Cultivation and Characterization of BALB/cfC3H Mammary Tumor Cell Lines

Cell lines and sublines initiated from BALB/cfC3H mammary adenocarcinomas exhibited varying morphologies during the 15- to 21-month culture periods. Two epithelial cell lines, FUKU and MJY, continued to form the hemicysts and mounds characteristic of primary cell cultures. Subline MJY-alpha did not...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:JNCI : Journal of the National Cancer Institute 1973-12, Vol.51 (6), p.1849-1860
1. Verfasser: Yagi, M J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1860
container_issue 6
container_start_page 1849
container_title JNCI : Journal of the National Cancer Institute
container_volume 51
creator Yagi, M J
description Cell lines and sublines initiated from BALB/cfC3H mammary adenocarcinomas exhibited varying morphologies during the 15- to 21-month culture periods. Two epithelial cell lines, FUKU and MJY, continued to form the hemicysts and mounds characteristic of primary cell cultures. Subline MJY-alpha did not form these structures. Instead, the cells varied from polygonal to fusiform within each passage level and, when confluent, the monolayers continually released viable cells into the culture fluid. When introduced into isogeneic hosts, FUKU rapidly established adenocarcinomas with acinar areas, though MJY-alpha yielded only slow-growing carcinosarcomas. 3H-uridine incorporation revealed the constant release of virions from the cell lines and subline. Immunodiffusion assays of virus purified from the culture fluids indicated that FUKU released a mixture of virions containing both mammary tumor virus (MTV) and murine leukemia virus (MuLV) antigens; MJY-alpha virions, on the other hand, were positive for only MTV antigens. Electron microscopic examination of the cell lines and purified virions substantiated this finding. Immunofluorescence detected a shift in the localization of MTV antigens in fixed cell layers of long-term cultures. With increasing passage levels, the cytoplasmic fluorescence typical of primary cultures was replaced by a cell membrane-associated staining pattern. By the fourth to sixth passage level, only cell-surface fluorescence was observed with use of anti-MTV antisera.
doi_str_mv 10.1093/jnci/51.6.1849
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_82090778</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>82090778</sourcerecordid><originalsourceid>FETCH-LOGICAL-i244t-4c451cb6c1603febdc76f9cbff942905a81d1fe479de16dc385db5b981f84f303</originalsourceid><addsrcrecordid>eNo9jz1PwzAYhC0EKqWwsiFlYktrx3Zsj22ABggfQ5EqFstxbOGSjxInCPj1BLXille65_TqDoBzBKcICjzb1NrNKJrGU8SJOABjRGIYRgjSQzCGMGIh54wcgxPvN3CQiMgIjAimHBE6BsukLzv3qTrX1IGqiyB5U63SnWndz85sbLCYZ4uZtglOgwdVVar9DlZ91bRBYsoyyFxt_Ck4sqr05mx_J-Dl5nqVpGH2tLxN5lnoIkK6kGhCkc5jjWKIrckLzWIrdG6tIJGAVHFUIGsIE4VBcaExp0VOc8GR5cRiiCfgcvd32zYfvfGdrJzXQw1Vm6b3kkdQQMb4ELzYB_u8MoXctu6vuNwvH3i448535usfq_ZdxgwzKtP1q7xaP9L7xd2zTPEvvfNpVw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>82090778</pqid></control><display><type>article</type><title>Cultivation and Characterization of BALB/cfC3H Mammary Tumor Cell Lines</title><source>MEDLINE</source><source>Oxford University Press Archive</source><creator>Yagi, M J</creator><creatorcontrib>Yagi, M J</creatorcontrib><description>Cell lines and sublines initiated from BALB/cfC3H mammary adenocarcinomas exhibited varying morphologies during the 15- to 21-month culture periods. Two epithelial cell lines, FUKU and MJY, continued to form the hemicysts and mounds characteristic of primary cell cultures. Subline MJY-alpha did not form these structures. Instead, the cells varied from polygonal to fusiform within each passage level and, when confluent, the monolayers continually released viable cells into the culture fluid. When introduced into isogeneic hosts, FUKU rapidly established adenocarcinomas with acinar areas, though MJY-alpha yielded only slow-growing carcinosarcomas. 3H-uridine incorporation revealed the constant release of virions from the cell lines and subline. Immunodiffusion assays of virus purified from the culture fluids indicated that FUKU released a mixture of virions containing both mammary tumor virus (MTV) and murine leukemia virus (MuLV) antigens; MJY-alpha virions, on the other hand, were positive for only MTV antigens. Electron microscopic examination of the cell lines and purified virions substantiated this finding. Immunofluorescence detected a shift in the localization of MTV antigens in fixed cell layers of long-term cultures. With increasing passage levels, the cytoplasmic fluorescence typical of primary cultures was replaced by a cell membrane-associated staining pattern. By the fourth to sixth passage level, only cell-surface fluorescence was observed with use of anti-MTV antisera.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/51.6.1849</identifier><identifier>PMID: 4358145</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adenocarcinoma - immunology ; Adenocarcinoma - microbiology ; Adenocarcinoma - pathology ; Animals ; Antigens, Viral - analysis ; Cell Line ; Cell Membrane - immunology ; Cytoplasm - immunology ; Female ; Fluorescent Antibody Technique ; Immunodiffusion ; Leukemia Virus, Murine - immunology ; Leukemia Virus, Murine - isolation &amp; purification ; Mammary Neoplasms, Experimental - immunology ; Mammary Neoplasms, Experimental - microbiology ; Mammary Neoplasms, Experimental - pathology ; Mammary Tumor Virus, Mouse - immunology ; Mammary Tumor Virus, Mouse - isolation &amp; purification ; Mice ; Mice, Inbred Strains ; Microscopy, Electron ; Neoplasm Transplantation ; Sarcoma, Experimental - etiology ; Transplantation, Homologous ; Tritium ; Uridine - metabolism ; Virus Replication</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1973-12, Vol.51 (6), p.1849-1860</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4358145$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yagi, M J</creatorcontrib><title>Cultivation and Characterization of BALB/cfC3H Mammary Tumor Cell Lines</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>Journal of the National Cancer Institute</addtitle><description>Cell lines and sublines initiated from BALB/cfC3H mammary adenocarcinomas exhibited varying morphologies during the 15- to 21-month culture periods. Two epithelial cell lines, FUKU and MJY, continued to form the hemicysts and mounds characteristic of primary cell cultures. Subline MJY-alpha did not form these structures. Instead, the cells varied from polygonal to fusiform within each passage level and, when confluent, the monolayers continually released viable cells into the culture fluid. When introduced into isogeneic hosts, FUKU rapidly established adenocarcinomas with acinar areas, though MJY-alpha yielded only slow-growing carcinosarcomas. 3H-uridine incorporation revealed the constant release of virions from the cell lines and subline. Immunodiffusion assays of virus purified from the culture fluids indicated that FUKU released a mixture of virions containing both mammary tumor virus (MTV) and murine leukemia virus (MuLV) antigens; MJY-alpha virions, on the other hand, were positive for only MTV antigens. Electron microscopic examination of the cell lines and purified virions substantiated this finding. Immunofluorescence detected a shift in the localization of MTV antigens in fixed cell layers of long-term cultures. With increasing passage levels, the cytoplasmic fluorescence typical of primary cultures was replaced by a cell membrane-associated staining pattern. By the fourth to sixth passage level, only cell-surface fluorescence was observed with use of anti-MTV antisera.</description><subject>Adenocarcinoma - immunology</subject><subject>Adenocarcinoma - microbiology</subject><subject>Adenocarcinoma - pathology</subject><subject>Animals</subject><subject>Antigens, Viral - analysis</subject><subject>Cell Line</subject><subject>Cell Membrane - immunology</subject><subject>Cytoplasm - immunology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Immunodiffusion</subject><subject>Leukemia Virus, Murine - immunology</subject><subject>Leukemia Virus, Murine - isolation &amp; purification</subject><subject>Mammary Neoplasms, Experimental - immunology</subject><subject>Mammary Neoplasms, Experimental - microbiology</subject><subject>Mammary Neoplasms, Experimental - pathology</subject><subject>Mammary Tumor Virus, Mouse - immunology</subject><subject>Mammary Tumor Virus, Mouse - isolation &amp; purification</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Microscopy, Electron</subject><subject>Neoplasm Transplantation</subject><subject>Sarcoma, Experimental - etiology</subject><subject>Transplantation, Homologous</subject><subject>Tritium</subject><subject>Uridine - metabolism</subject><subject>Virus Replication</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9jz1PwzAYhC0EKqWwsiFlYktrx3Zsj22ABggfQ5EqFstxbOGSjxInCPj1BLXille65_TqDoBzBKcICjzb1NrNKJrGU8SJOABjRGIYRgjSQzCGMGIh54wcgxPvN3CQiMgIjAimHBE6BsukLzv3qTrX1IGqiyB5U63SnWndz85sbLCYZ4uZtglOgwdVVar9DlZ91bRBYsoyyFxt_Ck4sqr05mx_J-Dl5nqVpGH2tLxN5lnoIkK6kGhCkc5jjWKIrckLzWIrdG6tIJGAVHFUIGsIE4VBcaExp0VOc8GR5cRiiCfgcvd32zYfvfGdrJzXQw1Vm6b3kkdQQMb4ELzYB_u8MoXctu6vuNwvH3i448535usfq_ZdxgwzKtP1q7xaP9L7xd2zTPEvvfNpVw</recordid><startdate>197312</startdate><enddate>197312</enddate><creator>Yagi, M J</creator><general>Oxford University Press</general><scope>BSCLL</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>197312</creationdate><title>Cultivation and Characterization of BALB/cfC3H Mammary Tumor Cell Lines</title><author>Yagi, M J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i244t-4c451cb6c1603febdc76f9cbff942905a81d1fe479de16dc385db5b981f84f303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><topic>Adenocarcinoma - immunology</topic><topic>Adenocarcinoma - microbiology</topic><topic>Adenocarcinoma - pathology</topic><topic>Animals</topic><topic>Antigens, Viral - analysis</topic><topic>Cell Line</topic><topic>Cell Membrane - immunology</topic><topic>Cytoplasm - immunology</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Immunodiffusion</topic><topic>Leukemia Virus, Murine - immunology</topic><topic>Leukemia Virus, Murine - isolation &amp; purification</topic><topic>Mammary Neoplasms, Experimental - immunology</topic><topic>Mammary Neoplasms, Experimental - microbiology</topic><topic>Mammary Neoplasms, Experimental - pathology</topic><topic>Mammary Tumor Virus, Mouse - immunology</topic><topic>Mammary Tumor Virus, Mouse - isolation &amp; purification</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Microscopy, Electron</topic><topic>Neoplasm Transplantation</topic><topic>Sarcoma, Experimental - etiology</topic><topic>Transplantation, Homologous</topic><topic>Tritium</topic><topic>Uridine - metabolism</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yagi, M J</creatorcontrib><collection>Istex</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>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yagi, M J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cultivation and Characterization of BALB/cfC3H Mammary Tumor Cell Lines</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>Journal of the National Cancer Institute</addtitle><date>1973-12</date><risdate>1973</risdate><volume>51</volume><issue>6</issue><spage>1849</spage><epage>1860</epage><pages>1849-1860</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>Cell lines and sublines initiated from BALB/cfC3H mammary adenocarcinomas exhibited varying morphologies during the 15- to 21-month culture periods. Two epithelial cell lines, FUKU and MJY, continued to form the hemicysts and mounds characteristic of primary cell cultures. Subline MJY-alpha did not form these structures. Instead, the cells varied from polygonal to fusiform within each passage level and, when confluent, the monolayers continually released viable cells into the culture fluid. When introduced into isogeneic hosts, FUKU rapidly established adenocarcinomas with acinar areas, though MJY-alpha yielded only slow-growing carcinosarcomas. 3H-uridine incorporation revealed the constant release of virions from the cell lines and subline. Immunodiffusion assays of virus purified from the culture fluids indicated that FUKU released a mixture of virions containing both mammary tumor virus (MTV) and murine leukemia virus (MuLV) antigens; MJY-alpha virions, on the other hand, were positive for only MTV antigens. Electron microscopic examination of the cell lines and purified virions substantiated this finding. Immunofluorescence detected a shift in the localization of MTV antigens in fixed cell layers of long-term cultures. With increasing passage levels, the cytoplasmic fluorescence typical of primary cultures was replaced by a cell membrane-associated staining pattern. By the fourth to sixth passage level, only cell-surface fluorescence was observed with use of anti-MTV antisera.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>4358145</pmid><doi>10.1093/jnci/51.6.1849</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0027-8874
ispartof JNCI : Journal of the National Cancer Institute, 1973-12, Vol.51 (6), p.1849-1860
issn 0027-8874
1460-2105
language eng
recordid cdi_proquest_miscellaneous_82090778
source MEDLINE; Oxford University Press Archive
subjects Adenocarcinoma - immunology
Adenocarcinoma - microbiology
Adenocarcinoma - pathology
Animals
Antigens, Viral - analysis
Cell Line
Cell Membrane - immunology
Cytoplasm - immunology
Female
Fluorescent Antibody Technique
Immunodiffusion
Leukemia Virus, Murine - immunology
Leukemia Virus, Murine - isolation & purification
Mammary Neoplasms, Experimental - immunology
Mammary Neoplasms, Experimental - microbiology
Mammary Neoplasms, Experimental - pathology
Mammary Tumor Virus, Mouse - immunology
Mammary Tumor Virus, Mouse - isolation & purification
Mice
Mice, Inbred Strains
Microscopy, Electron
Neoplasm Transplantation
Sarcoma, Experimental - etiology
Transplantation, Homologous
Tritium
Uridine - metabolism
Virus Replication
title Cultivation and Characterization of BALB/cfC3H Mammary Tumor Cell Lines
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T04%3A23%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cultivation%20and%20Characterization%20of%20BALB/cfC3H%20Mammary%20Tumor%20Cell%20Lines&rft.jtitle=JNCI%20:%20Journal%20of%20the%20National%20Cancer%20Institute&rft.au=Yagi,%20M%20J&rft.date=1973-12&rft.volume=51&rft.issue=6&rft.spage=1849&rft.epage=1860&rft.pages=1849-1860&rft.issn=0027-8874&rft.eissn=1460-2105&rft_id=info:doi/10.1093/jnci/51.6.1849&rft_dat=%3Cproquest_pubme%3E82090778%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=82090778&rft_id=info:pmid/4358145&rfr_iscdi=true