Insulin-like growth factor-I stimulates the expression of 3 beta-hydroxysteroid dehydrogenase messenger ribonucleic acid in ovarian theca-interstitial cells
Evidence accumulating in the literature supports the hypothesis that insulin-like growth factor-I (IGF-I) may play a role in stimulating differentiation of the ovarian theca-interstitial cells (TIC) during early follicular development. IGF-I has been shown to synergistically enhance the stimulation...
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Veröffentlicht in: | Biology of reproduction 1993-05, Vol.48 (5), p.1166-1173 |
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creator | MAGOFFIN, D. A WEITSMAN, S. R |
description | Evidence accumulating in the literature supports the hypothesis that insulin-like growth factor-I (IGF-I) may play a role
in stimulating differentiation of the ovarian theca-interstitial cells (TIC) during early follicular development. IGF-I has
been shown to synergistically enhance the stimulation of androgen biosynthesis and to increase LH binding in TIC. The purpose
of the present studies was to examine the role of IGF-I in TIC differentiation by determining the effects of IGF-I on 3 beta-hydroxysteroid
dehydrogenase (3 beta-HSD) mRNA expression in TIC stimulated to differentiate in vitro. TIC were isolated from the ovaries
of hypophysectomized immature rats by Percoll gradient centrifugation and cultured in the presence and absence of LH and IGF-I
for up to 6 days. At various times cytoplasmic RNA was extracted from the TIC, and 3 beta-HSD mRNA was measured by specific
assay using reverse transcription followed by the polymerase chain reaction. Amplification of 3 beta-HSD mRNA using primers
designed to distinguish between the type I and type II 3 beta-HSD gene products revealed that the TIC expressed primarily
the type I gene. Increasing concentrations of LH (0-1 microgram/ml) stimulated a dose-related increase in 3 beta-HSD mRNA
that was approximately 3-fold at 100 ng/ml of LH. Addition of IGF-I (30 ng/ml) increased 3 beta-HSD mRNA approximately 2-fold
over TIC treated with LH alone. |
doi_str_mv | 10.1095/biolreprod48.5.1166 |
format | Article |
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in stimulating differentiation of the ovarian theca-interstitial cells (TIC) during early follicular development. IGF-I has
been shown to synergistically enhance the stimulation of androgen biosynthesis and to increase LH binding in TIC. The purpose
of the present studies was to examine the role of IGF-I in TIC differentiation by determining the effects of IGF-I on 3 beta-hydroxysteroid
dehydrogenase (3 beta-HSD) mRNA expression in TIC stimulated to differentiate in vitro. TIC were isolated from the ovaries
of hypophysectomized immature rats by Percoll gradient centrifugation and cultured in the presence and absence of LH and IGF-I
for up to 6 days. At various times cytoplasmic RNA was extracted from the TIC, and 3 beta-HSD mRNA was measured by specific
assay using reverse transcription followed by the polymerase chain reaction. Amplification of 3 beta-HSD mRNA using primers
designed to distinguish between the type I and type II 3 beta-HSD gene products revealed that the TIC expressed primarily
the type I gene. Increasing concentrations of LH (0-1 microgram/ml) stimulated a dose-related increase in 3 beta-HSD mRNA
that was approximately 3-fold at 100 ng/ml of LH. Addition of IGF-I (30 ng/ml) increased 3 beta-HSD mRNA approximately 2-fold
