RyR1 Is Involved in the Control of Myogenesis

被引:0
|
作者
Tourel, Amandine [1 ]
Reynaud-Dulaurier, Robin [1 ]
Brocard, Julie [1 ]
Faure, Julien [1 ]
Marty, Isabelle [1 ]
Petiot, Anne [1 ]
机构
[1] Univ Grenoble Alpes, Grenoble Inst Neurosci, Inserm, U1216,CHU Grenoble Alpes, F-38000 Grenoble, France
关键词
calcium; myogenesis; RyR1; MYOBLAST DIFFERENTIATION; ENDOPLASMIC-RETICULUM; RYANODINE RECEPTOR; MAMMALIAN TARGET; SKELETAL-MUSCLE; AMPK; ACTIVATION; METABOLISM; EXPRESSION; GLUCOSE;
D O I
10.3390/cells14030158
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The RyR1 calcium release channel is a key player in skeletal muscle excitation-contraction coupling. Mutations in the RYR1 gene are associated with congenital myopathies. Recently, a role of RyR1 in myotubes differentiation has been proposed and attributed to its calcium channel function, which nonetheless remains to be clearly demonstrated. In order to clarify RyR1 role in myogenesis, we have developed an in vitro model, the so-called RyR1-Rec myotubes, which are mouse primary myotubes with an inducible decrease in RyR1 protein amount and in RyR1-mediated calcium release. Using this model, we showed that the RyR1 protein decrease was responsible for an increase in both differentiation and fusion, from the RNA level to the morphological level, without affecting the myogenic factors MyoD and MyoG. Although an increase in mTOR pathway was observed in RyR1-Rec myotubes, it did not seem to be responsible for the role of RyR1 in myogenesis. Additionally, even if modulation of intracellular calcium level affected RyR1-Rec myotubes differentiation, we have shown that the role of RyR1 in myogenesis was independent of its calcium channel function. Therefore, our findings indicate that, besides its pivotal role as a calcium channel responsible for muscle contraction, RyR1 fulfills a calcium-independent inhibitor function of myogenesis.
引用
收藏
页数:19
相关论文
共 50 条
  • [21] FRET-based mapping of calmodulin bound to the RyR1 Ca2+ release channel
    Cornea, Razvan L.
    Nitu, Florentin
    Gruber, Simon
    Kohler, Katherine
    Satzer, Michael
    Thomas, David D.
    Fruen, Bradley R.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (15) : 6128 - 6133
  • [22] Common variants in RYR1 are associated with left ventricular hypertrophy assessed by electrocardiogram
    Hong, Kyung-Won
    Shin, Dong-Jik
    Lee, Sang-Hak
    Son, Nak-Hoon
    Go, Min-Jin
    Lim, Ji-Eun
    Shin, Chol
    Jang, Yangsoo
    Oh, Bermseok
    EUROPEAN HEART JOURNAL, 2012, 33 (10) : 1250 - 1256
  • [23] The RyR1 P3528S Substitution Alters Mouse Skeletal Muscle Contractile Properties and RyR1 Ion Channel Gating
    Thekkedam, Chris G.
    Dutka, Travis L.
    van der Poel, Chris
    Burgio, Gaetan
    Dulhunty, Angela F.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (01)
  • [24] Unveiling the intricate role of S100A1 in regulating RyR1 activity: A commentary on "Structural insights into the regulation of RyR1 by S100A1"
    Perry, Megan L.
    Varney, Kristen M.
    Tiwary, Pratyush
    Weber, David J.
    Hernandez-Ochoa, Erick O.
    CELL CALCIUM, 2024, 123
  • [25] Moderate intensity continuous training reverses the detrimental effects of ovariectomy on RyR1 phosphorylation in rat skeletal muscle
    Zuegel, M.
    Wehrstein, F.
    Qiu, S.
    Diel, P.
    Steinacker, M.
    Schumann, U.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2019, 481 : 1 - 7
  • [26] Allosteric modulation of ryanodine receptor RyR1 by nucleotide derivatives
    Cholak, Spencer
    Saville, James W.
    Zhu, Xing
    Berezuk, Alison M.
    Tuttle, Katharine S.
    Haji-Ghassemi, Omid
    Alvarado, Francisco J.
    Van Petegem, Filip
    Subramaniam, Sriram
    STRUCTURE, 2023, 31 (07) : 790 - +
  • [27] Malignant hyperthermia in infancy and identification of novel RYR1 mutation
    Chamley, D
    Pollock, NA
    Stowell, KM
    Brown, RL
    BRITISH JOURNAL OF ANAESTHESIA, 2000, 84 (04) : 500 - 504
  • [28] The elusive role of the SPRY2 domain in RyR1
    Tae, HanShen
    Wei, Lan
    Willemse, Hermia
    Mirza, Shamaruh
    Gallant, Esther M.
    Board, Philip G.
    Dirksen, Robert T.
    Casarotto, Marco G.
    Dulhunty, Angela F.
    CHANNELS, 2011, 5 (02) : 148 - 160
  • [29] Mutations in RYR1 in malignant hyperthermia and central core disease
    Robinson, Rachel
    Carpenter, Danielle
    Shaw, Marie-Anne
    Halsall, Jane
    Hopkins, Philip
    HUMAN MUTATION, 2006, 27 (10) : 977 - 989
  • [30] A novel missense mutation of RYR1 in familial idiopathic hyper CK-emia
    Sano, Ken
    Miura, Shiroh
    Fujiwara, Toshiya
    Fujioka, Ryuta
    Yorita, Akiko
    Noda, Kazuhito
    Kida, Hiroshi
    Azuma, Koichi
    Kaieda, Shinjiro
    Yamamoto, Ken
    Taniwaki, Takayuki
    Fukumaki, Yasuyuki
    Shibata, Hiroki
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2015, 356 (1-2) : 142 - 147