Cited by 418Cardiomyopathy and Myosin StudiesMuscle Physiology and DisordersCardiovascular Function and Risk Factors

Differential expression of cardiac titin isoforms and modulation of cellular stiffness

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Cazorla, O., Freiburg, A., Helmes, M., Centner, T., McNabb, M., Wu, Y., Trombitás, K., Labeit, S. +1 more·2000·Circulation Research

Abstract

Abstract —Extension of the I-band segment of titin gives rise to part of the diastolic force of cardiac muscle. Previous studies of human cardiac titin transcripts suggested a series of differential splicing events in the I-band segment of titin leading to the so-called N2A and N2B isoform transcripts. Here we investigated titin expression at the protein level in a wide range of mammalian species. Results indicate that the myocardium coexpresses 2 distinct titin isoforms: a smaller isoform containing the N2B element only (N2B titin) and a larger isoform with both the N2B and N2A elements (N2BA titin). The expression ratio of large N2BA to small N2B titin isoforms was found to vary greatly in different species; eg, in the left ventricle the ratio is ≈0.05 in mouse and ≈1.5 in pig. Differences in the expression ratio were also found between atria and ventricles and between different layers of the ventricular wall. Immunofluorescence experiments with isoform-specific antibodies suggest that coexpression of these isoforms takes place at the single-myocyte level. The diastolic properties of single cardiac myocytes isolated from various species expressing high levels of the small (rat and mouse) or large (pig) titin isoform were studied. On average, pig myocytes are significantly less stiff than mouse and rat myocytes. Gel analysis indicates that this result cannot be explained by varying amounts of titin in mouse and pig myocardium. Rather, low stiffness of pig myocytes can be explained by its high expression level of the large isoform: the longer extensible region of this isoform results in a lower fractional extension for a given sarcomere length and hence a lower force. Implications of our findings to cardiac function are discussed.

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Crossref · 10.1161/01.res.86.1.59

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  • Human ventricles express both compliant N2BA and stiff N2B titin isoforms with a relative N2BA:N2B ratio of ~0.4-1.2.

    “Human ventricles express both compliant N2BA and stiff N2B titin isoforms with a relative N2BA:N2B ratio of ~0.4–1.2”
  • Mouse and rat predominantly express N2B titin and considerably lower N2BA titin, with N2BA:N2B ratios of ~0.05-0.25 in mouse and ~0.06-0.1 in rat.

    “Mouse and rat predominately express N2B titin and considerably lower N2BA titin isoform with N2BA:N2B ratio ranges of ~0.05–0.25 in mouse and ~0.06–0.1 in rat”
  • Both compliant N2BA and stiff N2B titin isoforms are expressed in canines (N2BA:N2B ratio ~0.6-1) and humans (ratio ~0.4-1.2).

    “Both compliant N2BA and stiff N2B isoforms are expressed in canines (N2BA:N2B ratio of ~ 0.6–1) and humans (N2BA:N2B ratio of ~0.4–1.2) (Bell, et al., 2000; Cazorla, et al., 2000; Jaber, et al., 2008; Makarenko, et al., 2004; Nagueh, et al., 2004).”
  • Both stiff N2B and compliant N2BA titin isoforms are expressed at considerable levels in swine myocardium.

    “Both stiff N2B and compliant N2BA titin isoforms are expressed at considerable levels in swine myocardium (Cazorla, et al., 2000; Chung, et al., 2011; Opitz & Linke, 2005).”
  • Swine express more N2BA isoform (N2BA:N2B ratio 1-1.5) than humans (ratio 0.4-1.2).

    “the swine expresses more N2BA isoform (N2BA:N2B ratio of 1–1.5) than humans (N2BA:N2B ratio of 0.4–1.2) (Cazorla, et al., 2000; Chung, et al., 2011; Makarenko, et al., 2004; Nagueh, et al., 2004).”

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Authors
Cazorla, O., Freiburg, A., Helmes, M., Centner, T., McNabb, M., Wu, Y., Trombitás, K., Labeit, S., & Granzier, H.
Affiliations
  • European Molecular Biology Laboratory (DE)
  • From the Department of Veterinary and Comparative Anatomy, Pharmacology and Physiology (O.C., M.H., M.M., Y.W., K.T., H.G.), Washington State University, Pullman, Wash; the Institut für Anästhesiologie und Operative Intensivmedizin (A.F., T.C., S.L.), Universitätsklinikum, Mannheim, Germany; and European Molecular Biology Laboratory (T.C., S.L.), Heidelberg, Germany.
Venue
Circulation Research
Published
2000-01-07
Volume
86
Issue
1
Pages
59-67
ISSN
  • 0009-7330 (ISSN-L)
  • 1524-4571
OpenAlex
W2114879284
Cited by
418
References
36
Citations by year
2026: 9 · 2025: 15 · 2024: 17 · 2023: 15 · 2022: 12 · 2021: 21 · 2020: 14 · 2019: 13 · 2018: 21 · 2017: 20 · 2016: 12 · 2015: 17 · 2014: 9 · 2013: 14 · 2012: 15
FWCI
14.87
Type
journal article
Language
en
Open access
Locations
  • Circulation Research (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, other-oa)
Funders
  • American Heart Association (HL62881)
  • Washington State University
  • Deutsche Forschungsgemeinschaft
  • National Heart, Lung, and Blood Institute (R01HL061497, HL-62881, R01HL062881, HL 61497)
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiomyopathy and Myosin Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
Keywords
titin isoforms, differential splicing, diastolic stiffness, cardiomyocytes, species differences, sarcomere length, myocardium
MeSH terms
Animals, Diastole, Elasticity, Fluorescent Antibody Technique, Heart, Muscle Proteins, Myocardium, Protein Kinases, Swine, Blotting, Western, Electrophoresis, Gel, Two-Dimensional, Protein Isoforms, Mice, Rats, Connectin

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