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Differences in gene expression profile among SH‐SY5Y neuroblastoma subclones with different neurite outgrowth responses to nerve growth factor
Nerve growth factor (NGF) plays a key role in the differentiation of neurons. In this study, we established three NGF‐induced neurite‐positive (NIN+) subclones that showed high responsiveness to NGF‐induced neurite outgrowth and three NGF‐induced neurite‐negative (NIN–) subclones that abolished NGF‐...
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Published in: | Journal of neurochemistry 2005-09, Vol.94 (5), p.1264-1276 |
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creator | Oe, Tomoya Sasayama, Takeshi Nagashima, Takeyuki Muramoto, Masakazu Yamazaki, Takao Morikawa, Noriyuki Okitsu, Osamau Nishimura, Shintaro Aoki, Toshiaki Katayama, Yoshiki Kita, Yasuhiro |
description | Nerve growth factor (NGF) plays a key role in the differentiation of neurons. In this study, we established three NGF‐induced neurite‐positive (NIN+) subclones that showed high responsiveness to NGF‐induced neurite outgrowth and three NGF‐induced neurite‐negative (NIN–) subclones that abolished NGF‐induced neurite outgrowth from parental SH‐SY5Y cells, and analyzed differences in the NGF signaling cascade. The NIN+ subclones showed enhanced responsiveness to FK506‐mediated neurite outgrowth as well. To clarify the mechanism behind the high frequency of NGF‐induced neurite outgrowth, we investigated differences in NGF signaling cascade among subclones. Expression levels of the NGF receptor TrkA, and NGF‐induced increases in mRNAs for the immediate‐early genes (IEGs) c‐fos and NGF inducible (NGFI) genes NGFI‐A, NGFI‐B and NGFI‐C, were identical among subclones. Microarray analysis revealed that the NIN+ cell line showed a very different gene expression profile to the NIN– cell line, particularly in terms of axonal vesicle‐related genes and growth cone guidance‐related genes. Thus, the difference in NGF signaling cascade between the NIN+ and NIN– cell lines was demonstrated by the difference in gene expression profile. These differentially expressed genes might play a key role in neurite outgrowth of SH‐SY5Y cells in a region downstream from the site of induction of IEGs, or in a novel NGF signaling cascade. |
doi_str_mv | 10.1111/j.1471-4159.2005.03273.x |
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In this study, we established three NGF‐induced neurite‐positive (NIN+) subclones that showed high responsiveness to NGF‐induced neurite outgrowth and three NGF‐induced neurite‐negative (NIN–) subclones that abolished NGF‐induced neurite outgrowth from parental SH‐SY5Y cells, and analyzed differences in the NGF signaling cascade. The NIN+ subclones showed enhanced responsiveness to FK506‐mediated neurite outgrowth as well. To clarify the mechanism behind the high frequency of NGF‐induced neurite outgrowth, we investigated differences in NGF signaling cascade among subclones. Expression levels of the NGF receptor TrkA, and NGF‐induced increases in mRNAs for the immediate‐early genes (IEGs) c‐fos and NGF inducible (NGFI) genes NGFI‐A, NGFI‐B and NGFI‐C, were identical among subclones. Microarray analysis revealed that the NIN+ cell line showed a very different gene expression profile to the NIN– cell line, particularly in terms of axonal vesicle‐related genes and growth cone guidance‐related genes. Thus, the difference in NGF signaling cascade between the NIN+ and NIN– cell lines was demonstrated by the difference in gene expression profile. These differentially expressed genes might play a key role in neurite outgrowth of SH‐SY5Y cells in a region downstream from the site of induction of IEGs, or in a novel NGF signaling cascade.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.2005.03273.x</identifier><identifier>PMID: 15992370</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Biochemistry ; Biological and medical sciences ; Cell Line, Tumor ; Clone Cells - metabolism ; Cloning ; Fundamental and applied biological sciences. Psychology ; Gene Expression ; Gene Expression Profiling ; Gene Expression Regulation - drug effects ; Genes, Immediate-Early ; high responsiveness ; Humans ; Isolated neuron and nerve. Neuroglia ; Medical sciences ; nerve growth factor ; Nerve Growth Factor - pharmacology ; neurite outgrowth ; Neurites - drug effects ; Neuroblastoma - genetics ; Neuroblastoma - metabolism ; Neuroblastoma - physiopathology ; Neurology ; Neurons ; Oligonucleotide Array Sequence Analysis ; Receptor, trkA - metabolism ; SH‐SY5Y neuroblastoma ; Signal transduction ; Tumors of the nervous system. Phacomatoses ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of neurochemistry, 2005-09, Vol.94 (5), p.1264-1276</ispartof><rights>2006 INIST-CNRS</rights><rights>2005 International Society for