scholarly journals Effect of hydrogel coating of smooth muscle cells orientated on a biomaterial surface: A protective outer layer for a cellularized vascular prosthesis with surface guidance.

Author(s):  
Irvine Scott ◽  
Zhao Xinxin ◽  
Agrawal Animesh ◽  
Cao Ye ◽  
Lim Pei Qi ◽  
...  
ASAIO Journal ◽  
1993 ◽  
Vol 39 (3) ◽  
pp. M746-M749 ◽  
Author(s):  
YASUHARU NOISHIKI ◽  
YOSHIHISA YAMANE ◽  
YASUKO TOMIZAWA ◽  
TAKAFUMI OKOSHI ◽  
SLNICHI SATOH ◽  
...  

ASAIO Journal ◽  
1993 ◽  
Vol 39 (3) ◽  
pp. M746-M749 ◽  
Author(s):  
Yasuharu Noishiki ◽  
Yoshihisa Yamane ◽  
Yasuko Tomizawa ◽  
Takafumi Okoshi ◽  
Sinichi Satoh ◽  
...  

RSC Advances ◽  
2021 ◽  
Vol 11 (50) ◽  
pp. 31783-31790
Author(s):  
Mei-Xi Li ◽  
Lei Li ◽  
Si-Yuan Zhou ◽  
Jian-Hua Cao ◽  
Wei-Hua Liang ◽  
...  

To mimic blood vessels, a polycaprolactone tubular scaffold was prepared via electrospinning and winding. Endothelial cells were cultured on the inner layer with axial nanofibers and smooth muscle cells were cultured on the outer layer with circumferential nanofibers.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yin Chen ◽  
Peng Gao ◽  
Lu Huang ◽  
Xing Tan ◽  
Ningling Zhou ◽  
...  

AbstractVascular stent is viewed as one of the greatest advancements in interventional cardiology. However, current approved stents suffer from in-stent restenosis associated with neointimal hyperplasia or stent thrombosis. Herein, we develop a nitric oxide-eluting (NOE) hydrogel coating for vascular stents inspired by the biological functions of nitric oxide for cardiovascular system. Our NOE hydrogel is mechanically tough and could selectively facilitate the adhesion of endothelial cells. Besides, it is non-thrombotic and capable of inhibiting smooth muscle cells. Transcriptome analysis unravels the NOE hydrogel could modulate the inflammatory response and induce the relaxation of smooth muscle cells. In vivo study further demonstrates vascular stents coated with it promote rapid restoration of native endothelium, and persistently suppress inflammation and neointimal hyperplasia in both leporine and swine models. We expect such NOE hydrogel will open an avenue to the surface engineering of vascular implants for better clinical outcomes.


1985 ◽  
Vol 55 ◽  
Author(s):  
Ch. R. H. Wildevuur ◽  
B. van der Lei

ABSTRACTThe biological repair process tends to cover a vascular prosthesis by normal arterial wall tissue. This process was successfully utilized in rats to form eventually a neo-artery induced by a temporary physiologically functioning prosthetic scaffold. Essential for the regeneration of a normal compliant neo-artery was the initial physiological campliance and the gradual degradation of the prosthetic grafts. Only then the regenerating neo-media was effectively stimulated by the pulsatile flow to produce elastic laminae. Regeneration of the arterial wall could be enhanced by seeding smooth muscle cells. The same concept was successfully applied to replace the trachea and oesophagus in rabbits. These results demonstrate that regeneration of biological organs can be induced by temporary acting artificial organs, which are anatomically correct and superior to permanently implanted artificially organs.


Author(s):  
J.M. Minda ◽  
E. Dessy ◽  
G. G. Pietra

Pulmonary lymphangiomyomatosis (PLAM) is a rare disease occurring exclusively in women of reproductive age. It involves the lungs, lymph nodes and lymphatic ducts. In the lungs, it is characterized by the proliferation of smooth muscle cells around lymphatics in the bronchovascular bundles, lobular septa and pleura The nature of smooth muscle proliferation in PLAM is still unclear. Recently, reactivity of the smooth muscle cells for HMB-45, a melanoma-related antigen has been reported by immunohistochemistry. The purpose of this study was the ultrastructural localization of HMB-45 immunoreactivity in these cells using gold-labeled antibodies.Lung tissue from three cases of PLAM, referred to our Institution for lung transplantation, was embedded in either Poly/Bed 812 post-fixed in 1% osmium tetroxide, or in LR White, without osmication. For the immunogold technique, thin sections were placed on Nickel grids and incubated with affinity purified, monoclonal anti-melanoma antibody HMB-45 (1:1) (Enzo Diag. Co) overnight at 4°C. After extensive washing with PBS, grids were treated with Goat-anti-mouse-IgG-Gold (5nm) (1:10) (Amersham Life Sci) for 1 hour, at room temperature.


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