Literature DB >> 26962112

Behavior of Mouse Spermatozoa in the Female Reproductive Tract from Soon after Mating to the Beginning of Fertilization.

Yuko Muro1, Hidetoshi Hasuwa1, Ayako Isotani1, Haruhiko Miyata1, Kazuo Yamagata1, Masahito Ikawa1, Ryuzo Yanagimachi2, Masaru Okabe3.   

Abstract

Using transgenic mice with spermatozoa expressing enhanced green fluorescent protein in their acrosome and red fluorescent protein in their midpiece mitochondria, we followed the behavior of spermatozoa within the female genital tract after natural mating. When examined 15 min after coitus, many spermatozoa were around the opening of the uterotubal junction. Spermatozoa that entered the uterotubal junction were seemingly not moving, yet they steadily migrated toward the isthmus at a speed only time-lapse video recording could demonstrate. Many spermatozoa reaching the lower isthmus were motile. The site where spermatozoa attached and detached from the isthmus epithelium shifted from the lower to the upper segment of the isthmus with time. Virtually all the live spermatozoa within the lower isthmus were acrosome intact, whereas many of the actively motile spermatozoa in the upper isthmus were acrosome reacted. As far as we could observe, all the spermatozoa we found within the lumen of the ampulla and the cumulus oophorus were acrosome reacted. Even though we saw only a very few spermatozoa within the ampulla during fertilization, all were associated with, or were already within, oocytes, indicating that mouse fertilization in vivo is extremely efficient.
© 2016 by the Society for the Study of Reproduction, Inc.

Entities:  

Keywords:  ampulla; isthmus; mouse; oviduct; sperm migration; uterotubal junction

Mesh:

Year:  2016        PMID: 26962112     DOI: 10.1095/biolreprod.115.135368

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  38 in total

1.  Monitoring dimeric status of IZUMO1 during the acrosome reaction in living spermatozoon.

Authors:  Naokazu Inoue; Ikuo Wada
Journal:  Cell Cycle       Date:  2018-07-25       Impact factor: 4.534

2.  Detection of extracellular vesicles in the mouse vaginal fluid: Their delivery of sperm proteins that stimulate capacitation and modulate fertility.

Authors:  Zeinab Fereshteh; Pradeepthi Bathala; Deni S Galileo; Patricia A Martin-DeLeon
Journal:  J Cell Physiol       Date:  2018-12-07       Impact factor: 6.384

Review 3.  Sperm success and immunity.

Authors:  Stuart Wigby; Susan S Suarez; Brian P Lazzaro; Tommaso Pizzari; Mariana F Wolfner
Journal:  Curr Top Dev Biol       Date:  2019-05-15       Impact factor: 4.897

4.  In vivo three-dimensional tracking of sperm behaviors in the mouse oviduct.

Authors:  Shang Wang; Irina V Larina
Journal:  Development       Date:  2018-03-19       Impact factor: 6.868

5.  Disruption of protein kinase A localization induces acrosomal exocytosis in capacitated mouse sperm.

Authors:  Cintia Stival; Carla Ritagliati; Xinran Xu; Maria G Gervasi; Guillermina M Luque; Carolina Baró Graf; José Luis De la Vega-Beltrán; Nicolas Torres; Alberto Darszon; Diego Krapf; Mariano G Buffone; Pablo E Visconti; Dario Krapf
Journal:  J Biol Chem       Date:  2018-04-26       Impact factor: 5.157

Review 6.  Post-ejaculatory modifications to sperm (PEMS).

Authors:  Scott Pitnick; Mariana F Wolfner; Steve Dorus
Journal:  Biol Rev Camb Philos Soc       Date:  2019-11-18

7.  An intact acrosome is required for the chemotactic response to progesterone in mouse spermatozoa.

Authors:  Hector A Guidobaldi; Noritaka Hirohashi; Marisa Cubilla; Mariano G Buffone; Laura C Giojalas
Journal:  Mol Reprod Dev       Date:  2017-02-28       Impact factor: 2.609

Review 8.  Roles of steroid hormones in oviductal function

Authors:  Brooke Barton; Gerardo Herrera; Prashanth Anamthathmakula; Jenna Rock; Anna Willie; Emily Harris; Ken-Ichi Takemaru; Wipawee Winuthayanon
Journal:  Reproduction       Date:  2020-03-01       Impact factor: 3.906

9.  Creatine enhances the duration of sperm capacitation: a novel factor for improving in vitro fertilization with small numbers of sperm.

Authors:  Takashi Umehara; Tomoko Kawai; Masaaki Goto; JoAnne S Richards; Masayuki Shimada
Journal:  Hum Reprod       Date:  2018-06-01       Impact factor: 6.918

10.  PGAP6, a GPI-specific phospholipase A2, has narrow substrate specificity against GPI-anchored proteins.

Authors:  Gun-Hee Lee; Morihisa Fujita; Hideki Nakanishi; Haruhiko Miyata; Masahito Ikawa; Yusuke Maeda; Yoshiko Murakami; Taroh Kinoshita
Journal:  J Biol Chem       Date:  2020-08-18       Impact factor: 5.157

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