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

adhesion prevention adhesion tissue formation electrospun fibers gene delivery siRNA

Journal

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN: 2198-3844
Titre abrégé: Adv Sci (Weinh)
Pays: Germany
ID NLM: 101664569

Informations de publication

Date de publication:
23 Jan 2019
Historique:
received: 27 07 2018
revised: 30 09 2018
entrez: 30 1 2019
pubmed: 30 1 2019
medline: 30 1 2019
Statut: epublish

Résumé

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.

Identifiants

pubmed: 30693181
doi: 10.1002/advs.201801217
pii: ADVS870
pmc: PMC6343062
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1801217

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Auteurs

Shen Liu (S)

Department of Orthopaedics Shanghai Jiao Tong University Affiliated Sixth People's Hospital 600 Yishan Road Shanghai 200233 China.
Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 China.

Fei Wu (F)

School of Pharmacy Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China.

Shanshan Gu (S)

School of Pharmacy Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China.

Tianyi Wu (T)

Department of Orthopaedics Shanghai Jiao Tong University Affiliated Sixth People's Hospital 600 Yishan Road Shanghai 200233 China.

Shun Chen (S)

Department of Orthopaedics Shanghai Jiao Tong University Affiliated Sixth People's Hospital 600 Yishan Road Shanghai 200233 China.

Shuai Chen (S)

School of Pharmacy Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China.

Chongyang Wang (C)

Department of Orthopaedics Shanghai Jiao Tong University Affiliated Sixth People's Hospital 600 Yishan Road Shanghai 200233 China.

Guanlan Huang (G)

Department of Pharmaceutical Sciences Laboratory Åbo Akademi University 20520 Turku Finland.

Tuo Jin (T)

School of Pharmacy Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China.

Wenguo Cui (W)

Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 China.
State Key Laboratory of Molecular Engineering of Polymers Fudan University No. 220 Handan Road Shanghai 200433 China.

Bruno Sarmento (B)

I3S-Instituto de Investigação e Inovação em Saúde Universidade do Porto Rua Alfredo Allen, 208 Porto 4200-135 Portugal.
INEB-Instituto de Engenharia Biomédica Universidade do Porto Rua Alfredo Allen, 208 Porto 4200-135 Portugal.
CESPU-Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde Rua Central de Gandra 1317 Gandra 4585-116 Portugal.

Lianfu Deng (L)

Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 China.

Cunyi Fan (C)

Department of Orthopaedics Shanghai Jiao Tong University Affiliated Sixth People's Hospital 600 Yishan Road Shanghai 200233 China.

Classifications MeSH