TY - JOUR
T1 - Self-Exposure to the Male Pheromone ESP1 Enhances Male Aggressiveness in Mice
AU - Hattori, Tatsuya
AU - Osakada, Takuya
AU - Matsumoto, Ayaka
AU - Matsuo, Naoki
AU - Haga-Yamanaka, Sachiko
AU - Nishida, Takaya
AU - Mori, Yuji
AU - Mogi, Kazutaka
AU - Touhara, Kazushige
AU - Kikusui, Takefumi
N1 - Funding Information:
This study was supported in part by Grants-in-Aid for Scientific Research on Innovative Areas (grants 4501 and 25132712 to T.K.; 25660252 to K.M.) from the Japan Society for the Promotion of Science (JSPS) , a Grant-in-Aid for Young Scientists (S) from JSPS (grant 19677002 ) to K.T., and a grant from the ERATO Touhara Chemosensory Signal Project from the Japan Science and Technology Agency to K.T. We thank K. Matsumura for assistance with mice generation. This paper is dedicated to Dr. Yuji Mori, who passed away during the preparation of the manuscript.
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/5/9
Y1 - 2016/5/9
N2 - Exocrine gland-secreting peptide 1 (ESP1) released into male tear fluids is a male pheromone that stimulates sexually receptive behavior in female mice via the vomeronasal sensory system. ESP1 also induces c-Fos expression in male brain regions distinct from those in females. However, behavior in males following ESP1 exposure has not been examined. In the present study, we show that ESP1, in conjunction with unfamiliar male urine, enhances male aggression via the specific vomeronasal receptor V2Rp5. In addition, male mice that secrete ESP1 but lack V2Rp5 exhibit a lower level of aggressiveness than do mice that express V2Rp5. These results suggest that ESP1 not only acts as a male pheromone in both sexes but also serves as an auto-stimulatory factor that enhances male aggressiveness by self-exposure. Finally, re-activation of ESP1-induced c-Fos-positive neurons by using the designer receptor exclusively activated by designer drug (DREADD) approach resulted in enhancement of sexual and aggressive behaviors in female and male mice, respectively, indicating that sexually dimorphic activation in the brain is a neural basis for the sex-specific behavioral responses to ESP1.
AB - Exocrine gland-secreting peptide 1 (ESP1) released into male tear fluids is a male pheromone that stimulates sexually receptive behavior in female mice via the vomeronasal sensory system. ESP1 also induces c-Fos expression in male brain regions distinct from those in females. However, behavior in males following ESP1 exposure has not been examined. In the present study, we show that ESP1, in conjunction with unfamiliar male urine, enhances male aggression via the specific vomeronasal receptor V2Rp5. In addition, male mice that secrete ESP1 but lack V2Rp5 exhibit a lower level of aggressiveness than do mice that express V2Rp5. These results suggest that ESP1 not only acts as a male pheromone in both sexes but also serves as an auto-stimulatory factor that enhances male aggressiveness by self-exposure. Finally, re-activation of ESP1-induced c-Fos-positive neurons by using the designer receptor exclusively activated by designer drug (DREADD) approach resulted in enhancement of sexual and aggressive behaviors in female and male mice, respectively, indicating that sexually dimorphic activation in the brain is a neural basis for the sex-specific behavioral responses to ESP1.
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U2 - 10.1016/j.cub.2016.03.029
DO - 10.1016/j.cub.2016.03.029
M3 - Article
C2 - 27151664
AN - SCOPUS:84963570014
SN - 0960-9822
VL - 26
SP - 1229
EP - 1234
JO - Current Biology
JF - Current Biology
IS - 9
ER -