Molecular Cloning and Recombinant Expression of the Long Form of Leptin Receptor (Ob-Rb) cDNA as Isolated from Rat Spleen

  • Ju, Sung-Kyu (Protein Engineering Laboratory, Korea Research Institute of Bioscience and Biotechnology) ;
  • Park, Jung-Hyun (Protein Engineering Laboratory, Korea Research Institute of Bioscience and Biotechnology) ;
  • Na, Shin-Young (Protein Engineering Laboratory, Korea Research Institute of Bioscience and Biotechnology) ;
  • You, Kwan-Hee (Department of Biology, College of Natural Sciences, Chungnam National University) ;
  • Kim, Kil-Lyong (Protein Engineering Laboratory, Korea Research Institute of Bioscience and Biotechnology) ;
  • Lee, Myung-Kyu (Protein Engineering Laboratory, Korea Research Institute of Bioscience and Biotechnology)
  • Received : 2000.10.31
  • Accepted : 2001.01.19
  • Published : 2001.03.31

Abstract

Leptin is a circulating non-glycosylated protein that is mainly produced in adipocytes. Leptin acts in the brain to regulate food intake and energy expenditure. Previously we reported our success in the isolation of a partial cDNA of the long form of the leptin receptor, OB-Rb, from rat spleen, and showed that leptin might also play a role in peripheral immune organs. In the present study, for the first time, the complete coding region of OB-Rb cDNA was cloned from rat splenocytes, and its nucleotide sequence was determined. The cDNA was then further expressed in E. coli and mammalian cells, thereby confirming the functional integrity of this receptor. Prokaryotically overexpressed OB-R protein was then used as an immunizing antigen in BALE/c mice to produce leptin receptor-specific antibodies. By using them, we confirmed the cell surface expression of OB-Rb in transfected CHO cells. It is our belief that the reagents, as produced in this study, will be of great use in further studies of the biological role of rat leptin.

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