Retinoid acid-induced microRNA-27b-3p impairs C2C12 myoblast proliferation and differentiation by suppressing α-dystrobrevin

2017 ◽  
Vol 350 (2) ◽  
pp. 301-311 ◽  
Author(s):  
Nan Li ◽  
Yi Tang ◽  
Bo Liu ◽  
Wei Cong ◽  
Chao Liu ◽  
...  
2018 ◽  
Vol 97 (4) ◽  
pp. 257-268 ◽  
Author(s):  
Han Wang ◽  
Qian Zhang ◽  
BinBin Wang ◽  
WangJun Wu ◽  
Julong Wei ◽  
...  

Author(s):  
Tomoya Kitakaze ◽  
Meiku Oshimo ◽  
Yasuyuki Kobayashi ◽  
Mizuyuki Ryu ◽  
Yasushi Suzuki ◽  
...  

Marine Drugs ◽  
2021 ◽  
Vol 19 (5) ◽  
pp. 266
Author(s):  
Seo-Young Kim ◽  
Ji-Hyeok Lee ◽  
Nalae Kang ◽  
Kil-Nam Kim ◽  
You-Jin Jeon

Skeletal muscle is an important tissue in energy metabolism and athletic performance. The use of effective synthetic supplements and drugs to promote muscle growth is limited by various side effects. Moreover, their use is prohibited by anti-doping agencies; hence, natural alternatives are needed. Therefore, we evaluated the muscle growth effect of substances that can act like synthetic supplements from edible marine algae. First, we isolated six marine algal polyphenols belonging to the phlorotannin class, namely dieckol (DK), 2,7′′-phloroglucinol-6,6′-bieckol (PHB), phlorofucofuroeckol A (PFFA), 6,6′-bieckol (6,6-BK), pyrogallol-phloroglucinol-6,6′-bieckol (PPB), and phloroglucinol (PG) from an edible brown alga, Ecklonia cava and evaluated their effects on C2C12 myoblasts proliferation and differentiation. Of the six phlorotannin isolates evaluated, DK and PHB induced the highest degree of C2C12 myoblast proliferation. In addition, DK and PHB regulates myogenesis by down-regulating the Smad signaling, a negative regulator, and up-regulating the insulin-like growth factor-1 (IGF-1) signaling, a positive regulator. Interestingly, DK and PHB bind strongly to myostatin, which is an inhibitor of myoblast proliferation, while also binding to IGF-1 receptors. Moreover, they bind to IGF-1 receptor. These results suggest that DK and PHB are potential natural muscle building supplements and could be a safer alternative to synthetic drugs.


2016 ◽  
Vol 6 ◽  
pp. 39-46 ◽  
Author(s):  
Luce Pèrié ◽  
Alexis Parenté ◽  
Caroline Brun ◽  
Laetitia Magnol ◽  
Patrick Pélissier ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Piyaporn Surinlert ◽  
Nitchamon Kongthong ◽  
Mariam Watthanard ◽  
Thannicha Sae-lao ◽  
Piyawat Sookbangnop ◽  
...  

Contaminations of chemicals in foods and drinks are raising public concerns. Among these, styrene, a monomer for plastic production, receives increasing interest due to its ability to leach from the packaging and contaminate in foods and drinks causing many health problems. The present study was designed to investigate the effects of styrene monomer (STR) and its metabolite styrene oxide (STO) on C2C12 myoblast proliferation and differentiation. Based on an MTT assay, both STR and STO showed no cytotoxic effect at 10–100 μM. However, at 50–100 μM STO, but not STR, significantly inhibited cell proliferation. The STO-treated cells were accumulated in S-phase of cell cycles as revealed by flow cytometry. The antioxidant enzyme (catalase and superoxide dismutase) activities and the gene expressing these enzymes of the arrested cells were decreased and ultimately led to nuclear condensation and expression of apoptotic markers such as cleaved caspase-3 and-9, but not cleaved caspase-8. In addition, STO significantly suppressed myogenic differentiation by decreasing both the number and size of differentiated myotubes. Biochemical analysis showed attenuations of total protein synthesis and myosin heavy chain (MHC) protein expression. In conclusion, a metabolite of styrene, STO, leached from plastic packaging of foods and beverages suppressed both myoblast proliferation and differentiation, which would affect skeletal muscle development and regeneration.


Author(s):  
Shion Osana ◽  
Yasuo Kitajima ◽  
Naoki Suzuki ◽  
Aki Nunomiya ◽  
Hiroaki Takada ◽  
...  

2013 ◽  
Vol 27 (S1) ◽  
Author(s):  
Piming Zhao ◽  
Li Xu ◽  
Andrew T. Mariano ◽  
Renzhi Han

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