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Chemotactic behavior of egg mitochondria in response to sperm fusion in mice

Mitochondria are the powerhouses of eukaryotic cells and their positioning contributes to fertilization and early developmental processes. We report that sperm fusion triggers Ca(2+) oscillations and mitochondrial movement toward fused sperm (mitochondrial chemotaxis) in mouse eggs. Mitochondria fun...

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Detalles Bibliográficos
Autores principales: Iwai, Maki, Harada, Yuichirou, Miyabayashi, Rinako, Kang, Woojin, Nakamura, Akihiro, Kawano, Natsuko, Miyamoto, Yoshitaka, Yamada, Mitsutoshi, Hamatani, Toshio, Miyado, Mami, Yoshida, Keiichi, Saito, Hidekazu, Tanaka, Mamoru, Umezawa, Akihiro, Miyado, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240845/
https://www.ncbi.nlm.nih.gov/pubmed/30480160
http://dx.doi.org/10.1016/j.heliyon.2018.e00944
Descripción
Sumario:Mitochondria are the powerhouses of eukaryotic cells and their positioning contributes to fertilization and early developmental processes. We report that sperm fusion triggers Ca(2+) oscillations and mitochondrial movement toward fused sperm (mitochondrial chemotaxis) in mouse eggs. Mitochondria functioned in Ca(2+) storage and were colocalized with endoplasmic reticulum (ER) during Ca(2+) oscillations. Mitochondria then moved toward the fused sperm. Sperm extracts lacking nuclei induced Ca(2+) oscillations, but did not promote mitochondrial chemotaxis. Our results suggest that sperm fusion motivates Ca(2+) oscillation-independent mitochondrial chemotaxis. This phenomenon indicates that egg mitochondria interact with sperm materials, presumably nuclear substances, and their network tethers egg and sperm nuclei at the early stage of zygote formation.