-
Je něco špatně v tomto záznamu ?
Cell adhesion and growth enabled by biomimetic oligopeptide modification of a polydopamine-poly(ethylene oxide) protein repulsive surface
J. Musilkova, I. Kotelnikov, K. Novotna, O. Pop-Georgievski, F. Rypacek, L. Bacakova, V. Proks,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2007-11-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
ROAD: Directory of Open Access Scholarly Resources
od 2002
- MeSH
- adsorpce MeSH
- biomimetika * MeSH
- buněčná adheze * MeSH
- exprese genu MeSH
- fibronektiny chemie genetika MeSH
- indoly chemie MeSH
- kultivované buňky MeSH
- lidé MeSH
- molekulární sekvence - údaje MeSH
- oligopeptidy chemie MeSH
- polyethylenglykoly chemie MeSH
- polymery chemie MeSH
- povrchové vlastnosti MeSH
- sekvence aminokyselin MeSH
- talin genetika MeSH
- vinkulin genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Protein-repulsive surfaces modified with ligands for cell adhesion receptors have been widely developed for controlling the cell adhesion and growth in tissue engineering. However, the question of matrix production and deposition by cells on these surfaces has rarely been addressed. In this study, protein-repulsive polydopamine-poly(ethylene oxide) (PDA-PEO) surfaces were functionalized with an RGD-containing peptide (RGD), with a collagen-derived peptide binding fibronectin (Col), or by a combination of these peptides (RGD + Col, ratio 1:1) in concentrations of 90 fmol/cm(2) and 700 fmol/cm(2) for each peptide type. When seeded with vascular endothelial CPAE cells, the PDA-PEO surfaces proved to be completely non-adhesive for cells. On surfaces with lower peptide concentrations and from days 1 to 3 after seeding, cell adhesion and growth was restored practically only on the RGD-modified surface. However, from days 3 to 7, cell adhesion and growth was improved on surfaces modified with Col and with RGD + Col. At higher peptide concentrations, the cell adhesion and growth was markedly improved on all peptide-modified surfaces in both culture intervals. However, the collagen-derived peptide did not increase the expression of fibronectin in the cells. The deposition of fibronectin on the material surface was generally very low and similar on all peptide-modified surfaces. Nevertheless, the RGD + Col surfaces exhibited the highest cell adhesion stability under a dynamic load, which correlated with the highest expression of talin and vinculin in the cells on these surfaces. A combination of RGD + Col therefore seems to be the most promising for surface modification of biomaterials, e.g. vascular prostheses.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16028124
- 003
- CZ-PrNML
- 005
- 20161025104304.0
- 007
- ta
- 008
- 161005s2015 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s10856-015-5583-3 $2 doi
- 024 7_
- $a 10.1007/s10856-015-5583-3 $2 doi
- 035 __
- $a (PubMed)26449443
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Musilkova, Jana $u Department of Biomaterials and Tissue Engineering, Institute of Physiology of the Czech Academy of Sciences, v.v.i., Videnska 1083, 14220, Prague 4 - Krc, Czech Republic.
