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 in | Biochimica et biophysica acta Vol. 1800; no. 3; pp. 373 - 379 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.03.2010
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ISSN | 0304-4165 0006-3002 1872-8006 |
DOI | 10.1016/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. |
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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. |
Author_xml | – sequence: 1 givenname: Alhondra surname: Solares-Pérez fullname: Solares-Pérez, Alhondra organization: Unidad de Investigación Médica en Genética Humana, Hospital de Pediatría, CMN Siglo XXI-IMSS, México, D.F., Mexico – sequence: 2 givenname: Jorge A. surname: Sánchez fullname: Sánchez, Jorge A. organization: Departamento de Farmacología, Cinvestav-IPN, Av. IPN 2508, México, D.F., Mexico – sequence: 3 givenname: Alejandro surname: Zentella-Dehesa fullname: Zentella-Dehesa, Alejandro organization: Departamento de Bioquímica INNSZ and Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, UNAM, Mexico, D.F., Mexico – sequence: 4 givenname: María C. surname: García fullname: García, María C. email: cgarcia@cinvestav.mx organization: Departamento de Farmacología, Cinvestav-IPN, Av. IPN 2508, México, D.F., Mexico – sequence: 5 givenname: Ramón M. surname: Coral-Vázquez fullname: Coral-Vázquez, Ramón M. email: rmcoralv@prodigy.net.mx organization: Unidad de Investigación Médica en Genética Humana, Hospital de Pediatría, CMN Siglo XXI-IMSS, México, D.F., Mexico |
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CitedBy_id | crossref_primary_10_1016_j_ceca_2010_06_003 crossref_primary_10_1002_path_2799 crossref_primary_10_1186_2044_5040_4_13 crossref_primary_10_1371_journal_pone_0220904 crossref_primary_10_1098_rsos_200625 crossref_primary_10_1186_s13395_017_0127_9 |
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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 |
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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 |
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