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2015 Fiscal Year Final Research Report

Cellular and molecular studies on expression of sperm functional proteins relating with infertility using gene-modified mouse lines

Research Project

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Project/Area Number 25293041
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section一般
Research Field General anatomy (including histology/embryology)
Research InstitutionChiba University

Principal Investigator

Toshimori Kiyotaka  千葉大学, 未来医療教育研究センター, 特任教授 (20094097)

Co-Investigator(Kenkyū-buntansha) Ito Chizuru  千葉大学, 大学院医学研究院, 講師 (80347054)
Co-Investigator(Renkei-kenkyūsha) Maekawa Mamiko  千葉大学, 大学院医学研究院, 助教 (20181571)
Kamimura Kyouko  千葉大学, 大学院医学研究院, 技術専門職員 (20422264)
Mutoh Tohru  千葉大学, 大学院医学研究院, 技術専門職員 (30422265)
Project Period (FY) 2013-04-01 – 2016-03-31
Keywords精子 / 遺伝子改変マウス / 受精 / 不妊 / エクアトリン / equatorin
Outline of Final Research Achievements

Using the established Eqtn-Tg(EGFP) and Eqtn-KO mouse lines, we analyzed live-images of the acrosome region that is the sperm fusion site for egg and molecular change from the acrosome reaction throughout to egg activation. A whole cell imaging (80-100nm acrosomal membrane complex) of sperm was obtained by new microscopy STED system without sectioning, which suggested a possibility of live cell imaging during fertilization (Microscopy, 2015). We clarified the distribution abnormality of gamete fusion-related spesp1 in the Eqtn-knockout (KO) mouse line, fertility loss of the Eqtn/Spesp1 double KO mouse line and relations with other gamete-fusion related proteins. Based on these analyses, we proposed the novel mechanism of sperm membrane modifications leading to gamete fusion in mammals including humans. Manuscripts showing these events are prepared for publication.

Free Research Field

精子

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Published: 2017-05-10  

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