Biodistribution of the RD114/mammalian type D retrovirus receptor, RDR

Background The limited expression of viral receptors on target cells is a recognized barrier to therapeutic gene transfer. Previous analysis of receptor expression has been performed using indirect methods due to a lack of receptor‐specific antibodies. Methods In this report we have used anti‐RDR an...

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Veröffentlicht in:The journal of gene medicine 2004-03, Vol.6 (3), p.249-259
Hauptverfasser: Green, Bronwyn J., Lee, C. Soon, Rasko, John E. J.
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Lee, C. Soon
Rasko, John E. J.
description Background The limited expression of viral receptors on target cells is a recognized barrier to therapeutic gene transfer. Previous analysis of receptor expression has been performed using indirect methods due to a lack of receptor‐specific antibodies. Methods In this report we have used anti‐RDR antiserum to provide direct histochemical and flow cytometric analysis of the expression of RDR, which is the cognate receptor for RD114‐pseudotyped vectors as well as being a neutral amino acid transporter. Results RDR was present on a range of normal tissues with relevance to gene therapy including: colon, testis, ovary, bone marrow and skeletal muscle. It was also highly expressed on immature cells present in the squamous epithelia of skin, cervix, nasal mucosa, bronchus and tonsil. Of relevance to possible germline gene transfer, we demonstrated a lack of RDR expression on male or female germ cells. RDR expression on mature hemopoietic cell subsets showed up to 5‐fold variability between individuals within each lineage—with some individuals expressing low levels of RDR across all blood lineages. Both myeloid and monocytic lineages contained the highest fraction of cells expressing RDR, whereas lymphoid lineages showed the lowest. Coexpression of CD34 and RDR ranged from 2.04 to 0.44% in G‐CSF‐mobilized peripheral blood samples. Conclusions As a means to optimize gene transfer protocols, biodistribution studies such as these are fundamental to enable targeting of the virus receptor most abundantly expressed on relevant populations. The inter‐individual variation of receptor expression seen here also raises the possible requirement for tailor‐made gene therapy protocols. Copyright © 2004 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/jgm.517
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Soon ; Rasko, John E. J.</creator><creatorcontrib>Green, Bronwyn J. ; Lee, C. Soon ; Rasko, John E. J.</creatorcontrib><description>Background The limited expression of viral receptors on target cells is a recognized barrier to therapeutic gene transfer. Previous analysis of receptor expression has been performed using indirect methods due to a lack of receptor‐specific antibodies. Methods In this report we have used anti‐RDR antiserum to provide direct histochemical and flow cytometric analysis of the expression of RDR, which is the cognate receptor for RD114‐pseudotyped vectors as well as being a neutral amino acid transporter. Results RDR was present on a range of normal tissues with relevance to gene therapy including: colon, testis, ovary, bone marrow and skeletal muscle. It was also highly expressed on immature cells present in the squamous epithelia of skin, cervix, nasal mucosa, bronchus and tonsil. Of relevance to possible germline gene transfer, we demonstrated a lack of RDR expression on male or female germ cells. RDR expression on mature hemopoietic cell subsets showed up to 5‐fold variability between individuals within each lineage—with some individuals expressing low levels of RDR across all blood lineages. Both myeloid and monocytic lineages contained the highest fraction of cells expressing RDR, whereas lymphoid lineages showed the lowest. Coexpression of CD34 and RDR ranged from 2.04 to 0.44% in G‐CSF‐mobilized peripheral blood samples. Conclusions As a means to optimize gene transfer protocols, biodistribution studies such as these are fundamental to enable targeting of the virus receptor most abundantly expressed on relevant populations. The inter‐individual variation of receptor expression seen here also raises the possible requirement for tailor‐made gene therapy protocols. Copyright © 2004 John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 1099-498X</identifier><identifier>EISSN: 1521-2254</identifier><identifier>DOI: 10.1002/jgm.517</identifier><identifier>PMID: 15026986</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>3T3 Cells ; Amino Acid Transport System ASC - immunology ; Amino Acid Transport System ASC - metabolism ; Animals ; Antigens, CD - immunology ; Antigens, CD - metabolism ; Betaretrovirus - genetics ; biodistribution ; Colon - metabolism ; Flow Cytometry ; Gene therapy ; Genetic Therapy ; Genetic Vectors - genetics ; Gonads - metabolism ; Hematopoietic System - metabolism ; Humans ; Immunoenzyme Techniques ; Immunohistochemistry ; Mice ; Minor Histocompatibility Antigens ; Muscle, Skeletal - metabolism ; Nasal Mucosa - metabolism ; RD114 retrovirus ; RDR ; retrovirus receptor ; Skin - metabolism</subject><ispartof>The journal of gene medicine, 2004-03, Vol.6 (3), p.249-259</ispartof><rights>Copyright © 2004 John Wiley &amp; Sons, Ltd.