Expression of Human Factor Ⅸ cDNA in Mice by Implants of Genetically Modified Skin Fibroblasts From a Hemophilia B Patient

Double-copy retroviral vector containing human factor Ⅸ cDNA driven by human cytomegalovirus enhancer-promoter was constructed. The vector was introduced into the amphotropic packaging cell line PA317. The recombinant virus produced in PA317 was used to transduce skin fibroblasts from a hemophilia B...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:中国科学:化学英文版 1993 (9), p.1082-1092
1. Verfasser: 周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1092
container_issue 9
container_start_page 1082
container_title 中国科学:化学英文版
container_volume
creator 周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦
description Double-copy retroviral vector containing human factor Ⅸ cDNA driven by human cytomegalovirus enhancer-promoter was constructed. The vector was introduced into the amphotropic packaging cell line PA317. The recombinant virus produced in PA317 was used to transduce skin fibroblasts from a hemophilia B patient. The infected cells produced high levels of biologically active human factor Ⅸ at a rate of 3420 ng/10~6 cells/24 h. These cells were embedded in a collagen matrix and implanted into the peritoneal cavity or subcutaneous space of mice. It was demonstrated that human factor Ⅸ was produced by the implants for at least 12 days in vivo, reaching a peak of 105 ng/ml plasma. Over 90% of the protein was functionally active. This technique has the potential to be developed into a new approach for gene therapy for hemophilia B.
format Article
fullrecord <record><control><sourceid>chongqing</sourceid><recordid>TN_cdi_chongqing_primary_4001485534</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>4001485534</cqvip_id><sourcerecordid>4001485534</sourcerecordid><originalsourceid>FETCH-chongqing_primary_40014855343</originalsourceid><addsrcrecordid>eNqNys1qwkAUhuFBWlCs93DAdWBiEhOX_THGhaXQ7uVknOip85POTMGAW-_F6-qVNAUvoN_m_RbPgI3iYr6I4iLnd_2f52mUzxbxkE28_-T9koTP8mzEzstT66T3ZA3YBqpvjQZKFME6-LlcQby8PgIZ2JCQUHew1q1CE_wfXkkjAwlUqoON3VFDcgfvx16XVDtbK_Q9LJ3VgFBJbdsDKUJ4gjcMJE14YPcNKi8nt47ZtFx-PFeROFiz_yKz37aONLpum3Iep0WWJWnyP_ULFxZPyA</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Expression of Human Factor Ⅸ cDNA in Mice by Implants of Genetically Modified Skin Fibroblasts From a Hemophilia B Patient</title><source>Alma/SFX Local Collection</source><creator>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</creator><creatorcontrib>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</creatorcontrib><description>Double-copy retroviral vector containing human factor Ⅸ cDNA driven by human cytomegalovirus enhancer-promoter was constructed. The vector was introduced into the amphotropic packaging cell line PA317. The recombinant virus produced in PA317 was used to transduce skin fibroblasts from a hemophilia B patient. The infected cells produced high levels of biologically active human factor Ⅸ at a rate of 3420 ng/10~6 cells/24 h. These cells were embedded in a collagen matrix and implanted into the peritoneal cavity or subcutaneous space of mice. It was demonstrated that human factor Ⅸ was produced by the implants for at least 12 days in vivo, reaching a peak of 105 ng/ml plasma. Over 90% of the protein was functionally active. This technique has the potential to be developed into a new approach for gene therapy for hemophilia B.</description><identifier>ISSN: 1674-7291</identifier><identifier>EISSN: 1869-1870</identifier><language>eng</language><subject>expression ; factor ; gene ; retroviral ; therapy ; vector ; vivo</subject><ispartof>中国科学:化学英文版, 1993 (9), p.1082-1092</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/60113X/60113X.jpg</thumbnail><link.rule.ids>314,780,784,4024</link.rule.ids></links><search><creatorcontrib>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</creatorcontrib><title>Expression of Human Factor Ⅸ cDNA in Mice by Implants of Genetically Modified Skin Fibroblasts From a Hemophilia B Patient</title><title>中国科学:化学英文版</title><addtitle>SCIENCE CHINA Chemistry</addtitle><description>Double-copy retroviral vector containing human factor Ⅸ cDNA driven by human cytomegalovirus enhancer-promoter was constructed. The vector was introduced into the amphotropic packaging cell line PA317. The recombinant virus produced in PA317 was used to transduce skin fibroblasts from a hemophilia B patient. The infected cells produced high levels of biologically active human factor Ⅸ at a rate of 3420 ng/10~6 cells/24 h. These cells were embedded in a collagen matrix and implanted into the peritoneal cavity or subcutaneous space of mice. It was demonstrated that human factor Ⅸ was produced by the implants for at least 12 days in vivo, reaching a peak of 105 ng/ml plasma. Over 90% of the protein was functionally active. This technique has the potential to be developed into a new approach for gene therapy for hemophilia B.