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Rapid Extracellular Matrix Remodeling via Gene‐Electrospun Fibers as a “Patch” for Tissue Regeneration
Author(s) -
Jin Jing,
Saiding Qimanguli,
Wang Xianjing,
Qin Menglu,
Xiang Yi,
Cheng Ruoyu,
Cui Wenguo,
Chen Xinliang
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202009879
Subject(s) - extracellular matrix , elastin , lysyl oxidase , regeneration (biology) , materials science , gene delivery , microbiology and biotechnology , biomedical engineering , electrospinning , transfection , biophysics , nanotechnology , gene , chemistry , biology , polymer , biochemistry , medicine , pathology , composite material
A break of extracellular matrix (ECM) balance can cause several degenerative changes in soft tissues. To reverse the imbalance fundamentally, a recently developed treatment, gene therapy, came to attention. However, the efficiency of the approach is limited because long‐term localized presence and bioactivity are difficult to achieve. Here, reconstituted lysyl oxidase‐like 1 (LOXL1) plasmids (pLOXL1) are loaded into nanoliposomes by a microfluidic chip, followed by encapsulation into the core layer of core–shell nanofibers by microsol‐electrospinning to achieve local accumulation and biological availability of the constructs and enable rapid ECM response. Results show that the pLOXL1‐Lipo@PLCL‐HA achieves the sustained release of pLOXL1 over a 30‐day period, with its transfection efficiency maintained above 50%. In a rabbit model of abdominal hernia, the long‐term collagen remodeling density is raised by over 90% in the pLOXL1‐Lipo@PLCL‐HA implanted animals compared to the control animals. The expression levels of ECM gene (COL1A1, COL3A1, Elastin, Fubilin5) are significantly increased. Collectively, this study establishes that pLOXL1‐Lipo@PLCL‐HA accelerates local ECM reconstruction via effective and reliable gene delivery as a potential base material of a “patch” for pelvic floor repairment, and identifies the key principles for design of LOXL1‐incorporated scaffolds for ECM regeneration.