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Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion

Sustained delivery of small interfering RNA (siRNA) is a challenge in gene silencing for managing gene‐related disorders. Although nanoparticle‐mediated electrospun fibers enable sustainable gene silencing, low efficiency, loss of biological activity, toxicity issues, and complex electrospinning tec...

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Autores principales: Liu, Shen, Wu, Fei, Gu, Shanshan, Wu, Tianyi, Chen, Shun, Chen, Shuai, Wang, Chongyang, Huang, Guanlan, Jin, Tuo, Cui, Wenguo, Sarmento, Bruno, Deng, Lianfu, Fan, Cunyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343062/
https://www.ncbi.nlm.nih.gov/pubmed/30693181
http://dx.doi.org/10.1002/advs.201801217
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author Liu, Shen
Wu, Fei
Gu, Shanshan
Wu, Tianyi
Chen, Shun
Chen, Shuai
Wang, Chongyang
Huang, Guanlan
Jin, Tuo
Cui, Wenguo
Sarmento, Bruno
Deng, Lianfu
Fan, Cunyi
author_facet Liu, Shen
Wu, Fei
Gu, Shanshan
Wu, Tianyi
Chen, Shun
Chen, Shuai
Wang, Chongyang
Huang, Guanlan
Jin, Tuo
Cui, Wenguo
Sarmento, Bruno
Deng, Lianfu
Fan, Cunyi
author_sort Liu, Shen
collection PubMed
description Sustained delivery of small interfering RNA (siRNA) is a challenge in gene silencing for managing gene‐related disorders. Although nanoparticle‐mediated electrospun fibers enable sustainable gene silencing, low efficiency, loss of biological activity, toxicity issues, and complex electrospinning techniques are all bottlenecks of these systems. Preventing peritendinous adhesion is crucial for their successful use, which involves blocking cellular signaling via physical barriers. Here, a multifunctional, yet structurally simple, cationic 2,6‐pyridinedicarboxaldehyde‐polyethylenimine (PDA)‐mediated extracellular signal‐regulated kinase (ERK)2‐siRNA polymeric delivery system is reported, in the form of peritendinous antiadhesion electrospun poly‐l‐lactic acid/hyaluronan membranes (P/H), with the ability to perform sustained release of bioactive siRNA for long‐term prevention of adhesions and ERK2 silencing. After 4 days of culture, the cell area and proliferation rate of chicken embryonic fibroblasts on siRNA+PDA+P/H membrane are significantly less than those on P/H and siRNA+P/H membranes. The in vivo results of average optical density of collagen type III (Col III) and gene expression of ERK2 and its downstream SMAD3 in the siRNA+PDA+P/H group are less than those of P/H and siRNA+P/H groups. Consequently, siRNA+PDA+P/H electrospun membrane can protect the bioactivity of ERK2‐siRNA and release it in a sustained manner. Moreover, adhesion formation is inhibited by reducing fibroblast proliferation and Col III deposition, and downregulating ERK2 and its downstream SMAD3.
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spelling pubmed-63430622019-01-28 Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion Liu, Shen Wu, Fei Gu, Shanshan Wu, Tianyi Chen, Shun Chen, Shuai Wang, Chongyang Huang, Guanlan Jin, Tuo Cui, Wenguo Sarmento, Bruno Deng, Lianfu Fan, Cunyi Adv Sci (Weinh) Full Papers Sustained delivery of small interfering RNA (siRNA) is a challenge in gene silencing for managing gene‐related disorders. Although nanoparticle‐mediated electrospun fibers enable sustainable gene silencing, low efficiency, loss of biological activity, toxicity issues, and complex electrospinning techniques are all bottlenecks of these systems. Preventing peritendinous adhesion is crucial for their successful use, which involves blocking cellular signaling via physical barriers. Here, a multifunctional, yet structurally simple, cationic 2,6‐pyridinedicarboxaldehyde‐polyethylenimine (PDA)‐mediated extracellular signal‐regulated kinase (ERK)2‐siRNA polymeric delivery system is reported, in the form of peritendinous antiadhesion electrospun poly‐l‐lactic acid/hyaluronan membranes (P/H), with the ability to perform sustained release of bioactive siRNA for long‐term prevention of adhesions and ERK2 silencing. After 4 days of culture, the cell area and proliferation rate of chicken embryonic fibroblasts on siRNA+PDA+P/H membrane are significantly less than those on P/H and siRNA+P/H membranes. The in vivo results of average optical density of collagen type III (Col III) and gene expression of ERK2 and its downstream SMAD3 in the siRNA+PDA+P/H group are less than those of P/H and siRNA+P/H groups. Consequently, siRNA+PDA+P/H electrospun membrane can protect the bioactivity of ERK2‐siRNA and release it in a sustained manner. Moreover, adhesion formation is inhibited by reducing fibroblast proliferation and Col III deposition, and downregulating ERK2 and its downstream SMAD3. John Wiley and Sons Inc. 2018-11-20 /pmc/articles/PMC6343062/ /pubmed/30693181 http://dx.doi.org/10.1002/advs.201801217 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the 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 Full Papers
Liu, Shen
Wu, Fei
Gu, Shanshan
Wu, Tianyi
Chen, Shun
Chen, Shuai
Wang, Chongyang
Huang, Guanlan
Jin, Tuo
Cui, Wenguo
Sarmento, Bruno
Deng, Lianfu
Fan, Cunyi
Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion
title Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion
title_full Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion
title_fullStr Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion
title_full_unstemmed Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion
title_short Gene Silencing via PDA/ERK2‐siRNA‐Mediated Electrospun Fibers for Peritendinous Antiadhesion
title_sort gene silencing via pda/erk2‐sirna‐mediated electrospun fibers for peritendinous antiadhesion
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343062/
https://www.ncbi.nlm.nih.gov/pubmed/30693181
http://dx.doi.org/10.1002/advs.201801217
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