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Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis

Mesenchymal stem cells (MSCs) have multiple properties including anti-inflammatory and immunomodulatory effects in various disease models and clinical treatments. These beneficial effects, however, are sometimes inconsistent and unpredictable. For wider and proper application, scientists sought to i...

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Autores principales: Park, Narae, Rim, Yeri Alice, Jung, Hyerin, Kim, Juryun, Yi, Hyoju, Kim, Youngkyun, Jang, Yeonsue, Jung, Seung Min, Lee, Jennifer, Kwok, Seung-Ki, Park, Sung-Hwan, Ju, Ji Hyeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234034/
https://www.ncbi.nlm.nih.gov/pubmed/28084468
http://dx.doi.org/10.1038/srep39593
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author Park, Narae
Rim, Yeri Alice
Jung, Hyerin
Kim, Juryun
Yi, Hyoju
Kim, Youngkyun
Jang, Yeonsue
Jung, Seung Min
Lee, Jennifer
Kwok, Seung-Ki
Park, Sung-Hwan
Ju, Ji Hyeon
author_facet Park, Narae
Rim, Yeri Alice
Jung, Hyerin
Kim, Juryun
Yi, Hyoju
Kim, Youngkyun
Jang, Yeonsue
Jung, Seung Min
Lee, Jennifer
Kwok, Seung-Ki
Park, Sung-Hwan
Ju, Ji Hyeon
author_sort Park, Narae
collection PubMed
description Mesenchymal stem cells (MSCs) have multiple properties including anti-inflammatory and immunomodulatory effects in various disease models and clinical treatments. These beneficial effects, however, are sometimes inconsistent and unpredictable. For wider and proper application, scientists sought to improve MSC functions by engineering. We aimed to invent a novel method to produce synthetic biological drugs from engineered MSCs. We investigated the anti-arthritic effect of engineered MSCs in a collagen-induced arthritis (CIA) model. Biologics such as etanercept are the most successful drugs used in anti-cytokine therapy. Biologics are made of protein components, and thus can be theoretically produced from cells including MSCs. MSCs were transfected with recombinant minicircles encoding etanercept (trade name, Enbrel), which is a tumour necrosis factor α blocker currently used to treat rheumatoid arthritis. We confirmed minicircle expression in MSCs in vitro based on GFP. Etanercept production was verified from the conditioned media. We confirmed that self-reproduced etanercept was biologically active in vitro. Arthritis subsided more efficiently in CIA mice injected with mcTNFR2MSCs than in those injected with conventional MSCs or etanercept only. Although this novel strategy is in a very early conceptual stage, it seems to represent a potential alternative method for the delivery of biologics and engineering MSCs.
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spelling pubmed-52340342017-01-18 Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis Park, Narae Rim, Yeri Alice Jung, Hyerin Kim, Juryun Yi, Hyoju Kim, Youngkyun Jang, Yeonsue Jung, Seung Min Lee, Jennifer Kwok, Seung-Ki Park, Sung-Hwan Ju, Ji Hyeon Sci Rep Article Mesenchymal stem cells (MSCs) have multiple properties including anti-inflammatory and immunomodulatory effects in various disease models and clinical treatments. These beneficial effects, however, are sometimes inconsistent and unpredictable. For wider and proper application, scientists sought to improve MSC functions by engineering. We aimed to invent a novel method to produce synthetic biological drugs from engineered MSCs. We investigated the anti-arthritic effect of engineered MSCs in a collagen-induced arthritis (CIA) model. Biologics such as etanercept are the most successful drugs used in anti-cytokine therapy. Biologics are made of protein components, and thus can be theoretically produced from cells including MSCs. MSCs were transfected with recombinant minicircles encoding etanercept (trade name, Enbrel), which is a tumour necrosis factor α blocker currently used to treat rheumatoid arthritis. We confirmed minicircle expression in MSCs in vitro based on GFP. Etanercept production was verified from the conditioned media. We confirmed that self-reproduced etanercept was biologically active in vitro. Arthritis subsided more efficiently in CIA mice injected with mcTNFR2MSCs than in those injected with conventional MSCs or etanercept only. Although this novel strategy is in a very early conceptual stage, it seems to represent a potential alternative method for the delivery of biologics and engineering MSCs. Nature Publishing Group 2017-01-13 /pmc/articles/PMC5234034/ /pubmed/28084468 http://dx.doi.org/10.1038/srep39593 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Park, Narae
Rim, Yeri Alice
Jung, Hyerin
Kim, Juryun
Yi, Hyoju
Kim, Youngkyun
Jang, Yeonsue
Jung, Seung Min
Lee, Jennifer
Kwok, Seung-Ki
Park, Sung-Hwan
Ju, Ji Hyeon
Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis
title Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis
title_full Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis
title_fullStr Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis
title_full_unstemmed Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis
title_short Etanercept-Synthesising Mesenchymal Stem Cells Efficiently Ameliorate Collagen-Induced Arthritis
title_sort etanercept-synthesising mesenchymal stem cells efficiently ameliorate collagen-induced arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234034/
https://www.ncbi.nlm.nih.gov/pubmed/28084468
http://dx.doi.org/10.1038/srep39593
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