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Published on: March 1, 2019
Alpha6beta1 integrin expressed by sperm is determinant in mouse fertilization
Virginie Barraud-Lange1, Nathalie Naud-Barriant, Line Saffar
1Biologie de la Reproduction, UFR SMBH, Université Paris 13, Bobigny, France, Service d'Histologie-Embryologie-Cytogénétique, Hôpital Jean Verdier (AP-HP), Bondy, France. raud@smbh.univ-paris13.fr
BMC Developmental Biology
|September 14, 2007
Summary
Alpha6beta1 integrin is present on both sperm and egg cells, playing a role in fertilization. Its presence on either gamete can be sufficient for successful mouse fertilization.
Area of Science:
- Reproductive biology
- Cellular and molecular biology
- Integrin signaling
Background:
- Previous studies suggested alpha6beta1 integrin as a sperm receptor based on inhibition tests.
- Gene deletion experiments indicated that oocyte alpha6 or beta1 integrin subunits are not essential for mouse fertilization.
Purpose of the Study:
- To investigate the expression and function of alpha6beta1 integrin in mouse gametes.
- To clarify the role of alpha6beta1 integrin in sperm-egg interaction and fertilization.
Main Methods:
- Western blot analysis and immunofluorescence to detect alpha6beta1 integrin expression in sperm.
- Inhibition assays using anti-alpha6 antibody (GoH3) to assess functional impact on sperm.
- Fusion tests with zona-intact and zona-free eggs to evaluate the role of the zona pellucida and oocyte integrin.
Main Results:
- Alpha6beta1 integrin was confirmed to be expressed on mouse sperm.
- Inhibition of sperm alpha6beta1 integrin by anti-alpha6 antibody specifically impaired sperm fertilizing ability.
- Bypassing the zona pellucida in fusion tests indicated that oocyte alpha6beta1 integrin's function is not essential when sperm integrin is functional.
Conclusions:
- Alpha6beta1 integrin is expressed on both sperm and oocytes and is functional in gamete membrane interactions.
- The presence of alpha6beta1 integrin on either gamete can compensate for its absence on the other, enabling fertilization.
- Membrane fragment exchange between gametes prior to fusion may contribute to this rescue mechanism.
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