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Mol. Cells 2001; 12(1): 131-136

Published online January 1, 1970

© The Korean Society for Molecular and Cellular Biology

Determination of Rat Leptin Activity In Vitro Using a Novel Luciferase Reporter Assay

Sung-Kyu Ju, Jung-Hyun Park, Shin-Young Na, Kwan-Hee You, KilLyong Kim, Myung-Kyu Lee

Abstract

Leptin is small cytokine-like protein that is involved in appetite and body weight regulation. Due to increased interest in using leptin as an anti-obesity reagent, re-combinant forms of leptin have been produced for several species, including humans, mice, rats, pigs, dogs, sheep etc. The biological activities of such re-combinant proteins were determined using various in vitro or in vivo systems; however so far, no specific as-say system for rat leptin is available. Since rats are representative animal models in obesity research, the establishment of a biological assay system for deter-mining rat leptin activity has been eagerly awaited. This study describes the generation of such a system using chinese hamster ovary (CHO)-cells that were transfected with the long form of the rat leptin recep-tor isoform, OB-Rb, whereby a signal transduces and activators of transcription-sensitive luciferase reporter system is further employed to quantify the leptin-mediated signals. This system is the first rat-specific leptin bioassay system that has been reported. It is expected that this assay will be used to further quan-tify and determine leptin activity from various biologi-cal fluids and sources.

Keywords Leptin, OB-Rb, Rat, Luciferase, Receptor.

Article

Communication

Mol. Cells 2001; 12(1): 131-136

Published online August 31, 2001

Copyright © The Korean Society for Molecular and Cellular Biology.

Determination of Rat Leptin Activity In Vitro Using a Novel Luciferase Reporter Assay

Sung-Kyu Ju, Jung-Hyun Park, Shin-Young Na, Kwan-Hee You, KilLyong Kim, Myung-Kyu Lee

Abstract

Leptin is small cytokine-like protein that is involved in appetite and body weight regulation. Due to increased interest in using leptin as an anti-obesity reagent, re-combinant forms of leptin have been produced for several species, including humans, mice, rats, pigs, dogs, sheep etc. The biological activities of such re-combinant proteins were determined using various in vitro or in vivo systems; however so far, no specific as-say system for rat leptin is available. Since rats are representative animal models in obesity research, the establishment of a biological assay system for deter-mining rat leptin activity has been eagerly awaited. This study describes the generation of such a system using chinese hamster ovary (CHO)-cells that were transfected with the long form of the rat leptin recep-tor isoform, OB-Rb, whereby a signal transduces and activators of transcription-sensitive luciferase reporter system is further employed to quantify the leptin-mediated signals. This system is the first rat-specific leptin bioassay system that has been reported. It is expected that this assay will be used to further quan-tify and determine leptin activity from various biologi-cal fluids and sources.

Keywords: Leptin, OB-Rb, Rat, Luciferase, Receptor.

Mol. Cells
Nov 30, 2023 Vol.46 No.11, pp. 655~725
COVER PICTURE
Kim et al. (pp. 710-724) demonstrated that a pathogen-derived Ralstonia pseudosolanacearum type III effector RipL delays flowering time and enhances susceptibility to bacterial infection in Arabidopsis thaliana. Shown is the RipL-expressing Arabidopsis plant, which displays general dampening of the transcriptional program during pathogen infection, grown in long-day conditions.

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