Literature DB >> 29768046

Does partial titin degradation affect sarcomere length nonuniformities and force in active and passive myofibrils?

V Joumaa1, F Bertrand1, S Liu1, S Poscente1, W Herzog1.   

Abstract

The aim of this study was to determine the role of titin in preventing the development of sarcomere length nonuniformities following activation and after active and passive stretch by determining the effect of partial titin degradation on sarcomere length nonuniformities and force in passive and active myofibrils. Selective partial titin degradation was performed using a low dose of trypsin. Myofibrils were set at a sarcomere length of 2.4 µm and then passively stretched to sarcomere lengths of 3.4 and 4.4 µm. In the active condition, myofibrils were set at a sarcomere length of 2.8 µm, activated, and actively stretched by 1 µm/sarcomere. The extent of sarcomere length nonuniformities was calculated for each sarcomere as the absolute difference between sarcomere length and the mean sarcomere length of the myofibril. Our main finding is that partial titin degradation does not increase sarcomere length nonuniformities after passive stretch and activation compared with when titin is intact but increases the extent of sarcomere length nonuniformities after active stretch. Furthermore, when titin was partially degraded, active and passive stresses were substantially reduced. These results suggest that titin plays a crucial role in actively stretched myofibrils and is likely involved in active and passive force production.

Entities:  

Keywords:  Z-disk; active stretch; force regulation; passive stretch; sarcomere stability

Mesh:

Substances:

Year:  2018        PMID: 29768046      PMCID: PMC6171042          DOI: 10.1152/ajpcell.00183.2017

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN: 0363-6143            Impact factor:   4.249


  47 in total

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2.  Half-sarcomere dynamics in myofibrils during activation and relaxation studied by tracking fluorescent markers.

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5.  Titin-based modulation of active tension and interfilament lattice spacing in skinned rat cardiac muscle.

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Review 6.  Titin/connectin-based modulation of the Frank-Starling mechanism of the heart.

Authors:  Norio Fukuda; Henk L Granzier
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7.  Calcium binding to an elastic portion of connectin/titin filaments.

Authors:  R Tatsumi; K Maeda; A Hattori; K Takahashi
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

8.  Altered mechanical properties of titin immunoglobulin domain 27 in the presence of calcium.

Authors:  Michael M DuVall; Jessica L Gifford; Matthias Amrein; Walter Herzog
Journal:  Eur Biophys J       Date:  2012-12-07       Impact factor: 1.733

9.  Inter-sarcomere coordination in muscle revealed through individual sarcomere response to quick stretch.

Authors:  Yuta Shimamoto; Madoka Suzuki; Sergey V Mikhailenko; Kenji Yasuda; Shin'ichi Ishiwata
Journal:  Proc Natl Acad Sci U S A       Date:  2009-06-10       Impact factor: 11.205

10.  The role of sarcomere length non-uniformities in residual force enhancement of skeletal muscle myofibrils.

Authors:  Kaleena Johnston; Azim Jinha; Walter Herzog
Journal:  R Soc Open Sci       Date:  2016-03-30       Impact factor: 2.963

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  1 in total

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  1 in total

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