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  5. Species differences in themorphology of transverse tubule openings in cardiomyocytes
 
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Species differences in themorphology of transverse tubule openings in cardiomyocytes
File(s)
Species differences in the morphology of transverse tubule openings in cardiomyocytes.pdf (808.54 KB)
Published version
Author(s)
Rog-Zielinska, Eva Alicja
Kong, Cherrie Hei Ting
Zgierski-Johnston, Callum Michael
Verkade, Paul
Mantell, Judith
more
Type
Journal Article
Abstract
Aims
The ultrastructure of ventricular cardiomyocyte T-tubule connections with the outer cell surface (‘mouth’ regions) has been reported to differ between mice and rabbits. In mice, T-tubule mouths form convoluted narrow spaces filled with electron-dense matter that impedes diffusion between T-tubular lumen and bulk extracellular space. Here, we explore whether T-tubule mouths are also constricted in rat (another murine model used frequently for cardiac research) and whether pig and human T-tubule mouth configurations are structurally more similar to mice or rabbits.

Methods and results
We used chemically-fixed tissue and high-pressure frozen isolated cardiomyocytes to compare T-tubule mouth architecture using transmission electron microscopy and three-dimensional electron tomography. We find that rat T-tubular mouth architecture is more similar to that of rabbits than mice, lacking the marked tortuosity and electron-dense ground substance that obstructs access to deeper portions of the T-tubular system in mice. Pilot observations in larger mammals (pig, human) suggest that mouse may be the least representative animal model of T-tubule connectivity with the outer cell surface in larger mammals.

Conclusion
Rat T-tubular system architecture appears to be more similar in size and topology to larger mammals than mice. T-tubular mouth topology may contribute to differences in experimental model behaviour, underscoring the challenge of appropriate model selection for research into cell and tissue function.
Date Issued
2018-11-01
Date Acceptance
2018-10-01
Citation
Europace, 2018, 20, pp.120-124
URI
http://hdl.handle.net/10044/1/84700
URL
https://academic.oup.com/europace/article/20/suppl_3/iii120/5202173
DOI
https://www.dx.doi.org/10.1093/europace/euy245
ISSN
1099-5129
Publisher
Oxford University Press (OUP)
Start Page
120
End Page
124
Journal / Book Title
Europace
Volume
20
Copyright Statement
© The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Cardiology
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
License URL
http://creativecommons.org/licenses/by/4.0/
Sponsor
British Heart Foundation
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000454046700014&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
FS/15/3/31047
Subjects
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Cardiovascular System & Cardiology
Heart
Cardiac
Ventricular myocyte
Ultrastructure
Electron tomography
Species differences
SARCOPLASMIC-RETICULUM
ELECTRICAL-PROPERTIES
T-TUBULES
MYOCYTES
SYSTEM
ORGANIZATION
DIFFUSION
MEMBRANE
RAT
Publication Status
Published
Coverage Spatial
Ctr Computat Med Cardiol, Lugano, SWITZERLAND
Date Publish Online
2018-10-04
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