-
Something wrong with this record ?
The role of smooth muscle cells in vessel wall pathophysiology and reconstruction using bioactive synthetic polymers
M. Pařízek, K. Novotná, L. Bačáková
Language English Country Czech Republic
Document type Review
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Cell Differentiation MeSH
- Blood Vessel Prosthesis MeSH
- Endothelial Cells physiology pathology MeSH
- Extracellular Matrix metabolism MeSH
- Stem Cells metabolism pathology MeSH
- Humans MeSH
- Myocytes, Smooth Muscle physiology pathology MeSH
- Vascular Diseases pathology therapy MeSH
- Polymers chemistry MeSH
- Cell Proliferation MeSH
- Muscle, Smooth, Vascular pathology MeSH
- Tissue Scaffolds MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Review MeSH
This review summarizes recent trends in the construction of bioartificial vascular replacements, i.e. hybrid grafts containing synthetic polymeric scaffolds and cells. In these advanced replacements, vascular smooth muscle cells (VSMC) should be considered as a physiological component, although it is known that activation of the migration and proliferation of VSMC plays an important role in the onset and development of vascular diseases, and also in restenosis of currently used vascular grafts. Therefore, in novel bioartificial vascular grafts, VSMCs should be kept in quiescent mature contractile phenotype. This can be achieved by (1) appropriate physical and chemical properties of the material, such as its chemical composition, polarity, wettability, surface roughness and topography, electrical charge and conductivity, functionalization with biomolecules and mechanical properties, (2) appropriate cell culture conditions, such as composition of cell culture media and dynamic load, namely cyclic strain, and (3) the presence of a confluent, mature, semipermeable, non-thrombogenic and non-immunogenic endothelial cell (EC) barrier, covering the luminal surface of the graft and separating the VSMCs from the blood. Both VSMCs and ECs can also be differentiated from stem and progenitor cells of various sources. In the case of degradable scaffolds, the material will gradually be removed by the cells and will be replaced by their own new extracellular matrix. Thus, the material component in advanced blood vessel substitutes acts as a temporary scaffold that promotes regeneration of the damaged vascular tissue.
References provided by Crossref.org
Lit.: 86
- 000
- 00000naa 2200000 a 4500
- 001
- bmc11032011
- 003
- CZ-PrNML
- 005
- 20130131145917.0
- 008
- 110912s2011 xr e eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.932038 $2 doi
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Pařízek, Martin $7 xx0137109
- 245 14
- $a The role of smooth muscle cells in vessel wall pathophysiology and reconstruction using bioactive synthetic polymers / $c M. Pařízek, K. Novotná, L. Bačáková
- 314 __
- $a Department of Growth and Differentiation of Cell Populations, Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic. lucy@biomed.cas.cz.
- 504 __
- $a Lit.: 86
- 520 9_
- $a This review summarizes recent trends in the construction of bioartificial vascular replacements, i.e. hybrid grafts containing synthetic polymeric scaffolds and cells. In these advanced replacements, vascular smooth muscle cells (VSMC) should be considered as a physiological component, although it is known that activation of the migration and proliferation of VSMC plays an important role in the onset and development of vascular diseases, and also in restenosis of currently used vascular grafts. Therefore, in novel bioartificial vascular grafts, VSMCs should be kept in quiescent mature contractile phenotype. This can be achieved by (1) appropriate physical and chemical properties of the material, such as its chemical composition, polarity, wettability, surface roughness and topography, electrical charge and conductivity, functionalization with biomolecules and mechanical properties, (2) appropriate cell culture conditions, such as composition of cell culture media and dynamic load, namely cyclic strain, and (3) the presence of a confluent, mature, semipermeable, non-thrombogenic and non-immunogenic endothelial cell (EC) barrier, covering the luminal surface of the graft and separating the VSMCs from the blood. Both VSMCs and ECs can also be differentiated from stem and progenitor cells of various sources. In the case of degradable scaffolds, the material will gradually be removed by the cells and will be replaced by their own new extracellular matrix. Thus, the material component in advanced blood vessel substitutes acts as a temporary scaffold that promotes regeneration of the damaged vascular tissue.
- 650 02
- $a zvířata $7 D000818
- 650 02
- $a cévní protézy $7 D001807
- 650 02
- $a buněčná diferenciace $7 D002454
- 650 02
- $a proliferace buněk $7 D049109
- 650 02
- $a endoteliální buňky $x fyziologie $x patologie $7 D042783
- 650 02
- $a extracelulární matrix $x metabolismus $7 D005109
- 650 02
- $a lidé $7 D006801
- 650 02
- $a svaly hladké cévní $x patologie $7 D009131
- 650 02
- $a myocyty hladké svaloviny $x fyziologie $x patologie $7 D032389
- 650 02
- $a polymery $x chemie $7 D011108
- 650 02
- $a kmenové buňky $x metabolismus $x patologie $7 D013234
- 650 02
- $a tkáňové podpůrné struktury $7 D054457
- 650 02
- $a nemoci cév $x patologie $x terapie $7 D014652
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Novotná, Kamila $7 xx0128988
- 700 1_
- $a Bačáková, Lucie, $d 1958- $7 xx0070525
- 773 0_
- $w MED00003824 $t Physiological research $g Roč. 60, č. 3 (2011), s. 419-437 $x 0862-8408
- 856 41
- $u http://www.biomed.cas.cz/physiolres/pdf/60/60_419.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 2
- 990 __
- $a 20110912095705 $b ABA008
- 991 __
- $a 20130131150044 $b ABA008
- 999 __
- $a ok $b bmc $g 877091 $s 742087
- BAS __
- $a 3
- BMC __
- $a 2011 $b 60 $c 3 $d 419-437 $m Physiological research $x MED00003824
- LZP __
- $a 2011-16/mkme