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Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes

Implantation of peripheral blood aspirates induced towards chondrogenic differentiation upon genetic modification in sites of articular cartilage injury may represent a powerful strategy to enhance cartilage repair. Such a single‐step approach may be less invasive than procedures based on the use of...

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Autores principales: Frisch, Janina, Orth, Patrick, Rey‐Rico, Ana, Venkatesan, Jagadeesh Kumar, Schmitt, Gertrud, Madry, Henning, Kohn, Dieter, Cucchiarini, Magali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661259/
https://www.ncbi.nlm.nih.gov/pubmed/28467017
http://dx.doi.org/10.1111/jcmm.13190
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author Frisch, Janina
Orth, Patrick
Rey‐Rico, Ana
Venkatesan, Jagadeesh Kumar
Schmitt, Gertrud
Madry, Henning
Kohn, Dieter
Cucchiarini, Magali
author_facet Frisch, Janina
Orth, Patrick
Rey‐Rico, Ana
Venkatesan, Jagadeesh Kumar
Schmitt, Gertrud
Madry, Henning
Kohn, Dieter
Cucchiarini, Magali
author_sort Frisch, Janina
collection PubMed
description Implantation of peripheral blood aspirates induced towards chondrogenic differentiation upon genetic modification in sites of articular cartilage injury may represent a powerful strategy to enhance cartilage repair. Such a single‐step approach may be less invasive than procedures based on the use of isolated or concentrated MSCs, simplifying translational protocols in patients. In this study, we provide evidence showing the feasibility of overexpressing the mitogenic and pro‐anabolic insulin‐like growth factor I (IGF‐I) in human peripheral blood aspirates via rAAV‐mediated gene transfer, leading to enhanced proliferative and chondrogenic differentiation (proteoglycans, type‐II collagen, SOX9) activities in the samples relative to control (reporter rAAV‐lacZ) treatment over extended periods of time (at least 21 days, the longest time‐point evaluated). Interestingly, IGF‐I gene transfer also triggered hypertrophic, osteo‐ and adipogenic differentiation processes in the aspirates, suggesting that careful regulation of IGF‐I expression may be necessary to contain these events in vivo. Still, the current results demonstrate the potential of targeting human peripheral blood aspirates via therapeutic rAAV transduction as a novel, convenient tool to treat articular cartilage injuries.
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spelling pubmed-56612592017-11-02 Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes Frisch, Janina Orth, Patrick Rey‐Rico, Ana Venkatesan, Jagadeesh Kumar Schmitt, Gertrud Madry, Henning Kohn, Dieter Cucchiarini, Magali J Cell Mol Med Original Articles Implantation of peripheral blood aspirates induced towards chondrogenic differentiation upon genetic modification in sites of articular cartilage injury may represent a powerful strategy to enhance cartilage repair. Such a single‐step approach may be less invasive than procedures based on the use of isolated or concentrated MSCs, simplifying translational protocols in patients. In this study, we provide evidence showing the feasibility of overexpressing the mitogenic and pro‐anabolic insulin‐like growth factor I (IGF‐I) in human peripheral blood aspirates via rAAV‐mediated gene transfer, leading to enhanced proliferative and chondrogenic differentiation (proteoglycans, type‐II collagen, SOX9) activities in the samples relative to control (reporter rAAV‐lacZ) treatment over extended periods of time (at least 21 days, the longest time‐point evaluated). Interestingly, IGF‐I gene transfer also triggered hypertrophic, osteo‐ and adipogenic differentiation processes in the aspirates, suggesting that careful regulation of IGF‐I expression may be necessary to contain these events in vivo. Still, the current results demonstrate the potential of targeting human peripheral blood aspirates via therapeutic rAAV transduction as a novel, convenient tool to treat articular cartilage injuries. John Wiley and Sons Inc. 2017-05-03 2017-11 /pmc/articles/PMC5661259/ /pubmed/28467017 http://dx.doi.org/10.1111/jcmm.13190 Text en © 2017 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Frisch, Janina
Orth, Patrick
Rey‐Rico, Ana
Venkatesan, Jagadeesh Kumar
Schmitt, Gertrud
Madry, Henning
Kohn, Dieter
Cucchiarini, Magali
Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes
title Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes
title_full Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes
title_fullStr Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes
title_full_unstemmed Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes
title_short Peripheral blood aspirates overexpressing IGF‐I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes
title_sort peripheral blood aspirates overexpressing igf‐i via raav gene transfer undergo enhanced chondrogenic differentiation processes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661259/
https://www.ncbi.nlm.nih.gov/pubmed/28467017
http://dx.doi.org/10.1111/jcmm.13190
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