Quantitative evaluation of the cell cycle-related retinoblastoma protein and localization of Thy-1 differentiation protein and macrophages during follicular development and atresia, and in human corpora lutea
Ovarian follicular development is dependent on growth and differentiation of the oocyte, as well as the granulosa and theca cell layers. The majority of primary follicles in the adult human ovary are not growing, and most antral follicles undergo atresia. The mechanisms regulating follicular growth...
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creator | BUKOVSKY, A CAUDLE, M. R KEENAN, J. A WIMALASENA, J FOSTER, J. S VAN METER, S. E |
description | Ovarian follicular development is dependent on growth and differentiation of the oocyte, as well as the granulosa and theca
cell layers. The majority of primary follicles in the adult human ovary are not growing, and most antral follicles undergo
atresia. The mechanisms regulating follicular growth and differentiation are poorly understood. Expression of key regulatory
proteins in cells of certain follicles may be involved. We have studied the distribution of retinoblastoma protein (pRb),
a key cell cycle regulator, in human follicles and CL by quantitative immunohistochemistry. Recent studies suggest that high
nuclear concentrations of pRb are associated with the arrest of cell proliferation and the beginning of differentiation; during
advanced differentiation of cells pRb is markedly depleted or absent. We also studied follicular distribution of Thy-1 differentiation
protein, a morpho-regulatory molecule associated with cell differentiation, and the presence of macrophages. Macrophages have
been shown to stimulate steroidogenesis in granulosa cells in vitro, and they are required for release of Thy-1 differentiation
protein from vascular pericytes among granulosa cells in vivo. Our results indicate that oocytes in resting follicles exhibit
pRb in the nucleoli. During initiation of follicular growth, the pRb expression first extends over the oocyte nuclei and then
diminishes from both nuclei and nucleoli in preantral follicles. When the oocytes reach maximum size in small antral follicles,
the pRb expression is reestablished in oocyte nucleoli. In differentiating granulosa and theca cell layers of preantral and
small antral follicles, pRb expression is high, but it is low in growing large antral follicles. During CL development and
regression, pRb expression in the nuclei of granulosa lutein cells first increases and then decreases. Follicular development
is accompanied by the presence of Thy-1 differentiation protein and macrophages under the follicular basement membrane. In
growing large antral follicles, during the mid-follicular phase, larger macrophages exhibit physical contacts with granulosa
cells through the follicular basement membrane, and, during the late follicular phase, small dendritic macrophages can be
detected among granulosa cells, but not within the follicular antrum. Large antral follicles undergoing atresia exhibit strong
pRb expression in granulosa cells. This is accompanied by a lack of Thy-1 differentiation protein among granulosa |
doi_str_mv | 10.1095/biolreprod52.4.776 |
format | Article |
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cell layers. The majority of primary follicles in the adult human ovary are not growing, and most antral follicles undergo
atresia. The mechanisms regulating follicular growth and differentiation are poorly understood. Expression of key regulatory
proteins in cells of certain follicles may be involved. We have studied the distribution of retinoblastoma protein (pRb),
a key cell cycle regulator, in human follicles and CL by quantitative immunohistochemistry. Recent studies suggest that high
nuclear concentrations of pRb are associated with the arrest of cell proliferation and the beginning of differentiation; during
advanced differentiation of cells pRb is markedly depleted or absent. We also studied follicular distribution of Thy-1 differentiation
protein, a morpho-regulatory molecule associated with cell differentiation, and the presence of macrophages. Macrophages have
been shown to stimulate steroidogenesis in granulosa cells in vitro, and they are required for release of Thy-1 differentiation
protein from vascular pericytes among granulosa cells in vivo. Our results indicate that oocytes in resting follicles exhibit
pRb in the nucleoli. During initiation of follicular growth, the pRb expression first extends over the oocyte nuclei and then
diminishes from both nuclei and nucleoli in preantral follicles. When the oocytes reach maximum size in small antral follicles,
the pRb expression is reestablished in oocyte nucleoli. In differentiating granulosa and theca cell layers of preantral and
small antral follicles, pRb expression is high, but it is low in growing large antral follicles. During CL development and
regression, pRb expression in the nuclei of granulosa lutein cells first increases and then decreases. Follicular development
is accompanied by the presence of Thy-1 differentiation protein and macrophages under the follicular basement membrane. In
growing large antral follicles, during the mid-follicular phase, larger macrophages exhibit physical contacts with granulosa
cells through the follicular basement membrane, and, during the late follicular phase, small dendritic macrophages can be
detected among granulosa cells, but not within the follicular antrum. Large antral follicles undergoing atresia exhibit strong
pRb expression in granulosa cells. This is accompanied by a lack of Thy-1 differentiation protein among granulosa cells and