</description><subject>expression</subject><subject>factor</subject><subject>gene</subject><subject>retroviral</subject><subject>therapy</subject><subject>vector</subject><subject>vivo</subject><issn>1674-7291</issn><issn>1869-1870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNqNys1qwkAUhuFBWlCs93DAdWBiEhOX_THGhaXQ7uVknOip85POTMGAW-_F6-qVNAUvoN_m_RbPgI3iYr6I4iLnd_2f52mUzxbxkE28_-T9koTP8mzEzstT66T3ZA3YBqpvjQZKFME6-LlcQby8PgIZ2JCQUHew1q1CE_wfXkkjAwlUqoON3VFDcgfvx16XVDtbK_Q9LJ3VgFBJbdsDKUJ4gjcMJE14YPcNKi8nt47ZtFx-PFeROFiz_yKz37aONLpum3Iep0WWJWnyP_ULFxZPyA</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>~WA</scope></search><sort><creationdate>1993</creationdate><title>Expression of Human Factor Ⅸ cDNA in Mice by Implants of Genetically Modified Skin Fibroblasts From a Hemophilia B Patient</title><author>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-chongqing_primary_40014855343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>expression</topic><topic>factor</topic><topic>gene</topic><topic>retroviral</topic><topic>therapy</topic><topic>vector</topic><topic>vivo</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><jtitle>中国科学:化学英文版</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>周洁民 戴一凡 邱信芳 侯国英 Yoshioka Akira 薛京伦</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of Human Factor Ⅸ cDNA in Mice by Implants of Genetically Modified Skin Fibroblasts From a Hemophilia B Patient</atitle><jtitle>中国科学:化学英文版</jtitle><addtitle>SCIENCE CHINA Chemistry</addtitle><date>1993</date><risdate>1993</risdate><issue>9</issue><spage>1082</spage><epage>1092</epage><pages>1082-1092</pages><issn>1674-7291</issn><eissn>1869-1870</eissn><abstract>Double-copy retroviral vector containing human factor Ⅸ cDNA driven by human cytomegalovirus enhancer-promoter was constructed. The vector was introduced into the amphotropic packaging cell line PA317. The recombinant virus produced in PA317 was used to transduce skin fibroblasts from a hemophilia B patient. The infected cells produced high levels of biologically active human factor Ⅸ at a rate of 3420 ng/10~6 cells/24 h. These cells were embedded in a collagen matrix and implanted into the peritoneal cavity or subcutaneous space of mice. It was demonstrated that human factor Ⅸ was produced by the implants for at least 12 days in vivo, reaching a peak of 105 ng/ml plasma. Over 90% of the protein was functionally active. This technique has the potential to be developed into a new approach for gene therapy for hemophilia B.</abstract></addata></record>
fulltext fulltext
identifier ISSN: 1674-7291
ispartof 中国科学:化学英文版, 1993 (9), p.1082-1092
issn 1674-7291
1869-1870
language eng
recordid cdi_chongqing_primary_4001485534
source Alma/SFX Local Collection
subjects expression
factor
gene
retroviral
therapy
vector
vivo
title Expression of Human Factor Ⅸ cDNA in Mice by Implants of Genetically Modified Skin Fibroblasts From a Hemophilia B Patient
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-31T16%3A23%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-chongqing&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Expression%20of%20Human%20Factor%20%E2%85%A8%20cDNA%20in%20Mice%20by%20Implants%20of%20Genetically%20Modified%20Skin%20Fibroblasts%20From%20a%20Hemophilia%20B%20Patient&rft.jtitle=%E4%B8%AD%E5%9B%BD%E7%A7%91%E5%AD%A6%EF%BC%9A%E5%8C%96%E5%AD%A6%E8%8B%B1%E6%96%87%E7%89%88&rft.au=%E5%91%A8%E6%B4%81%E6%B0%91%20%E6%88%B4%E4%B8%80%E5%87%A1%20%E9%82%B1%E4%BF%A1%E8%8A%B3%20%E4%BE%AF%E5%9B%BD%E8%8B%B1%20Yoshioka%20Akira%20%E8%96%9B%E4%BA%AC%E4%BC%A6&rft.date=1993&rft.issue=9&rft.spage=1082&rft.epage=1092&rft.pages=1082-1092&rft.issn=1674-7291&rft.eissn=1869-1870&rft_id=info:doi/&rft_dat=%3Cchongqing%3E4001485534%3C/chongqing%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_cqvip_id=4001485534&rfr_iscdi=true