiomyocytes.

Eric Lin1, Vivian H Y Hung, Haruyo Kashihara, Pauline Dan, Glen F Tibbits.   

Abstract

In adult cardiac cells the established mechanism of excitation-contraction coupling is by calcium-induced calcium release (CICR) mediated by L-type Ca(2+) channels. However, in neonate cardiomyocytes, a CICR modality involving reverse mode Na(+)-Ca(2+) exchanger (NCX) activity predominates. This has been hypothesized to be due, in part, to the high expression levels of NCX in the neonate heart which drop several fold during ontogeny. Very little is known about the nature of NCX distribution within the cardiomyocyte and how this might change with development given the significant differences in gene expression. We investigated the spatial arrangements of NCX in developing rabbit ventricular myocytes with traditional as well as novel image processing and analysis techniques. Using image segmentation, colocalization analysis was conducted at the whole cell, compartmental (cell periphery and cell interior) and object levels. Because NCX has been suggested to colocalize with caveolin-3 (cav-3) and perhaps form a signaling unit within caveolae, the spatial relationship of NCX relative to cav-3 was also examined in detail. NCX and cav-3 objects were found to be isolated islands of lit voxels that are present after thresholding. These objects were categorized into non-colocalized (0%), lowly colocalized (<50%) and highly colocalized (>50%) subpopulations in both the interior and peripheral compartments. Our results show that NCX and cav-3 are distributed on the peripheral membrane as discrete objects and are not highly colocalized throughout development. 3D distance analysis revealed that NCX and cav-3 objects are organized with a longitudinal and lateral periodicity of about 1mum and that NCX and cav-3 cluster appear to be mutually exclusive on the cell periphery. We conclude that despite the very significant decrease in NCX expression with maturation, qualitatively there were no differences in NCX surface distribution or in the spatial relationship to caveolin 3.

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Year:  2009        PMID: 19250668     DOI: 10.1016/j.ceca.2009.01.001

Source DB:  PubMed          Journal:  Cell Calcium        ISSN: 0143-4160            Impact factor:   6.817


  4 in total

1.  Organization of ryanodine receptors, transverse tubules, and sodium-calcium exchanger in rat myocytes.

Authors:  Isuru D Jayasinghe; Mark B Cannell; Christian Soeller
Journal:  Biophys J       Date:  2009-11-18       Impact factor: 4.033

2.  Couplons in rat atria form distinct subgroups defined by their molecular partners.

Authors:  Meredith N Schulson; David R L Scriven; Patrick Fletcher; Edwin D W Moore
Journal:  J Cell Sci       Date:  2011-03-08       Impact factor: 5.285

3.  Detection of caveolin-3/caveolin-1/P2X7R complexes in mice atrial cardiomyocytes in vivo and in vitro.

Authors:  Claudia Pfleger; Georg Ebeling; Robert Bläsche; Miranda Patton; Hemal H Patel; Michael Kasper; Kathrin Barth
Journal:  Histochem Cell Biol       Date:  2012-05-15       Impact factor: 4.304

4.  Modeling effects of L-type ca(2+) current and na(+)-ca(2+) exchanger on ca(2+) trigger flux in rabbit myocytes with realistic T-tubule geometries.

Authors:  Peter M Kekenes-Huskey; Yuhui Cheng; Johan E Hake; Frank B Sachse; John H Bridge; Michael J Holst; J Andrew McCammon; Andrew D McCulloch; Anushka P Michailova
Journal:  Front Physiol       Date:  2012-09-10       Impact factor: 4.566

  4 in total

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