the occurrence of large phagocytic macrophages in the follicular antrum. This is the first report of pRb expression in the
human ovary.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod52.4.776</identifier><identifier>PMID: 7780000</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Biological and medical sciences ; Cell Cycle ; Cell Differentiation ; Corpus Luteum - physiology ; Epithelium - chemistry ; Female ; Fluorescent Antibody Technique ; Follicular Atresia ; Fundamental and applied biological sciences. Psychology ; Granulosa Cells - chemistry ; Humans ; Immunoenzyme Techniques ; Macrophages - physiology ; Mammalian female genital system ; Morphology. Physiology ; Ovarian Follicle - physiology ; Retinoblastoma Protein - analysis ; Theca Cells - chemistry ; Thy-1 Antigens - analysis ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 1995-04, Vol.52 (4), p.776-792</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3488771$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7780000$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BUKOVSKY, A</creatorcontrib><creatorcontrib>CAUDLE, M. R</creatorcontrib><creatorcontrib>KEENAN, J. A</creatorcontrib><creatorcontrib>WIMALASENA, J</creatorcontrib><creatorcontrib>FOSTER, J. S</creatorcontrib><creatorcontrib>VAN METER, S. E</creatorcontrib><title>Quantitative evaluation of the cell cycle-related retinoblastoma protein and localization of Thy-1 differentiation protein and macrophages during follicular development and atresia, and in human corpora lutea</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>Ovarian follicular development is dependent on growth and differentiation of the oocyte, as well as the granulosa and theca
cell layers. The majority of primary follicles in the adult human ovary are not growing, and most antral follicles undergo
atresia. The mechanisms regulating follicular growth and differentiation are poorly understood. Expression of key regulatory
proteins in cells of certain follicles may be involved. We have studied the distribution of retinoblastoma protein (pRb),
a key cell cycle regulator, in human follicles and CL by quantitative immunohistochemistry. Recent studies suggest that high
nuclear concentrations of pRb are associated with the arrest of cell proliferation and the beginning of differentiation; during
advanced differentiation of cells pRb is markedly depleted or absent. We also studied follicular distribution of Thy-1 differentiation
protein, a morpho-regulatory molecule associated with cell differentiation, and the presence of macrophages. Macrophages have
been shown to stimulate steroidogenesis in granulosa cells in vitro, and they are required for release of Thy-1 differentiation
protein from vascular pericytes among granulosa cells in vivo. Our results indicate that oocytes in resting follicles exhibit
pRb in the nucleoli. During initiation of follicular growth, the pRb expression first extends over the oocyte nuclei and then
diminishes from both nuclei and nucleoli in preantral follicles. When the oocytes reach maximum size in small antral follicles,
the pRb expression is reestablished in oocyte nucleoli. In differentiating granulosa and theca cell layers of preantral and
small antral follicles, pRb expression is high, but it is low in growing large antral follicles. During CL development and
regression, pRb expression in the nuclei of granulosa lutein cells first increases and then decreases. Follicular development
is accompanied by the presence of Thy-1 differentiation protein and macrophages under the follicular basement membrane. In
growing large antral follicles, during the mid-follicular phase, larger macrophages exhibit physical contacts with granulosa
cells through the follicular basement membrane, and, during the late follicular phase, small dendritic macrophages can be
detected among granulosa cells, but not within the follicular antrum. Large antral follicles undergoing atresia exhibit strong
pRb expression in granulosa cells. This is accompanied by a lack of Thy-1 differentiation protein among granulosa cells and
the occurrence of large phagocytic macrophages in the follicular antrum. This is the first report of pRb expression in the
human ovary.</description><subject>Biological and medical sciences</subject><subject>Cell Cycle</subject><subject>Cell Differentiation</subject><subject>Corpus Luteum - physiology</subject><subject>Epithelium - chemistry</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Follicular Atresia</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Granulosa Cells - chemistry</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Macrophages - physiology</subject><subject>Mammalian female genital system</subject><subject>Morphology. Physiology</subject><subject>Ovarian Follicle - physiology</subject><subject>Retinoblastoma Protein - analysis</subject><subject>Theca Cells - chemistry</subject><subject>Thy-1 Antigens - analysis</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkV2L1DAUhoMo67j6BwQhF-qVHdOkbdJLWfxYWFiE9bqcJqfTSNrUJJ1h9lf6kzbuDIs3-eB9znPICSFvS7YtWVt_7q13AZfgTc231VbK5hnZlDVvC8kb9ZxsGGNNIUQjXpJXMf5mrKwEFxfkQkqVM7Yhf3-uMCebINk9UtyDW_PRz9QPNI1INTpH9VE7LAI6SGhowGRn3zuIyU9Ac_uEdqYwG-q8Bmfvnwx347EoqbHDgAFzm1Pwf8UEOvhlhB1GatZg5x0dvHNWrw4CNbhH55cp1z7SkAJGC58eL9kwrhPMVPuw-ADUrQnhNXkxgIv45rxfkl_fvt5d_Shubr9fX325KUbe1KnApqzaUikwPTDOWskNKslw4AMwxZlSukSGygD0vGl7LnULxuSVs1r0UlySjydvfs2fFWPqJhv_TQtm9GvspBRcNkpk8N0ZXPsJTbcEO0E4ducvyPn7cw4xT28IMGsbnzBRKSVlmbEPJ2y0u_FgA3ZxAueyVHSHw6HmXZWVjXgARCSrFQ</recordid><startdate>19950401</startdate><enddate>19950401</enddate><creator>BUKOVSKY, A</creator><creator>CAUDLE, M. 