</rights><rights>Copyright 2004 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4757-6a46e123f30afb6bfdafeb318903c1f2fa493ebab344ede342ba352730a015a93</citedby><cites>FETCH-LOGICAL-c4757-6a46e123f30afb6bfdafeb318903c1f2fa493ebab344ede342ba352730a015a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjgm.517$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjgm.517$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15026986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Green, Bronwyn J.</creatorcontrib><creatorcontrib>Lee, C. Soon</creatorcontrib><creatorcontrib>Rasko, John E. J.</creatorcontrib><title>Biodistribution of the RD114/mammalian type D retrovirus receptor, RDR</title><title>The journal of gene medicine</title><addtitle>J. Gene Med</addtitle><description>Background The limited expression of viral receptors on target cells is a recognized barrier to therapeutic gene transfer. Previous analysis of receptor expression has been performed using indirect methods due to a lack of receptor‐specific antibodies. Methods In this report we have used anti‐RDR antiserum to provide direct histochemical and flow cytometric analysis of the expression of RDR, which is the cognate receptor for RD114‐pseudotyped vectors as well as being a neutral amino acid transporter. Results RDR was present on a range of normal tissues with relevance to gene therapy including: colon, testis, ovary, bone marrow and skeletal muscle. It was also highly expressed on immature cells present in the squamous epithelia of skin, cervix, nasal mucosa, bronchus and tonsil. Of relevance to possible germline gene transfer, we demonstrated a lack of RDR expression on male or female germ cells. RDR expression on mature hemopoietic cell subsets showed up to 5‐fold variability between individuals within each lineage—with some individuals expressing low levels of RDR across all blood lineages. Both myeloid and monocytic lineages contained the highest fraction of cells expressing RDR, whereas lymphoid lineages showed the lowest. Coexpression of CD34 and RDR ranged from 2.04 to 0.44% in G‐CSF‐mobilized peripheral blood samples. Conclusions As a means to optimize gene transfer protocols, biodistribution studies such as these are fundamental to enable targeting of the virus receptor most abundantly expressed on relevant populations. The inter‐individual variation of receptor expression seen here also raises the possible requirement for tailor‐made gene therapy protocols. 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Soon</au><au>Rasko, John E. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biodistribution of the RD114/mammalian type D retrovirus receptor, RDR</atitle><jtitle>The journal of gene medicine</jtitle><addtitle>J. Gene Med</addtitle><date>2004-03</date><risdate>2004</risdate><volume>6</volume><issue>3</issue><spage>249</spage><epage>259</epage><pages>249-259</pages><issn>1099-498X</issn><eissn>1521-2254</eissn><abstract>Background The limited expression of viral receptors on target cells is a recognized barrier to therapeutic gene transfer. Previous analysis of receptor expression has been performed using indirect methods due to a lack of receptor‐specific antibodies. Methods In this report we have used anti‐RDR antiserum to provide direct histochemical and flow cytometric analysis of the expression of RDR, which is the cognate receptor for RD114‐pseudotyped vectors as well as being a neutral amino acid transporter. Results RDR was present on a range of normal tissues with relevance to gene therapy including: colon, testis, ovary, bone marrow and skeletal muscle. It was also highly expressed on immature cells present in the squamous epithelia of skin, cervix, nasal mucosa, bronchus and tonsil. Of relevance to possible germline gene transfer, we demonstrated a lack of RDR expression on male or female germ cells. RDR expression on mature hemopoietic cell subsets showed up to 5‐fold variability between individuals within each lineage—with some individuals expressing low levels of RDR across all blood lineages. Both myeloid and monocytic lineages contained the highest fraction of cells expressing RDR, whereas lymphoid lineages showed the lowest. Coexpression of CD34 and RDR ranged from 2.04 to 0.44% in G‐CSF‐mobilized peripheral blood samples. Conclusions As a means to optimize gene transfer protocols, biodistribution studies such as these are fundamental to enable targeting of the virus receptor most abundantly expressed on relevant populations. The inter‐individual variation of receptor expression seen here also raises the possible requirement for tailor‐made gene therapy protocols. Copyright © 2004 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>15026986</pmid><doi>10.1002/jgm.517</doi><tpages>11</tpages></addata></record>
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subjects 3T3 Cells
Amino Acid Transport System ASC - immunology
Amino Acid Transport System ASC - metabolism
Animals
Antigens, CD - immunology
Antigens, CD - metabolism
Betaretrovirus - genetics
biodistribution
Colon - metabolism
Flow Cytometry
Gene therapy
Genetic Therapy
Genetic Vectors - genetics
Gonads - metabolism
Hematopoietic System - metabolism
Humans
Immunoenzyme Techniques
Immunohistochemistry
Mice
Minor Histocompatibility Antigens
Muscle, Skeletal - metabolism
Nasal Mucosa - metabolism
RD114 retrovirus
RDR
retrovirus receptor
Skin - metabolism
title Biodistribution of the RD114/mammalian type D retrovirus receptor, RDR
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