over TIC treated with LH alone.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod48.5.1166</identifier><identifier>PMID: 8386947</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>3-Hydroxysteroid Dehydrogenases - genetics ; Animals ; Base Sequence ; Biological and medical sciences ; Cell Differentiation ; DNA Restriction Enzymes ; Female ; Fundamental and applied biological sciences. Psychology ; Gene Expression - drug effects ; Hormone metabolism and regulation ; Insulin-Like Growth Factor I - pharmacology ; Kinetics ; Luteinizing Hormone - pharmacology ; Mammalian female genital system ; Molecular Sequence Data ; Polymerase Chain Reaction ; Progesterone - biosynthesis ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - metabolism ; Theca Cells - enzymology ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 1993-05, Vol.48 (5), p.1166-1173</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4745197$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8386947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MAGOFFIN, D. A</creatorcontrib><creatorcontrib>WEITSMAN, S. R</creatorcontrib><title>Insulin-like growth factor-I stimulates the expression of 3 beta-hydroxysteroid dehydrogenase messenger ribonucleic acid in ovarian theca-interstitial cells</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>Evidence accumulating in the literature supports the hypothesis that insulin-like growth factor-I (IGF-I) may play a role
in stimulating differentiation of the ovarian theca-interstitial cells (TIC) during early follicular development. IGF-I has
been shown to synergistically enhance the stimulation of androgen biosynthesis and to increase LH binding in TIC. The purpose
of the present studies was to examine the role of IGF-I in TIC differentiation by determining the effects of IGF-I on 3 beta-hydroxysteroid
dehydrogenase (3 beta-HSD) mRNA expression in TIC stimulated to differentiate in vitro. TIC were isolated from the ovaries
of hypophysectomized immature rats by Percoll gradient centrifugation and cultured in the presence and absence of LH and IGF-I
for up to 6 days. At various times cytoplasmic RNA was extracted from the TIC, and 3 beta-HSD mRNA was measured by specific
assay using reverse transcription followed by the polymerase chain reaction. Amplification of 3 beta-HSD mRNA using primers
designed to distinguish between the type I and type II 3 beta-HSD gene products revealed that the TIC expressed primarily
the type I gene. Increasing concentrations of LH (0-1 microgram/ml) stimulated a dose-related increase in 3 beta-HSD mRNA
that was approximately 3-fold at 100 ng/ml of LH. Addition of IGF-I (30 ng/ml) increased 3 beta-HSD mRNA approximately 2-fold
over TIC treated with LH alone.</description><subject>3-Hydroxysteroid Dehydrogenases - genetics</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Differentiation</subject><subject>DNA Restriction Enzymes</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression - drug effects</subject><subject>Hormone metabolism and regulation</subject><subject>Insulin-Like Growth Factor I - pharmacology</subject><subject>Kinetics</subject><subject>Luteinizing Hormone - pharmacology</subject><subject>Mammalian female genital system</subject><subject>Molecular Sequence Data</subject><subject>Polymerase Chain Reaction</subject><subject>Progesterone - biosynthesis</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - metabolism</subject><subject>Theca Cells - enzymology</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcuu1DAMQCMEugwXvgAhZYHYdUiaR9MluuIx0pXYwLrKw50G0nRIUnrnX_hYMjCCjS3ZR8eWjdBLSvaU9OKt8UtIcEqL42ov9pRK-QjtqGj7pmuleox2hBDZMCbZU_Qs52-EUM5adoNuFFOy590O_TrEvAYfm-C_Az6mZSsTHrUtS2oOOBc_r0EXyLhMgOHhlCBnv0S8jJhhA0U309ml5eGcC6TFO-zgT-EIUWfAc8UhHiHh5M0SVxvAW6xtBX2V_NTJ63hxW934WBV1YvE6YAsh5OfoyahDhhfXfIu-fnj_5e5Tc__54-Hu3X0ztVKWhivHW02ss72iLR97KhU3QjsmRtcJ2jkpyAjEcBBGyM6N2pjRqlYyZqCGW_Tmr7fe8scKuQyzz5cNdIRlzUMnOiIZVxV8dQVXM4MbTsnPOp2H6zlr__W1r7PVYUw6Wp__Ybzjgvbd_3mTP06bTzDkWYdQpWzYto2rQQyXb7LfzLuYmQ</recordid><startdate>19930501</startdate><enddate>19930501</enddate><creator>MAGOFFIN, D. A</creator><creator>WEITSMAN, S. R</creator><general>Society for the Study of Reproduction</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19930501</creationdate><title>Insulin-like growth factor-I stimulates the expression of 3 beta-hydroxysteroid dehydrogenase messenger ribonucleic acid