Title of article
Expression of c-Jun in human granulosa cells from patients participating in in vitro fertilization programs
Author/Authors
Hassani Bafrani، Hassan نويسنده Gametogenesis Research Center, Kashan University of Medical Sciences, Kashan, Iran , , Saito، Hidekazu نويسنده ,
Issue Information
فصلنامه با شماره پیاپی سال 2008
Pages
5
From page
175
To page
179
Abstract
Background: The mitogen-activated protein kinase (MAPK) pathway is one of the
major signaling pathways that transmit intracellular signals initiated by extracellular
stimuli to the nucleus. The stress-activated protein kinase (SAPK)/c-Jun NH2-terminal
kinase is a subfamily of MAP kinases implicated in cytokine and stress responses.
Objective: In this study, we have examined total and phosphorylated c-Jun in the mural
and cumulus granulosa cells, and investigated also whether c-Jun can be responsible for
the difference in the expression of apoptosis between mural and cumulus regions.
Materials and Methods: A total of 14 consecutive couples participating in IVF
program were investigated. Aspirated follicular fluid was transferred into tissue culture
dishes and oocyte-cumulus cells complexes were isolated. The cells were centrifuge and
fixed with Bouin’s solution and then were put on a glass slide. After fixation, the slides
were stained by immunocytochemistry method.
The incidence of apoptotic granulosa cells was examined by a fluorescence microscope.
Results: The incidence of apoptotic granulosa cells was 1.27 ± 0.12 in the mural region
and 0.38 ± 0.07 in the cumulus regions.
All mural and cumulus cells expressed total c-Jun in 7 patients while phosphorylated c-
Jun was also expressed in all cells of the other 7 patients. There was no difference
between apoptotic and nonapoptotic cells in the expression of total and phosphorylated
c-Jun.
Conclusion: C-Jun may not be responsible for apoptotic effect on mural and cumulus
cells.
Journal title
International Journal of Reproductive BioMedicine
Serial Year
2008
Journal title
International Journal of Reproductive BioMedicine
Record number
2391646
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