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Gene expression profiling of human erythroid progenitors by micro-serial analysis of gene expression
We compared the expression profiles of highly purified human CD34+ cells and erythroid progenitor cells by micro-serial analysis of gene expression (microSAGE). Human CD34+ cells were purified from granulocyte colony-stimulating factor-mobilized blood stem cells, and erythroid progenitors were obtai...
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Published in: | International journal of hematology 2004-10, Vol.80 (3), p.239-245 |
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container_title | International journal of hematology |
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creator | FUJISHIMA, Naohito HIROKAWA, Makoto AIBA, Namiko ICHIKAWA, Yoshikazu FUJISHIMA, Masumi KOMATSUDA, Atsushi SUZUKI, Yoshiko KAWABATA, Yoshinari MIURA, Ikuo SAWADA, Ken-Ichi |
description | We compared the expression profiles of highly purified human CD34+ cells and erythroid progenitor cells by micro-serial analysis of gene expression (microSAGE). Human CD34+ cells were purified from granulocyte colony-stimulating factor-mobilized blood stem cells, and erythroid progenitors were obtained by cultivating these cells in the presence of stem cell factor, interleukin 3, and erythropoietin. Our 10,202 SAGE tags allowed us to identify 1354 different transcripts appearing more than once. Erythroid progenitor cells showed increased expression of LRBA, EEF1A1, HSPCA, PILRB, RANBP1, NACA, and SMURF. Overexpression of HSPCA was confirmed by real-time polymerase chain reaction analysis. MicroSAGE revealed an unexpected preferential expression of several genes in erythroid progenitor cells in addition to the known functional genes, including hemoglobins. Our results provide reference data for future studies of gene expression in various hematopoietic disorders, including myelodysplastic syndrome and leukemia. |
doi_str_mv | 10.1532/IJH97.04053 |
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Human CD34+ cells were purified from granulocyte colony-stimulating factor-mobilized blood stem cells, and erythroid progenitors were obtained by cultivating these cells in the presence of stem cell factor, interleukin 3, and erythropoietin. Our 10,202 SAGE tags allowed us to identify 1354 different transcripts appearing more than once. Erythroid progenitor cells showed increased expression of LRBA, EEF1A1, HSPCA, PILRB, RANBP1, NACA, and SMURF. Overexpression of HSPCA was confirmed by real-time polymerase chain reaction analysis. MicroSAGE revealed an unexpected preferential expression of several genes in erythroid progenitor cells in addition to the known functional genes, including hemoglobins. Our results provide reference data for future studies of gene expression in various hematopoietic disorders, including myelodysplastic syndrome and leukemia.</description><identifier>ISSN: 0925-5710</identifier><identifier>EISSN: 1865-3774</identifier><identifier>DOI: 10.1532/IJH97.04053</identifier><identifier>PMID: 15540898</identifier><language>eng</language><publisher>Tokyo: Springer</publisher><subject>Antigens, CD34 ; Biological and medical sciences ; Cell Culture Techniques ; Cells, Cultured ; Erythroid Precursor Cells - metabolism ; Expressed Sequence Tags ; Gene Expression Profiling - methods ; Gene Library ; Hematologic and hematopoietic diseases ; Hematopoietic Stem Cells - metabolism ; Humans ; Medical sciences ; RNA, Messenger - analysis ; RNA, Messenger - standards</subject><ispartof>International journal of hematology, 2004-10, Vol.80 (3), p.239-245</ispartof><rights>2004 INIST-CNRS</rights><rights>The Japanese Society of Hematology 