Intracellular Ca2+ transients in delta-sarcoglycan knockout mouse skeletal muscle

δ-Sarcoglycan (δ-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane fragility and increased Ca 2+ permeability have been linked to muscle degeneration. However, little is known about the mechanisms by which g...

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Published inBiochimica et biophysica acta Vol. 1800; no. 3; pp. 373 - 379
Main Authors Solares-Pérez, Alhondra, Sánchez, Jorge A., Zentella-Dehesa, Alejandro, García, María C., Coral-Vázquez, Ramón M.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.03.2010
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ISSN0304-4165
0006-3002
1872-8006
DOI10.1016/j.bbagen.2009.11.011

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Abstract δ-Sarcoglycan (δ-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane fragility and increased Ca 2+ permeability have been linked to muscle degeneration. However, little is known about the mechanisms by which genetic defects lead to disease. Isolated skeletal muscle fibers of wild-type and δ-SG KO mice were used to investigate whether the absence of δ-SG alters the increase in intracellular Ca 2+ during single twitches and tetani or during repeated stimulation. Immunolabeling, electrical field stimulation and Ca 2+ transient recording techniques with fluorescent indicators were used. Ca 2+ transients during single twitches and tetani generated by muscle fibers of δ-SG KO mice are similar to those of wild-type mice, but their amplitude is greatly decreased during protracted stimulation in KO compared to wild-type fibers. This impairment is independent of extracellular Ca 2+ and is mimicked in wild-type fibers by blocking store-operated calcium channels with 2-aminoethoxydiphenyl borate (2-APB). Also, immunolabeling indicates the localization of a δ-SG isoform in the sarcoplasmic reticulum of the isolated skeletal muscle fibers of wild-type animals, which may be related to the functional differences between wild-type and KO muscles. δ-SG has a role in calcium homeostasis in skeletal muscle fibers. These results support a possible role of δ-SG on calcium homeostasis. The alterations caused by the absence of δ-SG may be related to the pathogenesis of muscular dystrophy.
AbstractList delta-Sarcoglycan (delta-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane fragility and increased Ca(2+) permeability have been linked to muscle degeneration. However, little is known about the mechanisms by which genetic defects lead to disease.BACKGROUNDdelta-Sarcoglycan (delta-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane fragility and increased Ca(2+) permeability have been linked to muscle degeneration. However, little is known about the mechanisms by which genetic defects lead to disease.Isolated skeletal muscle fibers of wild-type and delta-SG KO mice were used to investigate whether the absence of delta-SG alters the increase in intracellular Ca(2+) during single twitches and tetani or during repeated stimulation. Immunolabeling, electrical field stimulation and Ca(2+) transient recording techniques with fluorescent indicators were used.METHODSIsolated skeletal muscle fibers of wild-type and delta-SG KO mice were used to investigate whether the absence of delta-SG alters the increase in intracellular Ca(2+) during single twitches and tetani or during repeated stimulation. Immunolabeling, electrical field stimulation and Ca(2+) transient recording techniques with fluorescent indicators were used.Ca(2+) transients during single twitches and tetani generated by muscle fibers of delta-SG KO mice are similar to those of wild-type mice, but their amplitude is greatly decreased during protracted stimulation in KO compared to wild-type fibers. This impairment is independent of extracellular Ca(2+) and is mimicked in wild-type fibers by blocking store-operated calcium channels with 2-aminoethoxydiphenyl borate (2-APB). Also, immunolabeling indicates the localization of a delta-SG isoform in the sarcoplasmic reticulum of the isolated skeletal muscle fibers of wild-type animals, which may be related to the functional differences between wild-type and KO muscles.RESULTSCa(2+) transients during single twitches and tetani generated by muscle fibers of delta-SG KO mice are similar to those of wild-type mice, but their amplitude is greatly decreased during protracted stimulation in KO compared to wild-type fibers. This impairment is independent of extracellular Ca(2+) and is mimicked in wild-type fibers by blocking store-operated calcium channels with 2-aminoethoxydiphenyl borate (2-APB). Also, immunolabeling indicates the localization of a delta-SG isoform in the sarcoplasmic reticulum of the isolated skeletal muscle fibers of wild-type animals, which may be related to the functional differences between wild-type and KO muscles.delta-SG has a role in calcium homeostasis in skeletal muscle fibers.CONCLUSIONSdelta-SG has a role in calcium homeostasis in skeletal muscle fibers.These results support a possible role of delta-SG on calcium homeostasis. The alterations caused by the absence of delta-SG may be related to the pathogenesis of muscular dystrophy.GENERAL SIGNIFICANCEThese results support a possible role of delta-SG on calcium homeostasis. The alterations caused by the absence of delta-SG may be related to the pathogenesis of muscular dystrophy.
