Impaired febrile response in mice lacking the prostaglandin E receptor subtype EP3 (original) (raw)
- Letter
- Published: 17 September 1998
- Eri Segi2 na1,
- Yukihiko Sugimoto2,
- Takahiko Murata1,
- Toshiyuki Matsuoka1,
- Takuya Kobayashi1,
- Hiroko Hizaki2,
- Kazuhito Tuboi2,
- Masato Katsuyama2,
- Atsushi Ichikawa2,
- Takashi Tanaka3,
- Nobuaki Yoshida3 &
- …
- Shuh Narumiya1
Nature volume 395, pages 281–284 (1998)Cite this article
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Abstract
Fever, a hallmark of disease, is elicited by exogenous pyrogens, that is, cellular components, such as lipopolysaccharide (LPS), of infectious organisms, as well as by non-infectious inflammatory insults. Both stimulate the production of cytokines, such as interleukin (IL)-1β, that act on the brain as endogenous pyrogens1. Fever can be suppressed by aspirin-like anti-inflammatory drugs. As these drugs share the ability to inhibit prostaglandin biosynthesis2, it is thought that a prostaglandin is important in fever generation. Prostaglandin E2 (PGE2) may be a neural mediator of fever3, but this has been much debated1,4,5,6,7. PGE2 acts by interacting with four subtypes of PGE receptor, the EP1, EP2, EP3 and EP4 receptors8. Here we generate mice lacking each of these receptors by homologous recombination. Only mice lacking the EP3 receptor fail to show a febrile response to PGE2 and to either IL-1β or LPS. Our results establish that PGE2 mediates fever generation in response to both exogenous and endogenous pyrogens by acting at the EP3 receptor.
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Acknowledgements
We thank Y. Kataoka and K. Ishikawa for injection of embryonic stem cells, K.Takahashi for animal breeding, and K. Okuyama and T. Arai for secretarial assistance. This work was supported by grants-in-aid from the Ministry of Education, Science, Sports and Culture of Japan and from the Ministry of Health and Welfare of Japan, and by grants from the Uehara Memorial Foundation, the Smoking Research Foundation and the Japanese Foundation on Metabolism and Diseases.
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Author notes
- Fumitaka Ushikubi and Eri Segi: These authors contributed equally to this work.
Authors and Affiliations
- Department of Pharmacology, and Department of Physiological Chemistry, Faculty of Medicine, Faculty of Pharmaceutical Sciences, Kyoto University, 606-8315, Kyoto, Japan
Fumitaka Ushikubi, Takahiko Murata, Toshiyuki Matsuoka, Takuya Kobayashi & Shuh Narumiya - Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, 606-8315, Kyoto, Japan
Eri Segi, Yukihiko Sugimoto, Hiroko Hizaki, Kazuhito Tuboi, Masato Katsuyama & Atsushi Ichikawa - Division of Molecular and Cellular Immunology, Research Institute, Osaka Medical Center for Maternal and Child Health, 594-1101, Osaka, Japan
Takashi Tanaka & Nobuaki Yoshida
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- Fumitaka Ushikubi
You can also search for this author inPubMed Google Scholar - Eri Segi
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You can also search for this author inPubMed Google Scholar - Toshiyuki Matsuoka
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You can also search for this author inPubMed Google Scholar - Kazuhito Tuboi
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You can also search for this author inPubMed Google Scholar - Atsushi Ichikawa
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Correspondence toShuh Narumiya.
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Ushikubi, F., Segi, E., Sugimoto, Y. et al. Impaired febrile response in mice lacking the prostaglandin E receptor subtype EP3.Nature 395, 281–284 (1998). https://doi.org/10.1038/26233
- Received: 07 April 1998
- Accepted: 09 July 1998
- Issue Date: 17 September 1998
- DOI: https://doi.org/10.1038/26233
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