in ovarian theca-interstitial cells</title><author>MAGOFFIN, D. A ; WEITSMAN, S. R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h266t-48d42a0cdc98124f91684b5ad35fd7517d650fe0b4e5b567dfabbfc82633be633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>3-Hydroxysteroid Dehydrogenases - genetics</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cell Differentiation</topic><topic>DNA Restriction Enzymes</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression - drug effects</topic><topic>Hormone metabolism and regulation</topic><topic>Insulin-Like Growth Factor I - pharmacology</topic><topic>Kinetics</topic><topic>Luteinizing Hormone - pharmacology</topic><topic>Mammalian female genital system</topic><topic>Molecular Sequence Data</topic><topic>Polymerase Chain Reaction</topic><topic>Progesterone - biosynthesis</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - metabolism</topic><topic>Theca Cells - enzymology</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MAGOFFIN, D. A</creatorcontrib><creatorcontrib>WEITSMAN, S. R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MAGOFFIN, D. A</au><au>WEITSMAN, S. R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin-like growth factor-I stimulates the expression of 3 beta-hydroxysteroid dehydrogenase messenger ribonucleic acid in ovarian theca-interstitial cells</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>1993-05-01</date><risdate>1993</risdate><volume>48</volume><issue>5</issue><spage>1166</spage><epage>1173</epage><pages>1166-1173</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>Evidence accumulating in the literature supports the hypothesis that insulin-like growth factor-I (IGF-I) may play a role
in stimulating differentiation of the ovarian theca-interstitial cells (TIC) during early follicular development. IGF-I has
been shown to synergistically enhance the stimulation of androgen biosynthesis and to increase LH binding in TIC. The purpose
of the present studies was to examine the role of IGF-I in TIC differentiation by determining the effects of IGF-I on 3 beta-hydroxysteroid
dehydrogenase (3 beta-HSD) mRNA expression in TIC stimulated to differentiate in vitro. TIC were isolated from the ovaries
of hypophysectomized immature rats by Percoll gradient centrifugation and cultured in the presence and absence of LH and IGF-I
for up to 6 days. At various times cytoplasmic RNA was extracted from the TIC, and 3 beta-HSD mRNA was measured by specific
assay using reverse transcription followed by the polymerase chain reaction. Amplification of 3 beta-HSD mRNA using primers
designed to distinguish between the type I and type II 3 beta-HSD gene products revealed that the TIC expressed primarily
the type I gene. Increasing concentrations of LH (0-1 microgram/ml) stimulated a dose-related increase in 3 beta-HSD mRNA
that was approximately 3-fold at 100 ng/ml of LH. Addition of IGF-I (30 ng/ml) increased 3 beta-HSD mRNA approximately 2-fold
over TIC treated with LH alone.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>8386947</pmid><doi>10.1095/biolreprod48.5.1166</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | 3-Hydroxysteroid Dehydrogenases - genetics Animals Base Sequence Biological and medical sciences Cell Differentiation DNA Restriction Enzymes Female Fundamental and applied biological sciences. Psychology Gene Expression - drug effects Hormone metabolism and regulation Insulin-Like Growth Factor I - pharmacology Kinetics Luteinizing Hormone - pharmacology Mammalian female genital system Molecular Sequence Data Polymerase Chain Reaction Progesterone - biosynthesis Rats Rats, Sprague-Dawley RNA, Messenger - metabolism Theca Cells - enzymology Vertebrates: reproduction |
title | Insulin-like growth factor-I stimulates the expression of 3 beta-hydroxysteroid dehydrogenase messenger ribonucleic acid in ovarian theca-interstitial cells |
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