RGD peptide-displaying M13 bacteriophage/PLGA nanofibers as cell-adhesive matrices for smooth muscle cells

被引:10
|
作者
Shin, Yong Cheol [1 ]
Lee, Jong Ho [1 ]
Jin, Oh Seong [1 ]
Lee, Eun Ji [1 ]
Jin, Lin Hua [1 ]
Kim, Chang-Seok [1 ]
Hong, Suck Won [1 ]
Han, Dong-Wook [1 ]
Kim, Chuntae [2 ]
Oh, Jin-Woo [2 ]
机构
[1] Pusan Natl Univ, Dept Cognomechtron Engn, Pusan 609735, South Korea
[2] Pusan Natl Univ, Dept Nanomat Engn, Coll Nanosci & Nanotechnol, Pusan 609735, South Korea
关键词
M13; bacteriophage; PLGA; Electrospinning; RGD peptide; Extracellular matrix; EXTRACELLULAR-MATRIX; PHAGE; DIFFERENTIATION; DELIVERY;
D O I
10.3938/jkps.66.12
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Extracellular matrices (ECMs) are network structures that play an essential role in regulating cellular growth and differentiation. In this study, novel nanofibrous matrices were fabricated by electrospinning M13 bacteriophage and poly(lactic-co-glycolic acid) (PLGA) and were shown to be structurally and functionally similar to natural ECMs. A genetically-engineered M13 bacteriophage was constructed to display Arg-Gly-Asp (RGD) peptides on its surface. The physicochemical properties of RGD peptide-displaying M13 bacteriophage (RGD-M13 phage)/PLGA nanofibers were characterized by using scanning electron microscopy and Fourier-transform infrared spectroscopy. We used immunofluorescence staining to confirm that M13 bacteriophages were homogenously distributed in RGD-M13 phage/PLGA matrices. Furthermore, RGD-M13 phage/PLGA nanofibrous matrices, having excellent biocompatibility, can enhance the behaviors of vascular smooth muscle cells. This result suggests that RGD-M13 phage/PLGA nanofibrous matrices have potentials to serve as tissue engineering scaffolds.
引用
收藏
页码:12 / 16
页数:5
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