Astrocytes enhance the invasion potential of glioblastoma stem-like cells
Glioblastomas (GBMs) are characterized as highly invasive; the contribution of GBM stem-like cells (GSCs) to the invasive phenotype, however, has not been completely defined. Towards this end, we have defined the invasion potential of CD133+ GSCs and their differentiated CD133- counterparts grown un...
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description | Glioblastomas (GBMs) are characterized as highly invasive; the contribution of GBM stem-like cells (GSCs) to the invasive phenotype, however, has not been completely defined. Towards this end, we have defined the invasion potential of CD133+ GSCs and their differentiated CD133- counterparts grown under standard in vitro conditions and in co-culture with astrocytes. Using a trans-well assay, astrocytes or astrocyte conditioned media in the bottom chamber significantly increased the invasion of GSCs yet had no effect on CD133- cells. In addition, a monolayer invasion assay showed that the GSCs invaded farther into an astrocyte monolayer than their differentiated progeny. Gene expression profiles were generated from two GSC lines grown in trans-well culture with astrocytes in the bottom chamber or directly in contact with astrocyte monolayers. In each co-culture model, genes whose expression was commonly increased in both GSC lines involved cell movement and included a number of genes that have been previously associated with tumor cell invasion. Similar gene expression modifications were not detected in CD133- cells co-cultured under the same conditions with astrocytes. Finally, evaluation of the secretome of astrocytes grown in monolayer identified a number of chemokines and cytokines associated with tumor cell invasion. These data suggest that astrocytes enhance the invasion of CD133+ GSCs and provide additional support for a critical role of brain microenvironment in the regulation of GBM biology. |
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Towards this end, we have defined the invasion potential of CD133+ GSCs and their differentiated CD133- counterparts grown under standard in vitro conditions and in co-culture with astrocytes. Using a trans-well assay, astrocytes or astrocyte conditioned media in the bottom chamber significantly increased the invasion of GSCs yet had no effect on CD133- cells. In addition, a monolayer invasion assay showed that the GSCs invaded farther into an astrocyte monolayer than their differentiated progeny. Gene expression profiles were generated from two GSC lines grown in trans-well culture with astrocytes in the bottom chamber or directly in contact with astrocyte monolayers. In each co-culture model, genes whose expression was commonly increased in both GSC lines involved cell movement and included a number of genes that have been previously associated with tumor cell invasion. Similar gene expression modifications were not detected in CD133- cells co-cultured under the same conditions with astrocytes. Finally, evaluation of the secretome of astrocytes grown in monolayer identified a number of chemokines and cytokines associated with tumor cell invasion. These data suggest that astrocytes enhance the invasion of CD133+ GSCs and provide additional support for a critical role of brain microenvironment in the regulation of GBM biology.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0054752</identifier><identifier>PMID: 23349962</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>AC133 Antigen ; Antigens, CD - metabolism ; Astrocytes ; Astrocytes - cytology ; Astrocytes - metabolism ; Biology ; Brain ; Brain cancer ; Brain Neoplasms - metabolism ; Brain Neoplasms - pathology ; Cancer therapies ; Cell culture ; Cell cycle ; Cell Differentiation ; Cell growth ; Cell Line, Tumor ; Chemokines ; Chemotherapy ; Conditioning ; Culture Media, Conditioned - metabolism ; Culture Media, Conditioned - pharmacology ; Cytokines ; Experiments ; Gene expression ; Genes ; Glioblastoma ; Glioblastoma - metabolism ; Glioblastoma - pathology ; Glycoproteins - metabolism ; Growth factors ; Humans ; Medicine ; Microscopy, Electron, Scanning Transmission ; Monolayers ; Monomolecular films ; Neoplasm Invasiveness - pathology ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Oncology ; Peptides - metabolism ; Progeny ; Radiation therapy ; Secretome ; Stem cells ; Transcriptome ; Tumor Microenvironment</subject><ispartof>PloS one, 2013-01, Vol.8 (1), p.e54752-e54752</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013. This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-5d37797b05e17adca83e75827e8d1358482ef59afff434d5f1b053209a6fac203</citedby><cites>FETCH-LOGICAL-c758t-5d37797b05e17adca83e75827e8d1358482ef59afff434d5f1b053209a6fac203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551925/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551925/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23349962$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Castro, Maria G.