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E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h265t-e6149188adba020972de870ef2fa082088c1e0e8daab269b27c9add7c92053b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Biological and medical sciences</topic><topic>Cell Cycle</topic><topic>Cell Differentiation</topic><topic>Corpus Luteum - physiology</topic><topic>Epithelium - chemistry</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Follicular Atresia</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Granulosa Cells - chemistry</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Macrophages - physiology</topic><topic>Mammalian female genital system</topic><topic>Morphology. Physiology</topic><topic>Ovarian Follicle - physiology</topic><topic>Retinoblastoma Protein - analysis</topic><topic>Theca Cells - chemistry</topic><topic>Thy-1 Antigens - analysis</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BUKOVSKY, A</creatorcontrib><creatorcontrib>CAUDLE, M. R</creatorcontrib><creatorcontrib>KEENAN, J. A</creatorcontrib><creatorcontrib>WIMALASENA, J</creatorcontrib><creatorcontrib>FOSTER, J. S</creatorcontrib><creatorcontrib>VAN METER, S. E</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>BUKOVSKY, A</au><au>CAUDLE, M. R</au><au>KEENAN, J. A</au><au>WIMALASENA, J</au><au>FOSTER, J. S</au><au>VAN METER, S. E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative evaluation of the cell cycle-related retinoblastoma protein and localization of Thy-1 differentiation protein and macrophages during follicular development and atresia, and in human corpora lutea</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>1995-04-01</date><risdate>1995</risdate><volume>52</volume><issue>4</issue><spage>776</spage><epage>792</epage><pages>776-792</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>Ovarian follicular development is dependent on growth and differentiation of the oocyte, as well as the granulosa and theca
cell layers. The majority of primary follicles in the adult human ovary are not growing, and most antral follicles undergo
atresia. The mechanisms regulating follicular growth and differentiation are poorly understood. Expression of key regulatory
proteins in cells of certain follicles may be involved. We have studied the distribution of retinoblastoma protein (pRb),
a key cell cycle regulator, in human follicles and CL by quantitative immunohistochemistry. Recent studies suggest that high
nuclear concentrations of pRb are associated with the arrest of cell proliferation and the beginning of differentiation; during
advanced differentiation of cells pRb is markedly depleted or absent. We also studied follicular distribution of Thy-1 differentiation
protein, a morpho-regulatory molecule associated with cell differentiation, and the presence of macrophages. Macrophages have
been shown to stimulate steroidogenesis in granulosa cells in vitro, and they are required for release of Thy-1 differentiation
protein from vascular pericytes among granulosa cells in vivo. Our results indicate that oocytes in resting follicles exhibit
pRb in the nucleoli. During initiation of follicular growth, the pRb expression first extends over the oocyte nuclei and then
diminishes from both nuclei and nucleoli in preantral follicles. When the oocytes reach maximum size in small antral follicles,
the pRb expression is reestablished in oocyte nucleoli. In differentiating granulosa and theca cell layers of preantral and
small antral follicles, pRb expression is high, but it is low in growing large antral follicles. During CL development and
regression, pRb expression in the nuclei of granulosa lutein cells first increases and then decreases. Follicular development
is accompanied by the presence of Thy-1 differentiation protein and macrophages under the follicular basement membrane. In
growing large antral follicles, during the mid-follicular phase, larger macrophages exhibit physical contacts with granulosa
cells through the follicular basement membrane, and, during the late follicular phase, small dendritic macrophages can be
detected among granulosa cells, but not within the follicular antrum. Large antral follicles undergoing atresia exhibit strong
pRb expression in granulosa cells. This is accompanied by a lack of Thy-1 differentiation protein among granulosa cells and
the occurrence of large phagocytic macrophages in the follicular antrum. This is the first report of pRb expression in the
human ovary.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>7780000</pmid><doi>10.1095/biolreprod52.4.776</doi><tpages>17</tpages></addata></record> |
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ispartof | Biology of reproduction, 1995-04, Vol.52 (4), p.776-792 |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Biological and medical sciences Cell Cycle Cell Differentiation Corpus Luteum - physiology Epithelium - chemistry Female Fluorescent Antibody Technique Follicular Atresia Fundamental and applied biological sciences. Psychology Granulosa Cells - chemistry Humans Immunoenzyme Techniques Macrophages - physiology Mammalian female genital system Morphology. Physiology Ovarian Follicle - physiology Retinoblastoma Protein - analysis Theca Cells - chemistry Thy-1 Antigens - analysis Vertebrates: reproduction |
title | Quantitative evaluation of the cell cycle-related retinoblastoma protein and localization of Thy-1 differentiation protein and macrophages during follicular development and atresia, and in human corpora lutea |
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