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-772814cdd1410d66f67cd59e525faf675025840a9c616da86577e1c347ed4b0f3</citedby><cites>FETCH-LOGICAL-c395t-772814cdd1410d66f67cd59e525faf675025840a9c616da86577e1c347ed4b0f3</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=16235135$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15540898$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FUJISHIMA, Naohito</creatorcontrib><creatorcontrib>HIROKAWA, Makoto</creatorcontrib><creatorcontrib>AIBA, Namiko</creatorcontrib><creatorcontrib>ICHIKAWA, Yoshikazu</creatorcontrib><creatorcontrib>FUJISHIMA, Masumi</creatorcontrib><creatorcontrib>KOMATSUDA, Atsushi</creatorcontrib><creatorcontrib>SUZUKI, Yoshiko</creatorcontrib><creatorcontrib>KAWABATA, Yoshinari</creatorcontrib><creatorcontrib>MIURA, Ikuo</creatorcontrib><creatorcontrib>SAWADA, Ken-Ichi</creatorcontrib><title>Gene expression profiling of human erythroid progenitors by micro-serial analysis of gene expression</title><title>International journal of hematology</title><addtitle>Int J Hematol</addtitle><description>We compared the expression profiles of highly purified human CD34+ cells and erythroid progenitor cells by micro-serial analysis of gene expression (microSAGE). Human CD34+ cells were purified from granulocyte colony-stimulating factor-mobilized blood stem cells, and erythroid progenitors were obtained by cultivating these cells in the presence of stem cell factor, interleukin 3, and erythropoietin. Our 10,202 SAGE tags allowed us to identify 1354 different transcripts appearing more than once. Erythroid progenitor cells showed increased expression of LRBA, EEF1A1, HSPCA, PILRB, RANBP1, NACA, and SMURF. Overexpression of HSPCA was confirmed by real-time polymerase chain reaction analysis. MicroSAGE revealed an unexpected preferential expression of several genes in erythroid progenitor cells in addition to the known functional genes, including hemoglobins. Our results provide reference data for future studies of gene expression in various hematopoietic disorders, including myelodysplastic syndrome and leukemia.</description><subject>Antigens, CD34</subject><subject>Biological and medical sciences</subject><subject>Cell Culture Techniques</subject><subject>Cells, Cultured</subject><subject>Erythroid Precursor Cells - metabolism</subject><subject>Expressed Sequence Tags</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Library</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematopoietic Stem Cells - metabolism</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - standards</subject><issn>0925-5710</issn><issn>1865-3774</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpdkEtLAzEURoMotlZX7mUQdCNTk8lrZilF20rBja6HNMm0KfOouR1w_r1pO1B0FS459-N-B6FbgseE0-R5_j7L5BgzzOkZGpJU8JhKyc7REGcJj7kkeICuADYYE4mZvEQDwjnDaZYOkZna2kb2Z-stgGvqaOubwpWuXkVNEa3bStWR9d1u7Rtn9p8rW7td4yFadlHltG9isN6pMlK1KjtwsN9b_Q29RheFKsHe9O8Ifb29fk5m8eJjOp-8LGJNM76LpUxSwrQxhBFshCiE1IZnlie8UGHgOOEpwyrTggijQlEpLdGUSWvYEhd0hB6PueHO79bCLq8caFuWqrZNC7mQWPA0EwG8_wdumtaHApAnRNJUpoIE6OkIhZIA3hb51rtK-S4nON-bzw_m84P5QN_1ke2ysubE9qoD8NADCrQqC69q7eDEiYRyQjn9BbAVi3I</recordid><startdate>20041001</startdate><enddate>20041001</enddate><creator>FUJISHIMA, Naohito</creator><creator>HIROKAWA, Makoto</creator><creator>AIBA, Namiko</creator><creator>ICHIKAWA, Yoshikazu</creator><creator>FUJISHIMA, Masumi</creator><creator>KOMATSUDA, Atsushi</creator><creator>SUZUKI, Yoshiko</creator><creator>KAWABATA, Yoshinari</creator><creator>MIURA, Ikuo</creator><creator>SAWADA, Ken-Ichi</creator><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20041001</creationdate><title>Gene expression profiling of human erythroid progenitors by micro-serial analysis of gene expression</title><author>FUJISHIMA, Naohito ; HIROKAWA, Makoto ; AIBA, Namiko ; ICHIKAWA, Yoshikazu ; FUJISHIMA, Masumi ; KOMATSUDA, Atsushi ; SUZUKI, Yoshiko ; KAWABATA, Yoshinari ; MIURA, Ikuo ; SAWADA, Ken-Ichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-772814cdd1410d66f67cd59e525faf675025840a9c616da86577e1c347ed4b0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Antigens, CD34</topic><topic>Biological and medical sciences</topic><topic>Cell Culture Techniques</topic><topic>Cells, Cultured</topic><topic>Erythroid Precursor Cells - metabolism</topic><topic>Expressed Sequence Tags</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Library</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hematopoietic Stem Cells - metabolism</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - standards</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FUJISHIMA, Naohito</creatorcontrib><creatorcontrib>HIROKAWA, Makoto</creatorcontrib><creatorcontrib>AIBA, Namiko</creatorcontrib><creatorcontrib>ICHIKAWA, Yoshikazu</creatorcontrib><creatorcontrib>FUJISHIMA, Masumi</creatorcontrib><creatorcontrib>KOMATSUDA, Atsushi</creatorcontrib><creatorcontrib>SUZUKI, Yoshiko</creatorcontrib><creatorcontrib>KAWABATA, Yoshinari</creatorcontrib><creatorcontrib>MIURA, Ikuo</creatorcontrib><creatorcontrib>SAWADA, Ken-Ichi</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>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FUJISHIMA, Naohito</au><au>HIROKAWA, Makoto</au><au>AIBA, Namiko</au><au>ICHIKAWA, Yoshikazu</au><au>FUJISHIMA, Masumi</au><au>KOMATSUDA, Atsushi</au><au>SUZUKI, Yoshiko</au><au>KAWABATA, Yoshinari</au><au>MIURA, Ikuo</au><au>SAWADA, Ken-Ichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene expression profiling of human erythroid progenitors by micro-serial analysis of gene expression</atitle><jtitle>International journal of hematology</jtitle><addtitle>Int J Hematol</addtitle><date>2004-10-01</date><risdate>2004</risdate><volume>80</volume><issue>3</issue><spage>239</spage><epage>245</epage><pages>239-245</pages><issn>0925-5710</issn><eissn>1865-3774</eissn><abstract>We compared the expression profiles of highly purified human CD34+ cells and erythroid progenitor cells by micro-serial analysis of gene expression (microSAGE). Human CD34+ cells were purified from granulocyte colony-stimulating factor-mobilized blood stem cells, and erythroid progenitors were obtained by cultivating these cells in the presence of stem cell factor, interleukin 3, and erythropoietin. Our 10,202 SAGE tags allowed us to identify 1354 different transcripts appearing more than once. Erythroid progenitor cells showed increased expression of LRBA, EEF1A1, HSPCA, PILRB, RANBP1, NACA, and SMURF. Overexpression of HSPCA was confirmed by real-time polymerase chain reaction analysis. MicroSAGE revealed an unexpected preferential expression of several genes in erythroid progenitor cells in addition to the known functional genes, including hemoglobins. Our results provide reference data for future studies of gene expression in various hematopoietic disorders, including myelodysplastic syndrome and leukemia.</abstract><cop>Tokyo</cop><pub>Springer</pub><pmid>15540898</pmid><doi>10.1532/IJH97.04053</doi><tpages>7</tpages></addata></record> |
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subjects | Antigens, CD34 Biological and medical sciences Cell Culture Techniques Cells, Cultured Erythroid Precursor Cells - metabolism Expressed Sequence Tags Gene Expression Profiling - methods Gene Library Hematologic and hematopoietic diseases Hematopoietic Stem Cells - metabolism Humans Medical sciences RNA, Messenger - analysis RNA, Messenger - standards |
title | Gene expression profiling of human erythroid progenitors by micro-serial analysis of gene expression |
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