</contributor><creatorcontrib>Rath, Barbara H</creatorcontrib><creatorcontrib>Fair, Joshlean M</creatorcontrib><creatorcontrib>Jamal, Muhammad</creatorcontrib><creatorcontrib>Camphausen, Kevin</creatorcontrib><creatorcontrib>Tofilon, Philip J</creatorcontrib><title>Astrocytes enhance the invasion potential of glioblastoma stem-like cells</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Glioblastomas (GBMs) are characterized as highly invasive; the contribution of GBM stem-like cells (GSCs) to the invasive phenotype, however, has not been completely defined. Towards this end, we have defined the invasion potential of CD133+ GSCs and their differentiated CD133- counterparts grown under standard in vitro conditions and in co-culture with astrocytes. Using a trans-well assay, astrocytes or astrocyte conditioned media in the bottom chamber significantly increased the invasion of GSCs yet had no effect on CD133- cells. In addition, a monolayer invasion assay showed that the GSCs invaded farther into an astrocyte monolayer than their differentiated progeny. Gene expression profiles were generated from two GSC lines grown in trans-well culture with astrocytes in the bottom chamber or directly in contact with astrocyte monolayers. In each co-culture model, genes whose expression was commonly increased in both GSC lines involved cell movement and included a number of genes that have been previously associated with tumor cell invasion. Similar gene expression modifications were not detected in CD133- cells co-cultured under the same conditions with astrocytes. Finally, evaluation of the secretome of astrocytes grown in monolayer identified a number of chemokines and cytokines associated with tumor cell invasion. These data suggest that astrocytes enhance the invasion of CD133+ GSCs and provide additional support for a critical role of brain microenvironment in the regulation of GBM biology.</description><subject>AC133 Antigen</subject><subject>Antigens, CD - metabolism</subject><subject>Astrocytes</subject><subject>Astrocytes - cytology</subject><subject>Astrocytes - metabolism</subject><subject>Biology</subject><subject>Brain</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - metabolism</subject><subject>Brain Neoplasms - pathology</subject><subject>Cancer therapies</subject><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Cell Differentiation</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Chemokines</subject><subject>Chemotherapy</subject><subject>Conditioning</subject><subject>Culture Media, Conditioned - metabolism</subject><subject>Culture Media, Conditioned - pharmacology</subject><subject>Cytokines</subject><subject>Experiments</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Glioblastoma</subject><subject>Glioblastoma - 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Towards this end, we have defined the invasion potential of CD133+ GSCs and their differentiated CD133- counterparts grown under standard in vitro conditions and in co-culture with astrocytes. Using a trans-well assay, astrocytes or astrocyte conditioned media in the bottom chamber significantly increased the invasion of GSCs yet had no effect on CD133- cells. In addition, a monolayer invasion assay showed that the GSCs invaded farther into an astrocyte monolayer than their differentiated progeny. Gene expression profiles were generated from two GSC lines grown in trans-well culture with astrocytes in the bottom chamber or directly in contact with astrocyte monolayers. In each co-culture model, genes whose expression was commonly increased in both GSC lines involved cell movement and included a number of genes that have been previously associated with tumor cell invasion. Similar gene expression modifications were not detected in CD133- cells co-cultured under the same conditions with astrocytes. Finally, evaluation of the secretome of astrocytes grown in monolayer identified a number of chemokines and cytokines associated with tumor cell invasion. These data suggest that astrocytes enhance the invasion of CD133+ GSCs and provide additional support for a critical role of brain microenvironment in the regulation of GBM biology.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23349962</pmid><doi>10.1371/journal.pone.0054752</doi><tpages>e54752</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AC133 Antigen Antigens, CD - metabolism Astrocytes Astrocytes - cytology Astrocytes - metabolism Biology Brain Brain cancer Brain Neoplasms - metabolism Brain Neoplasms - pathology Cancer therapies Cell culture Cell cycle Cell Differentiation Cell growth Cell Line, Tumor Chemokines Chemotherapy Conditioning Culture Media, Conditioned - metabolism Culture Media, Conditioned - pharmacology Cytokines Experiments Gene expression Genes Glioblastoma Glioblastoma - metabolism Glioblastoma - pathology Glycoproteins - metabolism Growth factors Humans Medicine Microscopy, Electron, Scanning Transmission Monolayers Monomolecular films Neoplasm Invasiveness - pathology Neoplastic Stem Cells - metabolism Neoplastic Stem Cells - pathology Oncology Peptides - metabolism Progeny Radiation therapy Secretome Stem cells Transcriptome Tumor Microenvironment |
title | Astrocytes enhance the invasion potential of glioblastoma stem-like cells |
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