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PMID: 19605784 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Functional roles of mouse sperm hyaluronidases, HYAL5 and SPAM1, in fertilization.

Biology of reproduction ·Vol. 81 ·No. 5 ·2009-11-00 ·Pages 939-47

Kimura M, Kim E, Kang W, Yamashita M, Saigo M, Yamazaki T, Nakanishi T, Kashiwabara S, Baba T

Abstract

Although sperm entry into the oocyte-cumulus complex and subsequent sperm penetration through the cumulus matrix to reach the oocyte zona pellucida are essential for mammalian fertilization, the molecular mechanism remains controversial. Previously, we have shown that mouse sperm lacking SPAM1 are capable of penetrating the cumulus matrix despite a delayed dispersal of cumulus cells. We also have identified another sperm hyaluronidase, HYAL5, as a candidate enzyme involved in sperm penetration through the cumulus. In the present study, we produced HYAL5-deficient mice to uncover the functional roles of HYAL5 and SPAM1 in fertilization. The HYAL5-deficient mice were fully fertile and yielded normal litter sizes. In vitro fertilization assays demonstrated that HYAL5-deficient epididymal sperm is functionally normal. We thus conclude that HYAL5 may be dispensable for fertilization. Comparative analysis among wild-type, HYAL5-deficient, and SPAM1-deficient epididymal sperm revealed that only SPAM1 is probably involved in sperm penetration through the cumulus matrix. Notably, the loss of SPAM1 resulted in a remarkably increased accumulation of sperm on the surface or outer edge of the cumulus. These data suggest that SPAM1 may function in sperm entry into the cumulus and sperm penetration through the cumulus matrix.

MeSH Terms
Animals Blotting, Western Cell Adhesion Molecules/metabolism Cumulus Cells/metabolism Electrophoresis, Polyacrylamide Gel Enzyme Assays Epididymis/metabolism Female Fertilization/physiology Fertilization in Vitro Hyaluronoglucosaminidase/metabolism Litter Size Male Mice Mice, Knockout Oocytes/metabolism Sperm Capacitation Sperm-Ovum Interactions Spermatozoa/metabolism Time Factors Zona Pellucida/metabolism
Chemicals
Cell Adhesion Molecules Hyal5 protein, mouse Hyaluronoglucosaminidase hyaluronidase PH-20
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Kimura Masanori
Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba Science City, Ibaraki, Japan.
Kim Ekyune
Kang Woojin
Yamashita Misuzu
Saigo Mariko
Yamazaki Taiga
Nakanishi Tomoko
Kashiwabara Shin-ichi
Baba Tadashi
Article Info
Journal
Biology of reproduction
Abbr.
Biol Reprod
ISSN
1529-7268
Published
2009-11-00
Epub
2009-00-15
Pages
939-47
Language
English
Region
United States
NLM ID
0207224
Subset
IM
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