The regulation of adipogenesis through GPR120

التفاصيل البيبلوغرافية
العنوان: The regulation of adipogenesis through GPR120
المؤلفون: Chizu Gotoh, Daisuke Hishikawa, Tetsuya Adachi, Sang Houn Song, Yeon Hee Hong, Ki-choon Choi, Yasuki Suzuki, Akira Hirasawa, Shinichi Sasaki, Tomoyo Iga, Sang Gun Roh, Gozoh Tsujimoto
المصدر: Biochemical and Biophysical Research Communications. 354:591-597
بيانات النشر: Elsevier BV, 2007.
سنة النشر: 2007
مصطلحات موضوعية: medicine.medical_specialty, Adipose tissue macrophages, Biophysics, Adipose tissue, White adipose tissue, Biochemistry, Receptors, G-Protein-Coupled, Mice, chemistry.chemical_compound, 3T3-L1 Cells, Internal medicine, Adipocyte, Adipocytes, medicine, Animals, adipocyte protein 2, Molecular Biology, Messenger RNA, Adipogenesis, biology, Chemistry, 3T3-L1, Cell Biology, Mice, Inbred C57BL, Endocrinology, biology.protein, Female
الوصف: Recently, it has been found that long-chain fatty acids activate the G protein-coupled receptors (GPRs), GPR120 and GPR40. However, there have been no reports to date on the possible physiological roles of these GPRs in adipose tissue development and adipocyte differentiation. GPR120 mRNA was highly expressed in the four different adipose tissues, and the amount of mRNA was elevated in adipose tissues of mice fed a high fat diet. However, GPR40 mRNA was not detected in any of the adipose tissues. The expression of GPR120 mRNA was higher in adipocytes compared to stromal-vascular (S-V) cells. The level of GPR120 mRNA increased during adipocyte differentiation in 3T3-L1 cells. Similar results were observed in human adipose tissue, human preadipocytes, and cultured adipocytes. Moreover, use of a small interference RNA (siRNA) to down-regulate GPR120 expression resulted in inhibition of adipocyte differentiation. Our results suggest that GPR120 regulates adipogenic processes such as adipocyte development and differentiation.
تدمد: 0006-291X
DOI: 10.1016/j.bbrc.2007.01.028
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86d0d5b1b7506fef4a36b2f8fdfa0964
https://doi.org/10.1016/j.bbrc.2007.01.028
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....86d0d5b1b7506fef4a36b2f8fdfa0964
قاعدة البيانات: OpenAIRE
الوصف
تدمد:0006291X
DOI:10.1016/j.bbrc.2007.01.028