Neurochemistry</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4243-de88e08ca26275802b4092c2b5ed97f8fbc82d38b9237d573865a35aff5eb1a23</citedby><cites>FETCH-LOGICAL-c4243-de88e08ca26275802b4092c2b5ed97f8fbc82d38b9237d573865a35aff5eb1a23</cites></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=17019315$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15992370$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oe, Tomoya</creatorcontrib><creatorcontrib>Sasayama, Takeshi</creatorcontrib><creatorcontrib>Nagashima, Takeyuki</creatorcontrib><creatorcontrib>Muramoto, Masakazu</creatorcontrib><creatorcontrib>Yamazaki, Takao</creatorcontrib><creatorcontrib>Morikawa, Noriyuki</creatorcontrib><creatorcontrib>Okitsu, Osamau</creatorcontrib><creatorcontrib>Nishimura, Shintaro</creatorcontrib><creatorcontrib>Aoki, Toshiaki</creatorcontrib><creatorcontrib>Katayama, Yoshiki</creatorcontrib><creatorcontrib>Kita, Yasuhiro</creatorcontrib><title>Differences in gene expression profile among SH‐SY5Y neuroblastoma subclones with different neurite outgrowth responses to nerve growth factor</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>Nerve growth factor (NGF) plays a key role in the differentiation of neurons. In this study, we established three NGF‐induced neurite‐positive (NIN+) subclones that showed high responsiveness to NGF‐induced neurite outgrowth and three NGF‐induced neurite‐negative (NIN–) subclones that abolished NGF‐induced neurite outgrowth from parental SH‐SY5Y cells, and analyzed differences in the NGF signaling cascade. The NIN+ subclones showed enhanced responsiveness to FK506‐mediated neurite outgrowth as well. To clarify the mechanism behind the high frequency of NGF‐induced neurite outgrowth, we investigated differences in NGF signaling cascade among subclones. Expression levels of the NGF receptor TrkA, and NGF‐induced increases in mRNAs for the immediate‐early genes (IEGs) c‐fos and NGF inducible (NGFI) genes NGFI‐A, NGFI‐B and NGFI‐C, were identical among subclones. Microarray analysis revealed that the NIN+ cell line showed a very different gene expression profile to the NIN– cell line, particularly in terms of axonal vesicle‐related genes and growth cone guidance‐related genes. Thus, the difference in NGF signaling cascade between the NIN+ and NIN– cell lines was demonstrated by the difference in gene expression profile. These differentially expressed genes might play a key role in neurite outgrowth of SH‐SY5Y cells in a region downstream from the site of induction of IEGs, or in a novel NGF signaling cascade.</description><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Cell Line, Tumor</subject><subject>Clone Cells - metabolism</subject><subject>Cloning</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Genes, Immediate-Early</subject><subject>high responsiveness</subject><subject>Humans</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Medical sciences</subject><subject>nerve growth factor</subject><subject>Nerve Growth Factor - pharmacology</subject><subject>neurite outgrowth</subject><subject>Neurites - drug effects</subject><subject>Neuroblastoma - genetics</subject><subject>Neuroblastoma - metabolism</subject><subject>Neuroblastoma - physiopathology</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Receptor, trkA - metabolism</subject><subject>SH‐SY5Y neuroblastoma</subject><subject>Signal transduction</subject><subject>Tumors of the nervous system. Phacomatoses</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkc1u1DAURi0EotPCKyALCXYJ_okTZ8ECTYGCKlgUFl1ZjnM9ZJTYg50w010foc_Ik-B0Iiqxwhtb-o4_3auDEKYkp-m82ea0qGhWUFHnjBCRE84qnh8eodXf4DFaEcJYxknBTtBpjFtCaFmU9Ck6SXHNeEVW6O68sxYCOAMRdw5vwAGGwy5AjJ13eBe87XrAevBug68uft_eXV2La-xgCr7pdRz9oHGcGtN7lyr23fgDt0vneI91I2A_jZvg9ylLxTvvYkJHn-LwC_CSWG1GH56hJ1b3EZ4v9xn6_uH9t_VFdvn146f1u8vMFKzgWQtSApFGs5JVQhLWFKRmhjUC2rqy0jZGspbLZt6zFRWXpdBcaGsFNFQzfoZeH3vThj8niKMaumig77UDP0VVSkGEqEgCX_4Dbv0UXJpNMVKKQta1TJA8Qib4GANYtQvdoMONokTNytRWzWbUbEbNytS9MnVIX18s_VMzQPvwcXGUgFcLoKPRvQ3amS4-cBWhNacicW-P3D4Ju_nvAdTnL-v5xf8AluC1Yg</recordid><startdate>200509</startdate><enddate>200509</enddate><creator>Oe, Tomoya</creator><creator>Sasayama, Takeshi</creator><creator>Nagashima, Takeyuki</creator><creator>Muramoto, Masakazu</creator><creator>Yamazaki, Takao</creator><creator>Morikawa, Noriyuki</creator><creator>Okitsu, Osamau</creator><creator>Nishimura, Shintaro</creator><creator>Aoki, Toshiaki</creator><creator>Katayama, Yoshiki</creator><creator>Kita, Yasuhiro</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Blackwell Publishing Ltd</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200509</creationdate><title>Differences in gene expression profile among SH‐SY5Y neuroblastoma subclones with different neurite outgrowth responses to nerve growth factor</title><author>Oe, Tomoya ; Sasayama, Takeshi ; Nagashima, Takeyuki ; Muramoto, Masakazu ; Yamazaki, Takao ; Morikawa, Noriyuki ; Okitsu, Osamau ; Nishimura, Shintaro ; Aoki, Toshiaki ; Katayama, Yoshiki ; Kita, Yasuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4243-de88e08ca26275802b4092c2b5ed97f8fbc82d38b9237d573865a35aff5eb1a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Cell Line, Tumor</topic><topic>Clone Cells - metabolism</topic><topic>Cloning</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Genes, Immediate-Early</topic><topic>high responsiveness</topic><topic>Humans</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Medical sciences</topic><topic>nerve growth factor</topic><topic>Nerve Growth Factor - pharmacology</topic><topic>neurite outgrowth</topic><topic>Neurites - drug effects</topic><topic>Neuroblastoma - genetics</topic><topic>Neuroblastoma - metabolism</topic><topic>Neuroblastoma - physiopathology</topic><topic>Neurology</topic><topic>Neurons</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Receptor, trkA - metabolism</topic><topic>SH‐SY5Y neuroblastoma</topic><topic>Signal transduction</topic><topic>Tumors of the nervous system. Phacomatoses</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oe, Tomoya</creatorcontrib><creatorcontrib>Sasayama, Takeshi</creatorcontrib><creatorcontrib>Nagashima, Takeyuki</creatorcontrib><creatorcontrib>Muramoto, Masakazu</creatorcontrib><creatorcontrib>Yamazaki, Takao</creatorcontrib><creatorcontrib>Morikawa, Noriyuki</creatorcontrib><creatorcontrib>Okitsu, Osamau</creatorcontrib><creatorcontrib>Nishimura, Shintaro</creatorcontrib><creatorcontrib>Aoki, Toshiaki</creatorcontrib><creatorcontrib>Katayama, Yoshiki</creatorcontrib><creatorcontrib>Kita, Yasuhiro</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>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oe, Tomoya</au><au>Sasayama, Takeshi</au><au>Nagashima, Takeyuki</au><au>Muramoto, Masakazu</au><au>Yamazaki, Takao</au><au>Morikawa, Noriyuki</au><au>Okitsu, Osamau</au><au>Nishimura, Shintaro</au><au>Aoki, Toshiaki</au><au>Katayama, Yoshiki</au><au>Kita, Yasuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in gene expression profile among SH‐SY5Y neuroblastoma subclones with different neurite outgrowth responses to nerve growth factor</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2005-09</date><risdate>2005</risdate><volume>94</volume><issue>5</issue><spage>1264</spage><epage>1276</epage><pages>1264-1276</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>Nerve growth factor (NGF) plays a key role in the differentiation of neurons. In this study, we established three NGF‐induced neurite‐positive (NIN+) subclones that showed high responsiveness to NGF‐induced neurite outgrowth and three NGF‐induced neurite‐negative (NIN–) subclones that abolished NGF‐induced neurite outgrowth from parental SH‐SY5Y cells, and analyzed differences in the NGF signaling cascade. The NIN+ subclones showed enhanced responsiveness to FK506‐mediated neurite outgrowth as well. To clarify the mechanism behind the high frequency of NGF‐induced neurite outgrowth, we investigated differences in NGF signaling cascade among subclones. Expression levels of the NGF receptor TrkA, and NGF‐induced increases in mRNAs for the immediate‐early genes (IEGs) c‐fos and NGF inducible (NGFI) genes NGFI‐A, NGFI‐B and NGFI‐C, were identical among subclones. Microarray analysis revealed that the NIN+ cell line showed a very different gene expression profile to the NIN– cell line, particularly in terms of axonal vesicle‐related genes and growth cone guidance‐related genes. Thus, the difference in NGF signaling cascade between the NIN+ and NIN– cell lines was demonstrated by the difference in gene expression profile. These differentially expressed genes might play a key role in neurite outgrowth of SH‐SY5Y cells in a region downstream from the site of induction of IEGs, or in a novel NGF signaling cascade.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15992370</pmid><doi>10.1111/j.1471-4159.2005.03273.x</doi><tpages>13</tpages></addata></record> |
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subjects | Biochemistry Biological and medical sciences Cell Line, Tumor Clone Cells - metabolism Cloning Fundamental and applied biological sciences. Psychology Gene Expression Gene Expression Profiling Gene Expression Regulation - drug effects Genes, Immediate-Early high responsiveness Humans Isolated neuron and nerve. Neuroglia Medical sciences nerve growth factor Nerve Growth Factor - pharmacology neurite outgrowth Neurites - drug effects Neuroblastoma - genetics Neuroblastoma - metabolism Neuroblastoma - physiopathology Neurology Neurons Oligonucleotide Array Sequence Analysis Receptor, trkA - metabolism SH‐SY5Y neuroblastoma Signal transduction Tumors of the nervous system. Phacomatoses Vertebrates: nervous system and sense organs |
title | Differences in gene expression profile among SH‐SY5Y neuroblastoma subclones with different neurite outgrowth responses to nerve growth factor |
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