-
Je něco špatně v tomto záznamu ?
The gene expression of human endothelial cells is modulated by subendothelial extracellular matrix proteins: short-term response to laminar shear stress
J. Chlupac, E. Filova, J. Havlikova, R. Matejka, T. Riedel, M. Houska, E. Brynda, E. Pamula, M. Rémy, R. Bareille, P. Fernandez, R. Daculsi, C. Bourget, L. Bacakova, L. Bordenave,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 2008-01-01 do 2018-12-31
Health & Medicine (ProQuest)
od 2008-01-01 do 2018-12-31
- MeSH
- buněčná adheze účinky léků MeSH
- časové faktory MeSH
- endoteliální buňky účinky léků metabolismus MeSH
- extracelulární matrix - proteiny farmakologie MeSH
- fluorescenční protilátková technika MeSH
- krysa rodu rattus MeSH
- lidé MeSH
- mechanický stres * MeSH
- myši MeSH
- pevnost ve smyku * MeSH
- povrchová plasmonová rezonance MeSH
- proliferace buněk účinky léků MeSH
- regulace genové exprese účinky léků MeSH
- smáčivost MeSH
- stanovení celkové genové exprese MeSH
- vena saphena cytologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Vascular surgery for atherosclerosis is confronted by the lack of a suitable bypass material. Tissue engineering strives to produce bio-artificial conduits to provide resistance to thrombosis. The objectives of our study were to culture endothelial cells (EC) on composite assemblies of extracellular matrix proteins, and to evaluate the cellular phenotype under flow. Cell-adhesive assemblies were fabricated on glass slides as combinations of collagen (Co), laminin (LM), and fibronectin (FN), resulting in three samples: Co, Co/LM, and Co/FN. Surface topography, roughness, and wettability were determined. Human saphenous vein EC were harvested from cardiac patients, cultured on the assemblies and submitted to laminar shear stress (SS) of 12 dyn/cm(2) for 40, 80, and 120 min. Cell retention was assessed and qRT-PCR of adhesion genes (VE-cadherin, vinculin, KDR, CD-31 or PECAM-1, β1-integrins) and metabolic genes (t-PA, NF-κB, eNOS and MMP-1) was performed. Quantitative immunofluorescence of VE cadherin, vinculin, KDR, and vonWillebrand factor was performed after 2 and 6 h of flow. Static samples were excluded from shearing. The cells reached confluence with similar growth curves. The cells on Co/LM and Co/FN were resistant to flow up to 120 min but minor desquamation occurred on Co corresponding with temporary downregulation of VE cadherin and vinculin-mRNA and decreased fluorescence of vinculin. The cells seeded on Co/LM initially more upregulated vinculin-mRNA and also the inflammatory factor NF-κB, and the cells plated on Co/FN changed the expression profile minimally in comparison with the static control. Fluorescence of VE cadherin and vonWillebrand factor was enhanced on Co/FN. The cells cultured on Co/LM and Co/FN increased the vinculin fluorescence and expressed more VE cadherin and KDR-mRNA than the cells on Co. The cells plated on Co/FN upregulated the mRNA of VE cadherin, CD-31, and MMP 1 to a greater extent than the cells on Co/LM and they enhanced the fluorescence of VE cadherin, KDR, and vonWillebrand factor. Some of these changes sustained up to 6 h of flow, as confirmed by immunofluorescence. Combined matrices Co/LM and Co/FN seem to be more suitable for EC seeding and retention under flow. Moreover, Co/FN matrix promoted slightly more favorable cellular phenotype than Co/LM under SS of 2-6 h.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15023547
- 003
- CZ-PrNML
- 005
- 20150723104019.0
- 007
- ta
- 008
- 150709s2014 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1089/ten.TEA.2013.0153 $2 doi
- 035 __
- $a (PubMed)24606163
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Chlupac, Jaroslav $u 1 Department of Biomaterials and Tissue Engineering, Institute of Physiology, Academy of Sciences of the Czech Republic , Prague, Czech Republic .
