Calcium-induced calcium release in skeletal muscle

M Endo - Physiological reviews, 2009 - journals.physiology.org
Calcium-induced calcium release (CICR) was first discovered in skeletal muscle. CICR is
defined as Ca2+ release by the action of Ca2+ alone without the simultaneous action of …

Mammalian animal models for Duchenne muscular dystrophy

R Willmann, S Possekel, J Dubach-Powell… - Neuromuscular …, 2009 - Elsevier
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease that affects boys and
leads to early death. In the quest for new treatments that improve the quality of life and in the …

Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle

AM Bellinger, S Reiken, C Carlson, M Mongillo, X Liu… - Nature medicine, 2009 - nature.com
Duchenne muscular dystrophy is characterized by progressive muscle weakness and early
death resulting from dystrophin deficiency. Loss of dystrophin results in disruption of a large …

Checking your SOCCs and feet: the molecular mechanisms of Ca2+ entry in skeletal muscle

RT Dirksen - The Journal of physiology, 2009 - Wiley Online Library
It has long been known that skeletal muscle contraction persists in the absence of
extracellular Ca2+. Nevertheless, recent evidence indicates that multiple distinct Ca2+ entry …

Reciprocal amplification of ROS and Ca2+ signals in stressed mdx dystrophic skeletal muscle fibers

VM Shkryl, AS Martins, ND Ullrich, MC Nowycky… - … -European Journal of …, 2009 - Springer
Muscular dystrophies are among the most severe inherited muscle diseases. The genetic
defect is a mutation in the gene for dystrophin, a cytoskeletal protein which protects muscle …

Malformed mdx myofibers have normal cytoskeletal architecture yet altered EC coupling and stress-induced Ca2+ signaling

RM Lovering, L Michaelson… - American Journal of …, 2009 - journals.physiology.org
Skeletal muscle function is dependent on its highly regular structure. In studies of dystrophic
(dy/dy) mice, the proportion of malformed myofibers decreases after prolonged whole …

Pathways of abnormal stress-induced Ca2+ influx into dystrophic mdx cardiomyocytes

M Fanchaouy, E Polakova, C Jung, J Ogrodnik… - Cell calcium, 2009 - Elsevier
In Duchenne muscular dystrophy, deficiency of the cytoskeletal protein dystrophin leads to
well-described defects in skeletal muscle, but also to dilated cardiomyopathy, accounting for …

Sarcoplasmic reticulum-mitochondrial symbiosis: bidirectional signaling in skeletal muscle

AE Rossi, S Boncompagni… - Exercise and sport …, 2009 - journals.lww.com
In mammalian skeletal muscle, an intimate association between the sarcoplasmic reticulum
(SR) and mitochondria results in a symbiotic and privileged bidirectional communication …

Sarcoplasmic reticulum–mitochondrial through-space coupling in skeletal muscle

RT Dirksen - Applied Physiology, Nutrition, and Metabolism, 2009 - cdnsciencepub.com
The skeletal muscle contractile machine is fueled by both calcium and ATP. Calcium ions
activate the contractile machinery by binding to troponin C and relieving troponin …

Role of ryanodine receptor subtypes in initiation and formation of calcium sparks in arterial smooth muscle: comparison with striated muscle

K Essin, M Gollasch - BioMed Research International, 2009 - Wiley Online Library
Calcium sparks represent local, rapid, and transient calcium release events from a cluster of
ryanodine receptors (RyRs) in the sarcoplasmic reticulum. In arterial smooth muscle cells …