1α,25(OH)2D3-glycosides fromSolanum glaucophyllumleaves extract induce myoblasts differentiation through p38 MAPK and AKT activation
Author(s) -
A.P. Irazoqui,
Pablo De Genaro,
Claudia Buitrago,
Heinrich Bachmann,
Verónica González Pardo,
Ana Russo de Boland
Publication year - 2018
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.033670
Subject(s) - biology , p38 mitogen activated protein kinases , protein kinase b , mapk/erk pathway , glycoside , solanum , botany , traditional medicine , microbiology and biotechnology , signal transduction , medicine
We have previously shown that Solanum glaucophyllum leaf extract (SGE) increases VDR protein levels and promotes myoblast differentiation. Here, we investigated whether p38 MAPK and AKT are involved in SGE actions. Cell-cycle studies showed that SGE prompted a peak of S-phase followed by an arrest in the G0/G1-phase through p38 MAPK. Time course studies showed that p38 MAPK and AKT phosphorylation were statistically increased by SGE (10 nM) or synthetic 1α,25(OH) 2 D 3 (1 nM) treatment. Furthermore, p38 MAPK and AKT inhibitors, SB203580 and LY294002 respectively, suppressed myoblasts fusion induced by SGE or synthetic 1α,25(OH) 2 D 3 We have also studied differentiation genes by qRT-PCR. myoD1 mRNA increased significantly by SGE (24-72 h) or 1α,25(OH) 2 D 3 (24 h) treatment. mRNA expression of myogenin also increased upon SGE or 1α,25(OH) 2 D 3 treatment. Finally, MHC2b mRNA expression, a late differentiation marker, was increased significantly by both compounds at 72 h compared to control. Taken together, these results suggest that SGE, as synthetic 1α,25(OH) 2 D 3 , promotes myotube formation through p38 MAPK and AKT activation.
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