- 245 14
- $a The gene expression of human endothelial cells is modulated by subendothelial extracellular matrix proteins: short-term response to laminar shear stress / $c J. Chlupac, E. Filova, J. Havlikova, R. Matejka, T. Riedel, M. Houska, E. Brynda, E. Pamula, M. Rémy, R. Bareille, P. Fernandez, R. Daculsi, C. Bourget, L. Bacakova, L. Bordenave,
- 520 9_
- $a Vascular surgery for atherosclerosis is confronted by the lack of a suitable bypass material. Tissue engineering strives to produce bio-artificial conduits to provide resistance to thrombosis. The objectives of our study were to culture endothelial cells (EC) on composite assemblies of extracellular matrix proteins, and to evaluate the cellular phenotype under flow. Cell-adhesive assemblies were fabricated on glass slides as combinations of collagen (Co), laminin (LM), and fibronectin (FN), resulting in three samples: Co, Co/LM, and Co/FN. Surface topography, roughness, and wettability were determined. Human saphenous vein EC were harvested from cardiac patients, cultured on the assemblies and submitted to laminar shear stress (SS) of 12 dyn/cm(2) for 40, 80, and 120 min. Cell retention was assessed and qRT-PCR of adhesion genes (VE-cadherin, vinculin, KDR, CD-31 or PECAM-1, β1-integrins) and metabolic genes (t-PA, NF-κB, eNOS and MMP-1) was performed. Quantitative immunofluorescence of VE cadherin, vinculin, KDR, and vonWillebrand factor was performed after 2 and 6 h of flow. Static samples were excluded from shearing. The cells reached confluence with similar growth curves. The cells on Co/LM and Co/FN were resistant to flow up to 120 min but minor desquamation occurred on Co corresponding with temporary downregulation of VE cadherin and vinculin-mRNA and decreased fluorescence of vinculin. The cells seeded on Co/LM initially more upregulated vinculin-mRNA and also the inflammatory factor NF-κB, and the cells plated on Co/FN changed the expression profile minimally in comparison with the static control. Fluorescence of VE cadherin and vonWillebrand factor was enhanced on Co/FN. The cells cultured on Co/LM and Co/FN increased the vinculin fluorescence and expressed more VE cadherin and KDR-mRNA than the cells on Co. The cells plated on Co/FN upregulated the mRNA of VE cadherin, CD-31, and MMP 1 to a greater extent than the cells on Co/LM and they enhanced the fluorescence of VE cadherin, KDR, and vonWillebrand factor. Some of these changes sustained up to 6 h of flow, as confirmed by immunofluorescence. Combined matrices Co/LM and Co/FN seem to be more suitable for EC seeding and retention under flow. Moreover, Co/FN matrix promoted slightly more favorable cellular phenotype than Co/LM under SS of 2-6 h.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčná adheze $x účinky léků $7 D002448
- 650 _2
- $a proliferace buněk $x účinky léků $7 D049109
- 650 _2
- $a endoteliální buňky $x účinky léků $x metabolismus $7 D042783
- 650 _2
- $a extracelulární matrix - proteiny $x farmakologie $7 D016326
- 650 _2
- $a fluorescenční protilátková technika $7 D005455
- 650 _2
- $a stanovení celkové genové exprese $7 D020869
- 650 _2
- $a regulace genové exprese $x účinky léků $7 D005786
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a vena saphena $x cytologie $7 D012501
- 650 12
- $a pevnost ve smyku $7 D033081
- 650 12
- $a mechanický stres $7 D013314
- 650 _2
- $a povrchová plasmonová rezonance $7 D020349
- 650 _2
- $a časové faktory $7 D013997
- 650 _2
- $a smáčivost $7 D017155
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Filova, Elena
- 700 1_
- $a Havlikova, Jana
- 700 1_
- $a Matejka, Roman
- 700 1_
- $a Riedel, Tomas
- 700 1_
- $a Houska, Milan
- 700 1_
- $a Brynda, Eduard
- 700 1_
- $a Pamula, Elzbieta
- 700 1_
- $a Rémy, Murielle
- 700 1_
- $a Bareille, Reine
- 700 1_
- $a Fernandez, Philippe
- 700 1_
- $a Daculsi, Richard
- 700 1_
- $a Bourget, Chantal
- 700 1_
- $a Bacakova, Lucie
- 700 1_
- $a Bordenave, Laurence
- 773 0_
- $w MED00163782 $t Tissue engineering. Part A $x 1937-335X $g Roč. 20, č. 15-16 (2014), s. 2253-64
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24606163 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150709 $b ABA008
- 991 __
- $a 20150723104057 $b ABA008
- 999 __
- $a ok $b bmc $g 1083884 $s 906540
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 20 $c 15-16 $d 2253-64 $i 1937-335X $m Tissue engineering. Part A $n Tissue Eng Part A $x MED00163782
- LZP __
- $a Pubmed-20150709