Enhanced skeletal muscle contraction with myosin light chain phosphorylation by a calmodulin-sensing kinase

Jeffrey W. Ryder, Kim S. Lau, Kristine E. Kamm, James T. Stull

Research output: Contribution to journalArticle

68 Citations (Scopus)

Abstract

Repetitive low frequency stimulation results in potentiation of twitch force development in fast-twitch skeletal muscle due to myosin regulatory light chain (RLC) phosphorylation by Ca2+/calmodulin (CaM)-dependent skeletal muscle myosin light chain kinase (skMLCK). We generated transgenic mice that express an skMLCK CaM biosensor in skeletal muscle to determine whether skMLCK or CaM is limiting to twitch force potentiation. Three transgenic mouse lines exhibited up to 22-fold increases in skMLCK protein expression in fast-twitch extensor digitorum longus muscle containing type IIa and IIb fibers, with comparable expressions in slow-twitch soleus muscle containing type I and IIa fibers. The high expressing lines showed a more rapid RLC phosphorylation and force potentiation in extensor digitorum longus muscle with low frequency electrical stimulation. Surprisingly, overexpression of skMLCK in soleus muscle did not recapitulate the fast-twitch potentiation response despite marked enhancement of both fast-twitch and slow-twitch RLC phosphorylation. Analysis of calmodulin binding to the biosensor showed a frequency-dependent activation to a maximal extent of 60%. Because skMLCK transgene expression is 22-fold greater than the wild-type kinase, skMLCK rather than calmodulin is normally limiting for RLC phosphorylation and twitch force potentiation. The kinase activation rate (10.6 s-1) was only 3.6-fold slower than the contraction rate, whereas the inactivation rate (2.8 s-1) was 12-fold slower than relaxation. The slower rate of kinase inactivation in vivo with repetitive contractions provides a biochemical memory via RLC phosphorylation. Importantly, RLC phosphorylation plays a prominent role in skeletal muscle force potentiation of fast-twitch type IIb but not type I or IIa fibers.

Original languageEnglish (US)
Pages (from-to)20447-20454
Number of pages8
JournalJournal of Biological Chemistry
Volume282
Issue number28
DOIs
StatePublished - Jul 13 2007

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Skeletal Muscle Myosins
Myosin-Light-Chain Kinase
Calcium-Calmodulin-Dependent Protein Kinases
Myosin Light Chains
Phosphorylation
Calmodulin
Muscle Contraction
Muscle
Skeletal Muscle
Phosphotransferases
Light
Biosensing Techniques
Biosensors
Transgenic Mice
Fibers
Chemical activation
Muscles
Transgenes
Electric Stimulation
Data storage equipment

ASJC Scopus subject areas

  • Biochemistry

Cite this

Enhanced skeletal muscle contraction with myosin light chain phosphorylation by a calmodulin-sensing kinase. / Ryder, Jeffrey W.; Lau, Kim S.; Kamm, Kristine E.; Stull, James T.

In: Journal of Biological Chemistry, Vol. 282, No. 28, 13.07.2007, p. 20447-20454.

Research output: Contribution to journalArticle

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