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FSH modulatory effect on human granulosa cells: a gene-protein candidate for gonadotrophin surge-attenuating factor

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Autor
Karligiotou, E.; Kollia, P.; Papaggeli, P.; Samara, S.; Vagena, A.; Dafopoulos, K.; Messinis, I. E.
Datum
2011
DOI
10.1016/j.rbmo.2011.06.005
Schlagwort
FSH
GnSAF
human granulosa cells
human serum albumin
FOLLICLE-STIMULATING-HORMONE
HUMAN MENOPAUSAL GONADOTROPIN
LUTEINIZING-HORMONE
FACTOR GNSAF
INHIBITING FACTOR
OVARIAN
HYPERSTIMULATION
SUPEROVULATION INDUCTION
NUCLEOTIDE-SEQUENCE
OVULATION INDUCTION
PITUITARY-RESPONSE
Obstetrics & Gynecology
Reproductive Biology
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Zusammenfassung
Previous evidence indicates a homology of gonadotrophin surge-attenuating factor (GnSAF) to the carboxyl terminal of human serum albumin (HSA) and the ability of human granulosa cells to produce mRNA transcripts corresponding to this fragment, but the underlying mechanism is still unknown. This study investigated the role of FSH in vitro in the expression of the carboxyl terminal of HSA by human luteinized granulosa cells. Cells were cultured on poly-L-lysine-coated microscope slides in the absence or presence of 10 ng/ml FSH, followed by in-situ hybridization and immunocytochemistry. In the presence of FSH, mRNA transcripts corresponding to the carboxyl terminal of the HSA gene and corresponding protein could be detected in comparable intensity to that seen by hepatic HepG2 cells (positive control). Significantly lower expression was detected in granulosa cells cultured without FSH addition (P < 0.01), but no expression was detected in HeLa cells. These results demonstrate for the first time that FSH stimulates the expression of the carboxyl terminal fragment of the HSA gene and corresponding protein in human luteinized granulosa cells. Therefore, the carboxyl terminal of HSA has a functional role in the ovary and this further supports the notion that this HSA fragment is a GnSAF-bioactive entity. (C) 2011, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
URI
http://hdl.handle.net/11615/29158
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