2015
DOI: 10.3109/10799893.2015.1056308
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GPR39 activates proliferation and differentiation of porcine intramuscular preadipocytes through targeting the PI3K/AKT cell signaling pathway

Abstract: It indicated that GPR39 was a transducer of Zn(2+), and enhanced proliferation and differentiation of porcine intramuscular preadipocytes through activation of the PI3K/Akt signaling pathway.

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Cited by 34 publications
(25 citation statements)
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“…The K2 cluster included genes that showed a notable overall trend of upregulation, suggesting their key roles over the entire process of differentiation. Members of this cluster, such as GPR39 and CHCHD4 , reportedly regulate the differentiation of porcine intramuscular preadipocytes (Dong et al 2016). However, their functions in chicken preadipocytes require experimental verification.…”
Section: Discussionmentioning
confidence: 99%
“…The K2 cluster included genes that showed a notable overall trend of upregulation, suggesting their key roles over the entire process of differentiation. Members of this cluster, such as GPR39 and CHCHD4 , reportedly regulate the differentiation of porcine intramuscular preadipocytes (Dong et al 2016). However, their functions in chicken preadipocytes require experimental verification.…”
Section: Discussionmentioning
confidence: 99%
“…Particular attention was paid to K2 cluster which included genes that underwent an overall trend of increase, suggesting their key roles over the entire differentiation process. Members from this cluster such as GPR39 and CHCHD4 had been reported to regulate the differentiation of preadipocytes(Dong et al, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, we found that the functions of genes migrated from RNA editing at A0 stage, to generation of precursor metabolites and energy at A2 stage and finally to regulation of cell death and apoptosis at A6 stage. As far as we know, quite a few pathways involved in preadipocytes differentiation have been validated to date, including the PI3K/AKT cell signaling pathway(Dong et al, 2016), LKB1-AMPK Pathway(Tung et al, 2016), Wnt/β-catenin signaling pathway(Lu et al, 2016; Mai et al, 2014; Zhang et al, 2014c), TGF-β pathway(Park et al, 2014), Bmp/Smad pathway(Liu et al, 2014; Suenaga et al, 2013), ERK signaling pathway(Chiang et al, 2013), PDK1/Akt pathway(He et al, 2013), p38 MAPK/ATF-2 and TOR/p70 S6 kinase pathways(Yan et al, 2013). However, little is known about pathways involved in preadipocytes differentiation of chicken.…”
Section: Discussionmentioning
confidence: 99%
“…VEPCs at a density of 1.0×10 4 /ml were collected from the cultures and replated into a 96-well plate and underwent different treatments. Cell proliferation was determined using MTT method according to the previous study (Dong et al 2016). A microplate reader was used to measure the absorbance at 450 nm (Bio-Rad, Hercules, CA, USA).…”
Section: Mtt Assaymentioning
confidence: 99%
“…Expression of Bcl-2 and VEGF in VEPCs was determined at indicated times by RNA preparation and quantitative reverse transcription polymerase chain reaction (RT-PCR). Total cellular RNA was isolated from cells on 6-well plates using Trizol reagent following the manufacturer's instructions (Invitrogen, Carlsbad, CA, USA) and RT-PCR was performed according to the reference (Dong et al 2016). β-actin expression was used as an internal control.…”
Section: Gene Expression Analysismentioning
confidence: 99%