Literature DB >> 30827999

Development of a Ligand Screening Tool Using Full-Length Human Peroxisome Proliferator-Activated Receptor-Expressing Cell Lines to Ameliorate Metabolic Syndrome.

Keisuke Tachibana1, Kenji Ishimoto1, Rika Takahashi1, Hirokazu Kadono1, Takuya Awaji1, Tomohiro Yuzuriha2, Toshiya Tanaka3, Takao Hamakubo4, Juro Sakai5, Tatsuhiko Kodama3, Shunji Aoki6, Takefumi Doi1.   

Abstract

Peroxisome proliferator-activated receptors (PPARs) belong to the nuclear hormone receptor superfamily and include three subtypes (PPARα, PPARδ, and PPARγ). They regulate gene expression in a ligand-dependent manner. PPARα plays an important role in lipid metabolism. PPARγ is involved in glucose metabolism and is a potential therapeutic target in Type 2 diabetes. PPARδ ligands are candidates for the treatment of metabolic disorders. Thus, the detection of PPAR ligands may facilitate the treatment of various diseases. In this study, to identify PPAR ligands, we engineered reporter cell lines that can be used to quantify PPARγ and PPARδ activity. We evaluated several known ligands using these reporter cell lines and confirmed that they are useful for PPAR ligand detection. Furthermore, we evaluated extracts of approximately 200 natural resources and found various extracts that enhance reporter gene activity. Finally, we identified a main alkaloid of the Evodia fruit, evodiamine, as a PPARγ activator using this screening tool. These results suggest that the established reporter cell lines may serve as a useful cell-based screening tool for finding PPAR ligands to ameliorate metabolic syndromes.

Entities:  

Keywords:  Tet-off system; ligand; natural resource; nuclear receptor; peroxisome proliferator-activated receptor; screening system

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Year:  2019        PMID: 30827999     DOI: 10.1248/cpb.c18-00627

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  2 in total

1.  On the Inhibitability of Natural Products Isolated from Tetradium ruticarpum towards Tyrosine Phosphatase 1B (PTP1B) and α-Glucosidase (3W37): An In Vitro and In Silico Study.

Authors:  Dao-Cuong To; Thanh Q Bui; Nguyen Thi Ai Nhung; Quoc-Toan Tran; Thi-Thuy Do; Manh-Hung Tran; Phan-Phuoc Hien; Truong-Nhan Ngu; Phan-Tu Quy; The-Hung Nguyen; Huu-Tho Nguyen; Tien-Dung Nguyen; Phi-Hung Nguyen
Journal:  Molecules       Date:  2021-06-17       Impact factor: 4.411

Review 2.  Chemical Screening of Nuclear Receptor Modulators.

Authors:  Mari Ishigami-Yuasa; Hiroyuki Kagechika
Journal:  Int J Mol Sci       Date:  2020-07-31       Impact factor: 5.923

  2 in total

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