- 245 10
- $a Cell adhesion and growth enabled by biomimetic oligopeptide modification of a polydopamine-poly(ethylene oxide) protein repulsive surface / $c J. Musilkova, I. Kotelnikov, K. Novotna, O. Pop-Georgievski, F. Rypacek, L. Bacakova, V. Proks,
- 520 9_
- $a Protein-repulsive surfaces modified with ligands for cell adhesion receptors have been widely developed for controlling the cell adhesion and growth in tissue engineering. However, the question of matrix production and deposition by cells on these surfaces has rarely been addressed. In this study, protein-repulsive polydopamine-poly(ethylene oxide) (PDA-PEO) surfaces were functionalized with an RGD-containing peptide (RGD), with a collagen-derived peptide binding fibronectin (Col), or by a combination of these peptides (RGD + Col, ratio 1:1) in concentrations of 90 fmol/cm(2) and 700 fmol/cm(2) for each peptide type. When seeded with vascular endothelial CPAE cells, the PDA-PEO surfaces proved to be completely non-adhesive for cells. On surfaces with lower peptide concentrations and from days 1 to 3 after seeding, cell adhesion and growth was restored practically only on the RGD-modified surface. However, from days 3 to 7, cell adhesion and growth was improved on surfaces modified with Col and with RGD + Col. At higher peptide concentrations, the cell adhesion and growth was markedly improved on all peptide-modified surfaces in both culture intervals. However, the collagen-derived peptide did not increase the expression of fibronectin in the cells. The deposition of fibronectin on the material surface was generally very low and similar on all peptide-modified surfaces. Nevertheless, the RGD + Col surfaces exhibited the highest cell adhesion stability under a dynamic load, which correlated with the highest expression of talin and vinculin in the cells on these surfaces. A combination of RGD + Col therefore seems to be the most promising for surface modification of biomaterials, e.g. vascular prostheses.
- 650 _2
- $a adsorpce $7 D000327
- 650 _2
- $a sekvence aminokyselin $7 D000595
- 650 12
- $a biomimetika $7 D032701
- 650 12
- $a buněčná adheze $7 D002448
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a fibronektiny $x chemie $x genetika $7 D005353
- 650 _2
- $a exprese genu $7 D015870
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a indoly $x chemie $7 D007211
- 650 _2
- $a molekulární sekvence - údaje $7 D008969
- 650 _2
- $a oligopeptidy $x chemie $7 D009842
- 650 _2
- $a polyethylenglykoly $x chemie $7 D011092
- 650 _2
- $a polymery $x chemie $7 D011108
- 650 _2
- $a povrchové vlastnosti $7 D013499
- 650 _2
- $a talin $x genetika $7 D016608
- 650 _2
- $a vinkulin $x genetika $7 D016596
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kotelnikov, Ilya $u Department of Biomaterials and Bioanalogous Systems, Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, v.v.i., Heyrovsky Sq. 1888/2, 16206, Prague 6, Czech Republic.
- 700 1_
- $a Novotna, Katarina $u Department of Biomaterials and Tissue Engineering, Institute of Physiology of the Czech Academy of Sciences, v.v.i., Videnska 1083, 14220, Prague 4 - Krc, Czech Republic.
- 700 1_
- $a Pop-Georgievski, Ognen $u Department of Chemistry and Physics of Surfaces and Biointerfaces, Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, v.v.i., Heyrovsky Sq. 1888/2, 16206, Prague 6, Czech Republic.
- 700 1_
- $a Rypacek, Frantisek $u Department of Biomaterials and Bioanalogous Systems, Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, v.v.i., Heyrovsky Sq. 1888/2, 16206, Prague 6, Czech Republic.
- 700 1_
- $a Bacakova, Lucie $u Department of Biomaterials and Tissue Engineering, Institute of Physiology of the Czech Academy of Sciences, v.v.i., Videnska 1083, 14220, Prague 4 - Krc, Czech Republic. lucy@biomed.cas.cz.
- 700 1_
- $a Proks, Vladimir $u Department of Biomaterials and Bioanalogous Systems, Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, v.v.i., Heyrovsky Sq. 1888/2, 16206, Prague 6, Czech Republic. proks@imc.cas.cz.
- 773 0_
- $w MED00002780 $t Journal of materials science. Materials in medicine $x 1573-4838 $g Roč. 26, č. 11 (2015), s. 253
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26449443 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20161005 $b ABA008
- 991 __
- $a 20161025104718 $b ABA008
- 999 __
- $a ok $b bmc $g 1166438 $s 952754
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 26 $c 11 $d 253 $e 20151008 $i 1573-4838 $m Journal of materials science. Materials in medicine $n J Mater Sci Mater Med $x MED00002780
- LZP __
- $a Pubmed-20161005