The free cytosolic Ca2+ concentration ([Ca2+]i) in the dystrophin-lacking smooth muscle from mdx mice was studied to gain new insights into the relation between dystrophin and cytoplasmic Ca2+ homeostasis, which was reported to be impaired in the mdx skeletal muscle. We observed that [Ca2+]i, as measured with the fluorescent Ca2+ indicator fura-2, was not elevated in resting smooth muscle of the vas deferens from mdx mice, in comparison with control C57 mice. Changes of the external Ca2+ concentration evoked similar changes of [Ca2+]i in mdx and control vas deferens. During contraction, cytosolic Ca2+ transients were identical, both in amplitude and in kinetics, whether or not dystrophin was present. Stretches evoked similar Ca2+ increases ...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
Skeletal muscles of the mdx mouse lack dystrophin offering the possibility to study the role of intr...
The pathogenesis of Duchenne muscular dystrophy (DMD), characterised by lack of the cytoskeletal pro...
In the mdx mouse model of Duchenne muscular dystrophy, the lack of dystrophin is associated with inc...
The hypothesis that intracellular Ca2+ is elevated in dystrophic (mdx) skeletal muscle due to increa...
In the mdx mouse model of Duchenne muscular dystrophy, the lack of dystrophin is associated with inc...
The fluorescent probe Fura-2/AM was used to determine cytosolic free calcium concentration in soleus...
New Findings: What is the central question of this study? What are the early effects of dystrophin d...
1. Duchenne muscular dystrophy (DMD) is a lethal, degenerative muscle disease caused by a genetic mu...
In this study, we have tested the hypothesis that augmented [Ca(2+)] in subcellular regions or organ...
Although the reduction in dystrophin-associated glycoproteins is the primary pathophysiological cons...
Store-operated Ca entry (SOCE) is an important mechanism in virtually all cells. In adult skeletal m...
Defective expression of dystrophin in muscle cells is the primary feature of Duchenne muscular dystr...
Chronic exercise in vivo aggravates dystrophy in mdx mice. Calcium homeostasis was evaluated ex vivo...
Calcium is the most ubiquitous second messenger. Its concentration inside the cell is tightly regula...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
Skeletal muscles of the mdx mouse lack dystrophin offering the possibility to study the role of intr...
The pathogenesis of Duchenne muscular dystrophy (DMD), characterised by lack of the cytoskeletal pro...
In the mdx mouse model of Duchenne muscular dystrophy, the lack of dystrophin is associated with inc...
The hypothesis that intracellular Ca2+ is elevated in dystrophic (mdx) skeletal muscle due to increa...
In the mdx mouse model of Duchenne muscular dystrophy, the lack of dystrophin is associated with inc...
The fluorescent probe Fura-2/AM was used to determine cytosolic free calcium concentration in soleus...
New Findings: What is the central question of this study? What are the early effects of dystrophin d...
1. Duchenne muscular dystrophy (DMD) is a lethal, degenerative muscle disease caused by a genetic mu...
In this study, we have tested the hypothesis that augmented [Ca(2+)] in subcellular regions or organ...
Although the reduction in dystrophin-associated glycoproteins is the primary pathophysiological cons...
Store-operated Ca entry (SOCE) is an important mechanism in virtually all cells. In adult skeletal m...
Defective expression of dystrophin in muscle cells is the primary feature of Duchenne muscular dystr...
Chronic exercise in vivo aggravates dystrophy in mdx mice. Calcium homeostasis was evaluated ex vivo...
Calcium is the most ubiquitous second messenger. Its concentration inside the cell is tightly regula...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
Skeletal muscles of the mdx mouse lack dystrophin offering the possibility to study the role of intr...
The pathogenesis of Duchenne muscular dystrophy (DMD), characterised by lack of the cytoskeletal pro...