Literature DB >> 3655718

Extra calcium on shortening in barnacle muscle. Is the decrease in calcium binding related to decreased cross-bridge attachment, force, or length?

A M Gordon1, E B Ridgway.   

Abstract

Barnacle single muscle fibers were microinjected with the calcium-specific photoprotein aequorin. We have previously shown (Ridgway, E. B., and A. M. Gordon, 1984, Journal of General Physiology, 83:75-104) that when barnacle fibers are stimulated under voltage clamp and length control and allowed to shorten during the declining phase of the calcium transient, extra myoplasmic calcium is observed. The time course of the extra calcium for shortening steps at different times during the calcium transient is intermediate between those of free calcium and muscle force. Furthermore, the amplitude increases with an increased stimulus, calcium transient, and force. Therefore, the extra calcium probably comes from the activating sites on the myofilaments, possibly as a result of changes in calcium binding by the activating sites. The change in calcium binding may be due, in turn, to the change in muscle length and/or muscle force and/or cross-bridge attachment per se. In the present article, we show that the amount of the extra calcium depends on the initial muscle length, declining at shorter lengths. This suggests length-dependent calcium binding. The relation between initial length and extra calcium, however, parallels that between initial length and peak active force. The ratio of extra calcium to active force is therefore virtually independent of initial length. These data do not distinguish between a direct effect of length on calcium binding and an indirect effect owing to changes in cross-bridge attachment and force through some geometrical factor. The amount of extra calcium increases with the size of the shortening step, tending toward saturation for steps of greater than or equal to 10%. This experiment suggests that calcium binding depends on muscle force or cross-bridge attachment, not just length (if at all). There is much less extra calcium seen with shortening steps at high force when the high force results from stretch of the active muscle than when it results from increased stimulation of muscle.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1987        PMID: 3655718      PMCID: PMC2228843          DOI: 10.1085/jgp.90.3.321

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  34 in total

1.  Theoretical model for the cooperative equilibrium binding of myosin subfragment 1 to the actin-troponin-tropomyosin complex.

Authors:  T L Hill; E Eisenberg; L Greene
Journal:  Proc Natl Acad Sci U S A       Date:  1980-06       Impact factor: 11.205

2.  Muscle activation: effects of small length changes on calcium release in single fibers.

Authors:  E B Ridgeway; A M Gordon
Journal:  Science       Date:  1975-09-12       Impact factor: 47.728

3.  Tension responses to sudden length change in stimulated frog muscle fibres near slack length.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

4.  Cooperation within actin filament in vertebrate skeletal muscle.

Authors:  R D Bremel; A Weber
Journal:  Nat New Biol       Date:  1972-07-26

5.  Stretch-induced increase in activation of skinned muscle fibres by calcium.

Authors:  M Endo
Journal:  Nat New Biol       Date:  1972-06-14

Review 6.  Calcium ion and muscle contraction.

Authors:  S Ebashi; M Endo
Journal:  Prog Biophys Mol Biol       Date:  1968       Impact factor: 3.667

7.  The time course of the active state in relation to sarcomere length and movement studied in single skeletal muscle fibres of the frog.

Authors:  K A Edman; A Kiessling
Journal:  Acta Physiol Scand       Date:  1971-02

8.  The variation in isometric tension with sarcomere length in vertebrate muscle fibres.

Authors:  A M Gordon; A F Huxley; F J Julian
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

9.  Regulation of muscular contraction. Distribution of actin control and myosin control in the animal kingdom.

Authors:  W Lehman; A G Szent-Györgyi
Journal:  J Gen Physiol       Date:  1975-07       Impact factor: 4.086

10.  Length-dependent electromechanical coupling in single muscle fibers.

Authors:  A M Gordon; E B Ridgway
Journal:  J Gen Physiol       Date:  1976-12       Impact factor: 4.086

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  29 in total

1.  Influence of length on force and activation-dependent changes in troponin c structure in skinned cardiac and fast skeletal muscle.

Authors:  D A Martyn; A M Gordon
Journal:  Biophys J       Date:  2001-06       Impact factor: 4.033

2.  Increased force levels after shortening and restretching skinned cardiac muscle.

Authors:  N M De Clerck
Journal:  J Muscle Res Cell Motil       Date:  1991-04       Impact factor: 2.698

3.  Effects of PKA phosphorylation of cardiac troponin I and strong crossbridge on conformational transitions of the N-domain of cardiac troponin C in regulated thin filaments.

Authors:  Wen-Ji Dong; Jayant James Jayasundar; Jianli An; Jun Xing; Herbert C Cheung
Journal:  Biochemistry       Date:  2007-08-03       Impact factor: 3.162

4.  Physiological consequences of thin filament cooperativity for vertebrate striated muscle contraction: a theoretical study.

Authors:  Hiroyuki Iwamoto
Journal:  J Muscle Res Cell Motil       Date:  2006-02-08       Impact factor: 2.698

5.  Structural studies of interactions between cardiac troponin I and actin in regulated thin filament using Förster resonance energy transfer.

Authors:  Jun Xing; Mathivanan Chinnaraj; Zhihong Zhang; Herbert C Cheung; Wen-Ji Dong
Journal:  Biochemistry       Date:  2008-12-16       Impact factor: 3.162

6.  Effects of rapid shortening on rate of force regeneration and myoplasmic [Ca2+] in intact frog skeletal muscle fibres.

Authors:  R Vandenboom; D R Claflin; F J Julian
Journal:  J Physiol       Date:  1998-08-15       Impact factor: 5.182

7.  Sarcomere length dependence of the rate of tension redevelopment and submaximal tension in rat and rabbit skinned skeletal muscle fibres.

Authors:  K S McDonald; M R Wolff; R L Moss
Journal:  J Physiol       Date:  1997-06-15       Impact factor: 5.182

8.  Nucleotide-dependent contractile properties of Ca(2+)-activated fast and slow skeletal muscle fibers.

Authors:  P A Wahr; H C Cantor; J M Metzger
Journal:  Biophys J       Date:  1997-02       Impact factor: 4.033

9.  Regulation of fibre contraction in a rat model of myocardial ischemia.

Authors:  Young Soo Han; Ozgur Ogut
Journal:  PLoS One       Date:  2010-03-04       Impact factor: 3.240

10.  In situ time-resolved FRET reveals effects of sarcomere length on cardiac thin-filament activation.

Authors:  King-Lun Li; Daniel Rieck; R John Solaro; Wenji Dong
Journal:  Biophys J       Date:  2014-08-05       Impact factor: 4.033

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