作者: Tongxing Song , Jie Peng , Jiao Ren , Hong-kui Wei , Jian Peng
DOI: 10.1155/2015/813816
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摘要: The polyunsaturated fatty acids (PUFAs) receptor GPR120 exerts a significant impact on systemic nutrient homeostasis in human and rodents. However, the porcine (pGPR120) has not been well characterized. In current study, we found that pGPR120 had 3 spliced variants. Transcript 1 encoded 362-amino (aa) wild type pGPR120-WT, which shared 88% homology with short form GPR120. was mainly expressed transcript of pGPR120. It predominantly ileum, jejunum, duodenum, spleen, adipose. (coding 320-aa isoform) detected while 2 310-aa only slightly spleen. A selective agonist for (TUG-891) PUFAs activated SRE-luc NFAT-luc reporter HEK293T cells transfected construct pGPR120-WT but pGPR120-V2. isoform dominant negative isoform. extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation levels were by PUFAs, especially n-3 PUFA. These results showed although transcripts, transcript. TUG-891 PUFA, pGPR120-WT. study contributed to dissecting molecular regulation mechanisms PUFA pigs.