Fibroblast growth factor 7 stimulates in vitro growth of oocytes originating from bovine early antral follicles

Essential factors required for growing oocytes derived from bovine early antral follicles and their mechanisms of action are poorly understood. Fibroblast growth factor 7 (FGF7) is a member of the heparin‐binding FGF family with a distinctive pattern of target‐cell specificity. The effect of FGF7 on...

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Veröffentlicht in:Molecular reproduction and development 2008-12, Vol.75 (12), p.1736-1743
Hauptverfasser: Cho, Joon-Ho, Itoh, Takehiro, Sendai, Yutaka, Hoshi, Hiroyoshi
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container_issue 12
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container_title Molecular reproduction and development
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creator Cho, Joon-Ho
Itoh, Takehiro
Sendai, Yutaka
Hoshi, Hiroyoshi
description Essential factors required for growing oocytes derived from bovine early antral follicles and their mechanisms of action are poorly understood. Fibroblast growth factor 7 (FGF7) is a member of the heparin‐binding FGF family with a distinctive pattern of target‐cell specificity. The effect of FGF7 on the stimulation of oocyte growth in a culture of cumulus–oocyte complexes with granulosa cells (COCGs, oocyte diameter; 90–100 µm) was investigated. The oocyte diameter of COCGs was increased significantly in the FGF7‐containing medium (10 ng/ml; 117.2 ± 3.2 µm, 50 ng/ml; 116.5 ± 3.5 µm) compared to the control (0 ng/ml; 110.5 ± 2.8 µm) after 16 days. However, there was no stimulatory effect of FGF7 on the proliferation of cumulus‐granulosa cells. The FGF7 receptor, fibroblast growth factor receptor 2IIIb (FGFR2IIIb), was detected in cumulus‐granulosa cells from COCGs. Messenger RNA expression of FGFR2IIIb was induced to cumulus‐granulosa cells by FGF7. The mRNA expression levels of KIT ligand (KITLG), KIT (KIT), growth differentiation factor 9 (GDF9), and bone morphogenetic protein 15 (BMP15) in the cultured COCGs were determined in FGF7‐treated (10 ng/ml) cultures using real time RT‐PCR analysis. The levels of KITLG and KIT, but not GDF9 and BMP15 mRNA expression were stimulated by FGF7. Furthermore, neutralizing antibody for KIT attenuated the stimulatory action of FGF7 on the oocyte growth. These results strongly suggest that FGF7 may be an important regulator for oocyte growth and its action is mediated via the KIT/KITLG signaling pathway. Mol. Reprod. Dev. 75: 1736–1743, 2008. © 2008 Wiley‐Liss, Inc.
doi_str_mv 10.1002/mrd.20912
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Fibroblast growth factor 7 (FGF7) is a member of the heparin‐binding FGF family with a distinctive pattern of target‐cell specificity. The effect of FGF7 on the stimulation of oocyte growth in a culture of cumulus–oocyte complexes with granulosa cells (COCGs, oocyte diameter; 90–100 µm) was investigated. The oocyte diameter of COCGs was increased significantly in the FGF7‐containing medium (10 ng/ml; 117.2 ± 3.2 µm, 50 ng/ml; 116.5 ± 3.5 µm) compared to the control (0 ng/ml; 110.5 ± 2.8 µm) after 16 days. However, there was no stimulatory effect of FGF7 on the proliferation of cumulus‐granulosa cells. The FGF7 receptor, fibroblast growth factor receptor 2IIIb (FGFR2IIIb), was detected in cumulus‐granulosa cells from COCGs. Messenger RNA expression of FGFR2IIIb was induced to cumulus‐granulosa cells by FGF7. The mRNA expression levels of KIT ligand (KITLG), KIT (KIT), growth differentiation factor 9 (GDF9), and bone morphogenetic protein 15 (BMP15) in the cultured COCGs were determined in FGF7‐treated (10 ng/ml) cultures using real time RT‐PCR analysis. The levels of KITLG and KIT, but not GDF9 and BMP15 mRNA expression were stimulated by FGF7. Furthermore, neutralizing antibody for KIT attenuated the stimulatory action of FGF7 on the oocyte growth. These results strongly suggest that FGF7 may be an important regulator for oocyte growth and its action is mediated via the KIT/KITLG signaling pathway. Mol. Reprod. 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Reprod. Dev</addtitle><description>Essential factors required for growing oocytes derived from bovine early antral follicles and their mechanisms of action are poorly understood. Fibroblast growth factor 7 (FGF7) is a member of the heparin‐binding FGF family with a distinctive pattern of target‐cell specificity. The effect of FGF7 on the stimulation of oocyte growth in a culture of cumulus–oocyte complexes with granulosa cells (COCGs, oocyte diameter; 90–100 µm) was investigated. The oocyte diameter of COCGs was increased significantly in the FGF7‐containing medium (10 ng/ml; 117.2 ± 3.2 µm, 50 ng/ml; 116.5 ± 3.5 µm) compared to the control (0 ng/ml; 110.5 ± 2.8 µm) after 16 days. However, there was no stimulatory effect of FGF7 on the proliferation of cumulus‐granulosa cells. The FGF7 receptor, fibroblast growth factor receptor 2IIIb (FGFR2IIIb), was detected in cumulus‐granulosa cells from COCGs. Messenger RNA expression of FGFR2IIIb was induced to cumulus‐granulosa cells by FGF7. 