Author
Listed:
- Ko Kobayakawa
(Graduate School of Science, The University of Tokyo)
- Reiko Kobayakawa
(Graduate School of Science, The University of Tokyo)
- Hideyuki Matsumoto
(Graduate School of Medicine, The University of Tokyo)
- Yuichiro Oka
(Graduate School of Science, The University of Tokyo)
- Takeshi Imai
(Graduate School of Science, The University of Tokyo)
- Masahito Ikawa
(Research Institute for Microbial Diseases, The Osaka University)
- Masaru Okabe
(Research Institute for Microbial Diseases, The Osaka University)
- Toshio Ikeda
(Laboratory for Behavioral Genetics, Brain Science Institute, RIKEN, Saitama 351-0198, Japan)
- Shigeyoshi Itohara
(Laboratory for Behavioral Genetics, Brain Science Institute, RIKEN, Saitama 351-0198, Japan)
- Takefumi Kikusui
(Laboratory of Veterinary Ethology, The University of Tokyo)
- Kensaku Mori
(Graduate School of Medicine, The University of Tokyo)
- Hitoshi Sakano
(Graduate School of Science, The University of Tokyo)
Abstract
The mammalian olfactory system mediates various responses, including aversive behaviours to spoiled foods and fear responses to predator odours. In the olfactory bulb, each glomerulus represents a single species of odorant receptor. Because a single odorant can interact with several different receptor species, the odour information received in the olfactory epithelium is converted to a topographical map of multiple glomeruli activated in distinct areas in the olfactory bulb. To study how the odour map is interpreted in the brain, we generated mutant mice in which olfactory sensory neurons in a specific area of the olfactory epithelium are ablated by targeted expression of the diphtheria toxin gene. Here we show that, in dorsal-zone-depleted mice, the dorsal domain of the olfactory bulb was devoid of glomerular structures, although second-order neurons were present in the vacant areas. The mutant mice lacked innate responses to aversive odorants, even though they were capable of detecting them and could be conditioned for aversion with the remaining glomeruli. These results indicate that, in mice, aversive information is received in the olfactory bulb by separate sets of glomeruli, those dedicated for innate and those for learned responses.
Suggested Citation
Ko Kobayakawa & Reiko Kobayakawa & Hideyuki Matsumoto & Yuichiro Oka & Takeshi Imai & Masahito Ikawa & Masaru Okabe & Toshio Ikeda & Shigeyoshi Itohara & Takefumi Kikusui & Kensaku Mori & Hitoshi Saka, 2007.
"Innate versus learned odour processing in the mouse olfactory bulb,"
Nature, Nature, vol. 450(7169), pages 503-508, November.
Handle:
RePEc:nat:nature:v:450:y:2007:i:7169:d:10.1038_nature06281
DOI: 10.1038/nature06281
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Cited by:
- Chikako Nakajima & Masato Sawada & Erika Umeda & Yuma Takagi & Norihiko Nakashima & Kazuya Kuboyama & Naoko Kaneko & Satoaki Yamamoto & Haruno Nakamura & Naoki Shimada & Koichiro Nakamura & Kumiko Mat, 2024.
"Identification of the growth cone as a probe and driver of neuronal migration in the injured brain,"
Nature Communications, Nature, vol. 15(1), pages 1-19, December.
- Kevin W. Zhu & Shawn D. Burton & Maira H. Nagai & Justin D. Silverman & Claire A. March & Matt Wachowiak & Hiroaki Matsunami, 2022.
"Decoding the olfactory map through targeted transcriptomics links murine olfactory receptors to glomeruli,"
Nature Communications, Nature, vol. 13(1), pages 1-18, December.
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