Cargando…

Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization

BACKGROUND: Studies have examined the function of PI 3-kinase in the early developmental processes that operate in oocytes or early embryos of various species. However, the roles of egg-associated PI 3-kinase and Akt, especially in signal transduction at fertilization, are not well understood. RESUL...

Descripción completa

Detalles Bibliográficos
Autores principales: Mammadova, Gunay, Iwasaki, Tetsushi, Tokmakov, Alexander A, Fukami, Yasuo, Sato, Ken-ichi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805626/
https://www.ncbi.nlm.nih.gov/pubmed/20015408
http://dx.doi.org/10.1186/1471-213X-9-68
_version_ 1782176205791821824
author Mammadova, Gunay
Iwasaki, Tetsushi
Tokmakov, Alexander A
Fukami, Yasuo
Sato, Ken-ichi
author_facet Mammadova, Gunay
Iwasaki, Tetsushi
Tokmakov, Alexander A
Fukami, Yasuo
Sato, Ken-ichi
author_sort Mammadova, Gunay
collection PubMed
description BACKGROUND: Studies have examined the function of PI 3-kinase in the early developmental processes that operate in oocytes or early embryos of various species. However, the roles of egg-associated PI 3-kinase and Akt, especially in signal transduction at fertilization, are not well understood. RESULTS: Here we show that in Xenopus eggs, a potent inhibitor of phosphatidylinositol 3-kinase (PI 3-kinase), LY294002 inhibits sperm-induced activation of the tyrosine kinase Src and a transient increase in the intracellular concentration of Ca(2+ )at fertilization. LY294002 also inhibits sperm-induced dephosphorylation of mitogen-activated protein kinase, breakdown of cyclin B2 and Mos, and first embryonic cleavage, all of which are events of Ca(2+)-dependent egg activation. In fertilized eggs, an 85-kDa subunit of PI 3-kinase (p85) undergoes a transient translocation to the low-density, detergent-insoluble membranes (membrane microdomains) where Src tyrosine kinase signaling is operating. However, the tyrosine phosphorylation of p85 in fertilized eggs is not as evident as that in H2O2-activated eggs, arguing against the possibility that PI 3-kinase is activated by Src phosphorylation. Nevertheless, sperm-induced activation of PI 3-kinase has been demonstrated by the finding that Akt, a serine/threonine-specific protein kinase, is phosphorylated at threonine-308. The threonine-phosphorylated Akt also localizes to the membrane microdomains of fertilized eggs. Application of bp(V), an inhibitor of PTEN that dephosphorylates PIP3, the enzymatic product of PI 3-kinase, promotes parthenogenetic activation of Xenopus eggs. In vitro kinase assays demonstrate that PIP3 activates Src in a dose-dependent manner. CONCLUSIONS: These results suggest that PI 3-kinase is involved in sperm-induced egg activation via production of PIP3 that would act as a positive regulator of the Src signaling pathway in Xenopus fertilization.
format Text
id pubmed-2805626
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-28056262010-01-13 Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization Mammadova, Gunay Iwasaki, Tetsushi Tokmakov, Alexander A Fukami, Yasuo Sato, Ken-ichi BMC Dev Biol Research article BACKGROUND: Studies have examined the function of PI 3-kinase in the early developmental processes that operate in oocytes or early embryos of various species. However, the roles of egg-associated PI 3-kinase and Akt, especially in signal transduction at fertilization, are not well understood. RESULTS: Here we show that in Xenopus eggs, a potent inhibitor of phosphatidylinositol 3-kinase (PI 3-kinase), LY294002 inhibits sperm-induced activation of the tyrosine kinase Src and a transient increase in the intracellular concentration of Ca(2+ )at fertilization. LY294002 also inhibits sperm-induced dephosphorylation of mitogen-activated protein kinase, breakdown of cyclin B2 and Mos, and first embryonic cleavage, all of which are events of Ca(2+)-dependent egg activation. In fertilized eggs, an 85-kDa subunit of PI 3-kinase (p85) undergoes a transient translocation to the low-density, detergent-insoluble membranes (membrane microdomains) where Src tyrosine kinase signaling is operating. However, the tyrosine phosphorylation of p85 in fertilized eggs is not as evident as that in H2O2-activated eggs, arguing against the possibility that PI 3-kinase is activated by Src phosphorylation. Nevertheless, sperm-induced activation of PI 3-kinase has been demonstrated by the finding that Akt, a serine/threonine-specific protein kinase, is phosphorylated at threonine-308. The threonine-phosphorylated Akt also localizes to the membrane microdomains of fertilized eggs. Application of bp(V), an inhibitor of PTEN that dephosphorylates PIP3, the enzymatic product of PI 3-kinase, promotes parthenogenetic activation of Xenopus eggs. In vitro kinase assays demonstrate that PIP3 activates Src in a dose-dependent manner. CONCLUSIONS: These results suggest that PI 3-kinase is involved in sperm-induced egg activation via production of PIP3 that would act as a positive regulator of the Src signaling pathway in Xenopus fertilization. BioMed Central 2009-12-17 /pmc/articles/PMC2805626/ /pubmed/20015408 http://dx.doi.org/10.1186/1471-213X-9-68 Text en Copyright ©2009 Mammadova et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Mammadova, Gunay
Iwasaki, Tetsushi
Tokmakov, Alexander A
Fukami, Yasuo
Sato, Ken-ichi
Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
title Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
title_full Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
title_fullStr Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
title_full_unstemmed Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
title_short Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
title_sort evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in xenopus egg fertilization
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805626/
https://www.ncbi.nlm.nih.gov/pubmed/20015408
http://dx.doi.org/10.1186/1471-213X-9-68
work_keys_str_mv AT mammadovagunay evidencethatphosphatidylinositol3kinaseisinvolvedinsperminducedtyrosinekinasesignalinginxenopuseggfertilization
AT iwasakitetsushi evidencethatphosphatidylinositol3kinaseisinvolvedinsperminducedtyrosinekinasesignalinginxenopuseggfertilization
AT tokmakovalexandera evidencethatphosphatidylinositol3kinaseisinvolvedinsperminducedtyrosinekinasesignalinginxenopuseggfertilization
AT fukamiyasuo evidencethatphosphatidylinositol3kinaseisinvolvedinsperminducedtyrosinekinasesignalinginxenopuseggfertilization
AT satokenichi evidencethatphosphatidylinositol3kinaseisinvolvedinsperminducedtyrosinekinasesignalinginxenopuseggfertilization