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Psychology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Gene Expression Regulation - physiology</topic><topic>Growth Differentiation Factor 9 - biosynthesis</topic><topic>Hormone metabolism and regulation</topic><topic>KIT ligand</topic><topic>Mammalian female genital system</topic><topic>oocyte growth</topic><topic>Oocytes - cytology</topic><topic>Oocytes - metabolism</topic><topic>Proto-Oncogene Proteins c-kit - biosynthesis</topic><topic>Receptor, Fibroblast Growth Factor, Type 2 - biosynthesis</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - physiology</topic><topic>Stem Cell Factor - biosynthesis</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Joon-Ho</creatorcontrib><creatorcontrib>Itoh, Takehiro</creatorcontrib><creatorcontrib>Sendai, Yutaka</creatorcontrib><creatorcontrib>Hoshi, Hiroyoshi</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Joon-Ho</au><au>Itoh, Takehiro</au><au>Sendai, Yutaka</au><au>Hoshi, Hiroyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fibroblast growth factor 7 stimulates in vitro growth of oocytes originating from bovine early antral follicles</atitle><jtitle>Molecular reproduction and development</jtitle><addtitle>Mol. Reprod. Dev</addtitle><date>2008-12</date><risdate>2008</risdate><volume>75</volume><issue>12</issue><spage>1736</spage><epage>1743</epage><pages>1736-1743</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><coden>MREDEE</coden><abstract>Essential factors required for growing oocytes derived from bovine early antral follicles and their mechanisms of action are poorly understood. Fibroblast growth factor 7 (FGF7) is a member of the heparin‐binding FGF family with a distinctive pattern of target‐cell specificity. The effect of FGF7 on the stimulation of oocyte growth in a culture of cumulus–oocyte complexes with granulosa cells (COCGs, oocyte diameter; 90–100 µm) was investigated. The oocyte diameter of COCGs was increased significantly in the FGF7‐containing medium (10 ng/ml; 117.2 ± 3.2 µm, 50 ng/ml; 116.5 ± 3.5 µm) compared to the control (0 ng/ml; 110.5 ± 2.8 µm) after 16 days. However, there was no stimulatory effect of FGF7 on the proliferation of cumulus‐granulosa cells. The FGF7 receptor, fibroblast growth factor receptor 2IIIb (FGFR2IIIb), was detected in cumulus‐granulosa cells from COCGs. Messenger RNA expression of FGFR2IIIb was induced to cumulus‐granulosa cells by FGF7. The mRNA expression levels of KIT ligand (KITLG), KIT (KIT), growth differentiation factor 9 (GDF9), and bone morphogenetic protein 15 (BMP15) in the cultured COCGs were determined in FGF7‐treated (10 ng/ml) cultures using real time RT‐PCR analysis. The levels of KITLG and KIT, but not GDF9 and BMP15 mRNA expression were stimulated by FGF7. Furthermore, neutralizing antibody for KIT attenuated the stimulatory action of FGF7 on the oocyte growth. These results strongly suggest that FGF7 may be an important regulator for oocyte growth and its action is mediated via the KIT/KITLG signaling pathway. Mol. Reprod. Dev. 75: 1736–1743, 2008. © 2008 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18386286</pmid><doi>10.1002/mrd.20912</doi><tpages>8</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Bone Morphogenetic Protein 15 - biosynthesis
Cattle
Cell Enlargement - drug effects
Cells, Cultured
Coculture Techniques
Cumulus Cells - cytology
Cumulus Cells - metabolism
Female
FGF7
Fibroblast Growth Factor 7 - metabolism
Fibroblast Growth Factor 7 - pharmacology
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation - drug effects
Gene Expression Regulation - physiology
Growth Differentiation Factor 9 - biosynthesis
Hormone metabolism and regulation
KIT ligand
Mammalian female genital system
oocyte growth
Oocytes - cytology
Oocytes - metabolism
Proto-Oncogene Proteins c-kit - biosynthesis
Receptor, Fibroblast Growth Factor, Type 2 - biosynthesis
RNA, Messenger - biosynthesis
Signal Transduction - drug effects
Signal Transduction - physiology
Stem Cell Factor - biosynthesis
Vertebrates: reproduction
title Fibroblast growth factor 7 stimulates in vitro growth of oocytes originating from bovine early antral follicles
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