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L773:1557 1939 OR L773:1557 1947
 

Search: L773:1557 1939 OR L773:1557 1947 > Production of extra...

Production of extracellular matrix components in tissue-engineered blood vessels

Heydarkhan-Hagvall, Sepideh, 1969 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Esguerra, Maricris, 1981 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Helenius, Gisela, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
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Söderberg, Rigmor, 1943 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Johansson, Bengt R, 1947 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
Risberg, Bo, 1941 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
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 (creator_code:org_t)
Mary Ann Liebert Inc, 2006
2006
English.
In: Tissue engineering. - : