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Citric acid cycle intermediates as ligands for orphan G-protein-coupled receptors

Author

Listed:
  • Weihai He

    (Tularik Inc.
    Genospectra Inc.)

  • Frederick J.-P. Miao

    (Tularik Inc.)

  • Daniel C.-H. Lin

    (Tularik Inc.)

  • Ralf T. Schwandner

    (Tularik Inc.
    Tularik GmbH)

  • Zhulun Wang

    (Tularik Inc.)

  • Jinhai Gao

    (Tularik Inc.
    Novartis Institute of Biomedical Research Inc.)

  • Jin-Long Chen

    (Tularik Inc.)

  • Hui Tian

    (Tularik Inc.)

  • Lei Ling

    (Tularik Inc.)

Abstract

The citric acid cycle is central to the regulation of energy homeostasis and cell metabolism1. Mutations in enzymes that catalyse steps in the citric acid cycle result in human diseases with various clinical presentations2. The intermediates of the citric acid cycle are present at micromolar concentration in blood and are regulated by respiration, metabolism and renal reabsorption/extrusion. Here we show that GPR91 (ref. 3), a previously orphan G-protein-coupled receptor (GPCR), functions as a receptor for the citric acid cycle intermediate succinate. We also report that GPR99 (ref. 4), a close relative of GPR91, responds to α-ketoglutarate, another intermediate in the citric acid cycle. Thus by acting as ligands for GPCRs, succinate and α-ketoglutarate are found to have unexpected signalling functions beyond their traditional roles. Furthermore, we show that succinate increases blood pressure in animals. The succinate-induced hypertensive effect involves the renin–angiotensin system and is abolished in GPR91-deficient mice. Our results indicate a possible role for GPR91 in renovascular hypertension, a disease closely linked to atherosclerosis, diabetes and renal failure5,6.

Suggested Citation

  • Weihai He & Frederick J.-P. Miao & Daniel C.-H. Lin & Ralf T. Schwandner & Zhulun Wang & Jinhai Gao & Jin-Long Chen & Hui Tian & Lei Ling, 2004. "Citric acid cycle intermediates as ligands for orphan G-protein-coupled receptors," Nature, Nature, vol. 429(6988), pages 188-193, May.
  • Handle: RePEc:nat:nature:v:429:y:2004:i:6988:d:10.1038_nature02488
    DOI: 10.1038/nature02488
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    1. Adam M. Zahm & William S. Owens & Samuel R. Himes & Braden S. Fallon & Kathleen E. Rondem & Alexa N. Gormick & Joshua S. Bloom & Sriram Kosuri & Henry Chan & Justin G. English, 2024. "A massively parallel reporter assay library to screen short synthetic promoters in mammalian cells," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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