Dstac Regulates Excitation-Contraction Coupling inDrosophilaBody Wall Muscles

被引:2
作者
Hsu, I-Uen [1 ]
Linsley, Jeremy W. [1 ,2 ]
Reid, Lilly E. [1 ]
Hume, Richard I. [1 ]
Leflein, Ari [1 ]
Kuwada, John Y. [1 ,2 ]
机构
[1] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USA
关键词
stac adaptor protein; Drosophila; muscle; L-type voltage-gated calcium channel; excitation-contraction coupling; SKELETAL-MUSCLE; CALCIUM-CHANNEL; SARCOPLASMIC-RETICULUM; RYANODINE RECEPTOR; CHARGE MOVEMENT; CA2+ RELEASE; STAC3; SUBUNIT; GENE; EXPRESSION;
D O I
10.3389/fphys.2020.573723
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Stac3 regulates excitation-contraction coupling (EC coupling) in vertebrate skeletal muscles by regulating the L-type voltage-gated calcium channel (Ca(v)channel). Recently astac-like gene,Dstac, was identified inDrosophilaand found to be expressed by both a subset of neurons and muscles. Here, we show that Dstac and Dmca1D, theDrosophilaL-type Ca(v)channel, are necessary for normal locomotion by larvae. Immunolabeling with specific antibodies against Dstac and Dmca1D found that Dstac and Dmca1D are expressed by larval body-wall muscles. Furthermore, Ca(2+)imaging of muscles of Dstac and Dmca1D deficient larvae found that Dstac and Dmca1D are required for excitation-contraction coupling. Finally, Dstac appears to be required for normal expression levels of Dmca1D in body-wall muscles. These results suggest that Dstac regulates Dmca1D during EC coupling and thus muscle contraction.
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页数:11
相关论文
共 37 条
[1]   INTRAMEMBRANE CHARGE MOVEMENT RESTORED IN DYSGENIC SKELETAL-MUSCLE BY INJECTION OF DIHYDROPYRIDINE RECEPTOR CDNAS [J].
ADAMS, BA ;
TANABE, T ;
MIKAMI, A ;
NUMA, S ;
BEAM, KG .
NATURE, 1990, 346 (6284) :569-572
[2]   STRUCTURAL EVIDENCE FOR DIRECT INTERACTION BETWEEN THE MOLECULAR-COMPONENTS OF THE TRANSVERSE TUBULE SARCOPLASMIC-RETICULUM JUNCTION IN SKELETAL-MUSCLE [J].
BLOCK, BA ;
IMAGAWA, T ;
CAMPBELL, KP ;
FRANZINIARMSTRONG, C .
JOURNAL OF CELL BIOLOGY, 1988, 107 (06) :2587-2600
[3]   Excitation-contraction coupling in gastrointestinal and other smooth muscles [J].
Bolton, TB ;
Prestwich, SA ;
Zholos, AV ;
Gordienko, DV .
ANNUAL REVIEW OF PHYSIOLOGY, 1999, 61 :85-115
[4]   Excitation-contraction coupling in skeletal muscle fibers from adult domestic honeybee [J].
Collet, Claude .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2009, 458 (03) :601-612
[5]   The SH3 and cysteine-rich domain 3 (Stac3) gene is important to growth, fiber composition, and calcium release from the sarcoplasmic reticulum in postnatal skeletal muscle [J].
Cong, Xiaofei ;
Doering, Jonathan ;
Mazala, Davi A. G. ;
Chin, Eva R. ;
Grange, Robert W. ;
Jiang, Honglin .
SKELETAL MUSCLE, 2016, 6
[6]   The Ca2+ influx through the mammalian skeletal muscle dihydropyridine receptor is irrelevant for muscle performance [J].
Dayal, Anamika ;
Schroetter, Kai ;
Pan, Yuan ;
Foehr, Karl ;
Melzer, Werner ;
Grabner, Manfred .
NATURE COMMUNICATIONS, 2017, 8
[7]  
Eberl DF, 1998, GENETICS, V148, P1159
[8]   Genetic screen in Drosophila muscle identifies autophagy-mediated T-tubule remodeling and a Rab2 role in autophagy [J].
Fujita, Naonobu ;
Huang, Wilson ;
Lin, Tzu-han ;
Groulx, Jean-Francois ;
Jean, Steve ;
Jen Nguyen ;
Kuchitsu, Yoshihiko ;
Koyama-Honda, Ikuko ;
Mizushima, Noboru ;
Fukuda, Mitsunori ;
Kiger, Amy A. .
ELIFE, 2017, 6
[9]   Stac3 Inhibits Myoblast Differentiation into Myotubes [J].
Ge, Xiaomei ;
Zhang, Yafei ;
Park, Sungwon ;
Cong, Xiaofei ;
Gerrard, David E. ;
Jiang, Honglin .
PLOS ONE, 2014, 9 (04)
[10]   Microfluidic Chips for In Vivo Imaging of Cellular Responses to Neural Injury in Drosophila Larvae [J].
Ghannad-Rezaie, Mostafa ;
Wang, Xing ;
Mishra, Bibhudatta ;
Collins, Catherine ;
Chronis, Nikos .
PLOS ONE, 2012, 7 (01)