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Comparative gene expression profiling of human primary endotheliocytes cultivated on polyurethane-based electrospun 3D matrices and natural decellularized vein. / Chernonosova, Vera S.; Laktionov, Petr P.; Murashov, Ivan S. и др.

в: Biomedical Materials (Bristol), Том 15, № 4, 045012, 07.2020.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Chernonosova VS, Laktionov PP, Murashov IS, Karpenko AA, Laktionov PP. Comparative gene expression profiling of human primary endotheliocytes cultivated on polyurethane-based electrospun 3D matrices and natural decellularized vein. Biomedical Materials (Bristol). 2020 июль;15(4):045012. doi: 10.1088/1748-605X/ab7d84

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BibTeX

@article{c59e082a076a44b5a026a9a6ba7fb2d0,
title = "Comparative gene expression profiling of human primary endotheliocytes cultivated on polyurethane-based electrospun 3D matrices and natural decellularized vein",
abstract = "The formation of a continuous layer of normally functioning endothelium on the lumen surface of small diameter vascular grafts is considered a prerequisite of their long-term functioning without stenosis. Thus, materials supporting not only endothelialization but also the normal functioning state of endotheliocytes are demanded. In this study, we have evaluated the functional state of human umbilical vein endothelial cells (HUVEC) cultivated on the surface of autologous decellularized human umbilical vein and electrospun polyurethane-based matrices by next generation sequencing gene expression profiling. Three types of matrices produced by electrospinning from hexafluoroisopropanol solutions of pure TECOFLEX{\texttrademark} EG-80A polyurethane, polyurethane with gelatin and polyurethane with gelatin and bivalirudin were studied. Cells cultivated on different supports were subjected to RNA-Seq profiling on an Illumina HiSeq platform. The data demonstrated that the structure of 3D matrices and the chemical composition of the fibers have a significant effect on the gene expression profiles of HUVEC. The results suggest that protein-enriched polyurethane-based 3D matrices represent a convenient surface for obtaining a normally functioning endothelial layer. ",
keywords = "decellularized vein, electrospun 3D matrices, endothelialization, gene expression, polyurethane TECOFLEX EG-80A, CELLS, LOCALIZATION, ACTIVATION, CHOLESTEROL, UBIQUITINATION, OVEREXPRESSION, EVOLUTION, IN-SITU ENDOTHELIALIZATION, DEGRADATION, SCAFFOLD",
author = "Chernonosova, {Vera S.} and Laktionov, {Petr P.} and Murashov, {Ivan S.} and Karpenko, {Andrey A.} and Laktionov, {Pavel P.}",
year = "2020",
month = jul,
doi = "10.1088/1748-605X/ab7d84",
language = "English",
volume = "15",
journal = "Biomedical Materials (Bristol)",
issn = "1748-6041",
publisher = "IOP Publishing Ltd.",
number = "4",

}

RIS

TY - JOUR

T1 - Comparative gene expression profiling of human primary endotheliocytes cultivated on polyurethane-based electrospun 3D matrices and natural decellularized vein

AU - Chernonosova, Vera S.

AU - Laktionov, Petr P.

AU - Murashov, Ivan S.

AU - Karpenko, Andrey A.

AU - Laktionov, Pavel P.

PY - 2020/7

Y1 - 2020/7

N2 - The formation of a continuous layer of normally functioning endothelium on the lumen surface of small diameter vascular grafts is considered a prerequisite of their long-term functioning without stenosis. Thus, materials supporting not only endothelialization but also the normal functioning state of endotheliocytes are demanded. In this study, we have evaluated the functional state of human umbilical vein endothelial cells (HUVEC) cultivated on the surface of autologous decellularized human umbilical vein and electrospun polyurethane-based matrices by next generation sequencing gene expression profiling. Three types of matrices produced by electrospinning from hexafluoroisopropanol solutions of pure TECOFLEX™ EG-80A polyurethane, polyurethane with gelatin and polyurethane with gelatin and bivalirudin were studied. Cells cultivated on different supports were subjected to RNA-Seq profiling on an Illumina HiSeq platform. The data demonstrated that the structure of 3D matrices and the chemical composition of the fibers have a significant effect on the gene expression profiles of HUVEC. The results suggest that protein-enriched polyurethane-based 3D matrices represent a convenient surface for obtaining a normally functioning endothelial layer.

AB - The formation of a continuous layer of normally functioning endothelium on the lumen surface of small diameter vascular grafts is considered a prerequisite of their long-term functioning without stenosis. Thus, materials supporting not only endothelialization but also the normal functioning state of endotheliocytes are demanded. In this study, we have evaluated the functional state of human umbilical vein endothelial cells (HUVEC) cultivated on the surface of autologous decellularized human umbilical vein and electrospun polyurethane-based matrices by next generation sequencing gene expression profiling. Three types of matrices produced by electrospinning from hexafluoroisopropanol solutions of pure TECOFLEX™ EG-80A polyurethane, polyurethane with gelatin and polyurethane with gelatin and bivalirudin were studied. Cells cultivated on different supports were subjected to RNA-Seq profiling on an Illumina HiSeq platform. The data demonstrated that the structure of 3D matrices and the chemical composition of the fibers have a significant effect on the gene expression profiles of HUVEC. The results suggest that protein-enriched polyurethane-based 3D matrices represent a convenient surface for obtaining a normally functioning endothelial layer.

KW - decellularized vein

KW - electrospun 3D matrices

KW - endothelialization

KW - gene expression

KW - polyurethane TECOFLEX EG-80A

KW - CELLS

KW - LOCALIZATION

KW - ACTIVATION

KW - CHOLESTEROL

KW - UBIQUITINATION

KW - OVEREXPRESSION

KW - EVOLUTION

KW - IN-SITU ENDOTHELIALIZATION

KW - DEGRADATION

KW - SCAFFOLD

UR - http://www.scopus.com/inward/record.url?scp=85085960431&partnerID=8YFLogxK

U2 - 10.1088/1748-605X/ab7d84

DO - 10.1088/1748-605X/ab7d84

M3 - Article

C2 - 32143210

AN - SCOPUS:85085960431

VL - 15

JO - Biomedical Materials (Bristol)

JF - Biomedical Materials (Bristol)

SN - 1748-6041

IS - 4

M1 - 045012

ER -

ID: 24616254