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Aligned Electrospun PLLA/Graphene Microfibers with Nanotopographical Surface Modulate the Mitochondrial Responses of Vascular Smooth Muscle Cells
Author(s) -
Li Min,
Deng Wenshuai,
Zhang Jun,
Zheng Weiping,
Yu Tao,
Zhou Qihui
Publication year - 2021
Publication title -
advanced materials interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.671
H-Index - 65
ISSN - 2196-7350
DOI - 10.1002/admi.202100229
Subject(s) - materials science , nanoporous , microfiber , biophysics , mitochondrion , electrospinning , myosin , reactive oxygen species , fiber , microbiology and biotechnology , nanotechnology , biology , polymer , composite material
Although electrospun polymer fibers with unique (bio)physicochemical features have been demonstrated to regulate cellular phenotype, their specific effect on organelles has not been examined closely. Herein, this work investigates the impact of aligned electrospun poly(L‐lactic acid) (PLLA)/graphene (Gr) microfibers with the nanoporous surface on the mitochondrial responses of human aorta smooth muscle cells. Highly aligned PLLA/Gr microfibers with an average fiber diameter of ≈1.3 µm are prepared via a novel stable jet electrospinning strategy. Nanoporous topography is formed onto individual fiber surfaces using highly volatile solvent dichloromethane and suitable ambient humidity. Further, it is found that the addition of Gr in PLLA fibers significantly facilitates the formation of mitochondrial reactive oxygen species (mROS) and adenosine triphosphate (ATP) as well as mitochondrial autophagy and division by upregulating the protein expression of microtubule‐associated protein light chain 3, mitochondrial fission 1 protein, and dynamin‐related protein 1. In contrast, the introduction of the nanoporous structure greatly inhibits the generation of mROS and ATP as well as mitochondrial autophagy and division. The work thus indicates that the incorporation of nanotopography and Gr in/on the PLLA fibers can offer additional physicochemical stimuli to regulate the mitochondrial responses of cells.