Neurotensin Enhances Sperm Capacitation and Acrosome Reaction in Mice

• Published in: Biology of reproduction Vol. 91; no. 2; p. 53
• Main Authors: Hiradate, Yuuki, Inoue, Hiroki, Kobayashi, Norio, Shirakata, Yoshiki, Suzuki, Yutaka, Gotoh, Aina, Roh, Sang-gun, Uchida, Takafumi, Katoh, Kazuo, Yoshida, Manabu, Sato, Eimei, Tanemura, Kentaro
• Format: Journal Article
• Language: English
• Published: United States Society for the Study of Reproduction, Inc 01.08.2014
• Subjects: acrosome reaction; Acrosome Reaction - physiology; Animals; Calcium - metabolism; capacitation; cumulus cells; Dose-Response Relationship, Drug; Fallopian Tubes - metabolism; Female; fertilization; Gene Expression Regulation - physiology; Male; Mice; Neurotensin - metabolism; Neurotensin - pharmacology; oviduct; ovulation; Receptors, Neurotensin - genetics; Receptors, Neurotensin - metabolism; reproduction; RNA, Messenger - genetics; RNA, Messenger - metabolism; sperm; Sperm Capacitation - drug effects; Sperm Capacitation - physiology; Spermatozoa - physiology; uterus; Uterus - metabolism; oviduct; uterus; fertilization; capacitation; sperm; acrosome reaction; cumulus cells; ovulation; reproduction
• ISSN: 0006-3363; 1529-7268
• DOI: 10.1095/biolreprod.113.112789

Neurotensin (NT) has multiple functions, ranging from acting as a neurotransmitter to regulating intestinal movement. However, its function in reproductive physiology is unknown. Here, we confirmed the expression and localization of NT receptors (NTR1) in mouse epididymal spermatozoa and investigated the effect of NT on sperm function. Sperm protein tyrosine phosphorylation, one of the indices of sperm capacitation, was facilitated dose-dependently by NT administration. In addition, the acrosome reaction was promoted in capacitated spermatozoa, and addition of a selective antagonist of NTR1 and NTR2 blocked the induction. Furthermore, intracellular calcium mobilization by NT addition was observed. This showed that NT was an accelerator of sperm function via its functional receptors. The presence of NT was confirmed by immunohistochemistry and its localization was observed in epithelia of the uterus and oviduct isthmus and ampulla, which correspond to the fertilization route of spermatozoa. The NT mRNA level in ovulated cumulus cell was remarkably increased by treatment with human chorionic gonadotropin (hCG). Using an in vitro maturation model, we analyzed the effects of FSH, epidermal growth factor (EGF), estradiol, and progesterone in NT production in cumulus cells. We found that FSH and EGF upregulated NT release and mRNA expression. Both FSH- and EGF-induced upregulation were inhibited by U0126, an MAPK kinase inhibitor, indicating that FSH and EGF regulate NT expression via a MAPK-dependent pathway. This evidence suggests that NT can act as a promoter of sperm capacitation and the acrosome reaction in the female reproductive tract.