delta-Sarcoglycan (delta-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane fragility and increased Ca(2+) permeability have been linked to muscle degeneration. However, little is known about the mechanisms by which genetic defects lead to disease. Isolated skeletal muscle fibers of wild-type and delta-SG KO mice were used to investigate whether the absence of delta-SG alters the increase in intracellular Ca(2+) during single twitches and tetani or during repeated stimulation. Immunolabeling, electrical field stimulation and Ca(2+) transient recording techniques with fluorescent indicators were used. Ca(2+) transients during single twitches and tetani generated by muscle fibers of delta-SG KO mice are similar to those of wild-type mice, but their amplitude is greatly decreased during protracted stimulation in KO compared to wild-type fibers. This impairment is independent of extracellular Ca(2+) and is mimicked in wild-type fibers by blocking store-operated calcium channels with 2-aminoethoxydiphenyl borate (2-APB). Also, immunolabeling indicates the localization of a delta-SG isoform in the sarcoplasmic reticulum of the isolated skeletal muscle fibers of wild-type animals, which may be related to the functional differences between wild-type and KO muscles. delta-SG has a role in calcium homeostasis in skeletal muscle fibers. These results support a possible role of delta-SG on calcium homeostasis. The alterations caused by the absence of delta-SG may be related to the pathogenesis of muscular dystrophy.
δ-Sarcoglycan (δ-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane fragility and increased Ca 2+ permeability have been linked to muscle degeneration. However, little is known about the mechanisms by which genetic defects lead to disease. Isolated skeletal muscle fibers of wild-type and δ-SG KO mice were used to investigate whether the absence of δ-SG alters the increase in intracellular Ca 2+ during single twitches and tetani or during repeated stimulation. Immunolabeling, electrical field stimulation and Ca 2+ transient recording techniques with fluorescent indicators were used. Ca 2+ transients during single twitches and tetani generated by muscle fibers of δ-SG KO mice are similar to those of wild-type mice, but their amplitude is greatly decreased during protracted stimulation in KO compared to wild-type fibers. This impairment is independent of extracellular Ca 2+ and is mimicked in wild-type fibers by blocking store-operated calcium channels with 2-aminoethoxydiphenyl borate (2-APB). Also, immunolabeling indicates the localization of a δ-SG isoform in the sarcoplasmic reticulum of the isolated skeletal muscle fibers of wild-type animals, which may be related to the functional differences between wild-type and KO muscles. δ-SG has a role in calcium homeostasis in skeletal muscle fibers. These results support a possible role of δ-SG on calcium homeostasis. The alterations caused by the absence of δ-SG may be related to the pathogenesis of muscular dystrophy.
Author Coral-Vázquez, Ramón M.
Zentella-Dehesa, Alejandro
Sánchez, Jorge A.
Solares-Pérez, Alhondra
García, María C.
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Issue 3
Keywords DGC
δ-SG
KO
Intracellular calcium
SOC
Muscle fibers
EDL
Ca 2+ transients
SG–SSPN
Muscular dystrophy
SG
Sarcoplasmic reticulum
SR
Sarcoglycan–sarcospan complex
Language English
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Snippet δ-Sarcoglycan (δ-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy. Membrane...
delta-Sarcoglycan (delta-SG) knockout (KO) mice develop skeletal muscle histopathological alterations similar to those in humans with limb muscular dystrophy....
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SubjectTerms Animals
Ca 2+ transients
Calcium - physiology
Electric Stimulation
Hindlimb
Humans
Intracellular calcium
Mice
Mice, Inbred Strains
Mice, Knockout
Muscle fibers
Muscle Fibers, Skeletal - physiology
Muscle, Skeletal - metabolism
Muscular dystrophy
Muscular Dystrophy, Animal - genetics
Reference Values
Sarcoglycans - deficiency
Sarcoglycan–sarcospan complex
Sarcoplasmic reticulum
Signal Transduction - physiology
Title Intracellular Ca2+ transients in delta-sarcoglycan knockout mouse skeletal muscle
URI https://dx.doi.org/10.1016/j.bbagen.2009.11.011
https://www.ncbi.nlm.nih.gov/pubmed/19931597
https://www.proquest.com/docview/733786185
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