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Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo

PDGF-CC is a member of the platelet-derived growth factor (PDGF) family that stimulates PDGFRα phosphorylation and thereby activates intracellular signalling events essential for development but also in cancer, fibrosis and neuropathologies involving blood-brain barrier (BBB) disruption. In order to...

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Autores principales: Li, Hong, Zeitelhofer, Manuel, Nilsson, Ingrid, Liu, Xicong, Allan, Laura, Gloria, Benjamin, Perani, Angelo, Murone, Carmel, Catimel, Bruno, Neville, A. Munro, Scott, Fiona E., Scott, Andrew M., Eriksson, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063412/
https://www.ncbi.nlm.nih.gov/pubmed/30052660
http://dx.doi.org/10.1371/journal.pone.0201089
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author Li, Hong
Zeitelhofer, Manuel
Nilsson, Ingrid
Liu, Xicong
Allan, Laura
Gloria, Benjamin
Perani, Angelo
Murone, Carmel
Catimel, Bruno
Neville, A. Munro
Scott, Fiona E.
Scott, Andrew M.
Eriksson, Ulf
author_facet Li, Hong
Zeitelhofer, Manuel
Nilsson, Ingrid
Liu, Xicong
Allan, Laura
Gloria, Benjamin
Perani, Angelo
Murone, Carmel
Catimel, Bruno
Neville, A. Munro
Scott, Fiona E.
Scott, Andrew M.
Eriksson, Ulf
author_sort Li, Hong
collection PubMed
description PDGF-CC is a member of the platelet-derived growth factor (PDGF) family that stimulates PDGFRα phosphorylation and thereby activates intracellular signalling events essential for development but also in cancer, fibrosis and neuropathologies involving blood-brain barrier (BBB) disruption. In order to elucidate the biological and pathological role(s) of PDGF-CC signalling, we have generated high affinity neutralizing monoclonal antibodies (mAbs) recognizing human PDGF-CC. We determined the complementarity determining regions (CDRs) of the selected clones, and mapped the binding epitope for clone 6B3. Using the monoclonal 6B3, we determined the expression pattern for PDGF-CC in different human primary tumours and control tissues, and explored its ability to neutralize PDGF-CC-induced phosphorylation of PDGFRα. In addition, we showed that PDGF-CC induced disruption of the blood-retinal barrier (BRB) was significantly reduced upon intraperitoneal administration of a chimeric anti-PDGF-CC antibody. In summary, we report on high affinity monoclonal antibodies against PDGF-CC that have therapeutic efficacy in vivo.
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spelling pubmed-60634122018-08-09 Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo Li, Hong Zeitelhofer, Manuel Nilsson, Ingrid Liu, Xicong Allan, Laura Gloria, Benjamin Perani, Angelo Murone, Carmel Catimel, Bruno Neville, A. Munro Scott, Fiona E. Scott, Andrew M. Eriksson, Ulf PLoS One Research Article PDGF-CC is a member of the platelet-derived growth factor (PDGF) family that stimulates PDGFRα phosphorylation and thereby activates intracellular signalling events essential for development but also in cancer, fibrosis and neuropathologies involving blood-brain barrier (BBB) disruption. In order to elucidate the biological and pathological role(s) of PDGF-CC signalling, we have generated high affinity neutralizing monoclonal antibodies (mAbs) recognizing human PDGF-CC. We determined the complementarity determining regions (CDRs) of the selected clones, and mapped the binding epitope for clone 6B3. Using the monoclonal 6B3, we determined the expression pattern for PDGF-CC in different human primary tumours and control tissues, and explored its ability to neutralize PDGF-CC-induced phosphorylation of PDGFRα. In addition, we showed that PDGF-CC induced disruption of the blood-retinal barrier (BRB) was significantly reduced upon intraperitoneal administration of a chimeric anti-PDGF-CC antibody. In summary, we report on high affinity monoclonal antibodies against PDGF-CC that have therapeutic efficacy in vivo. Public Library of Science 2018-07-27 /pmc/articles/PMC6063412/ /pubmed/30052660 http://dx.doi.org/10.1371/journal.pone.0201089 Text en © 2018 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Hong
Zeitelhofer, Manuel
Nilsson, Ingrid
Liu, Xicong
Allan, Laura
Gloria, Benjamin
Perani, Angelo
Murone, Carmel
Catimel, Bruno
Neville, A. Munro
Scott, Fiona E.
Scott, Andrew M.
Eriksson, Ulf
Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo
title Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo
title_full Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo
title_fullStr Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo
title_full_unstemmed Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo
title_short Development of monoclonal anti-PDGF-CC antibodies as tools for investigating human tissue expression and for blocking PDGF-CC induced PDGFRα signalling in vivo
title_sort development of monoclonal anti-pdgf-cc antibodies as tools for investigating human tissue expression and for blocking pdgf-cc induced pdgfrα signalling in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063412/
https://www.ncbi.nlm.nih.gov/pubmed/30052660
http://dx.doi.org/10.1371/journal.pone.0201089
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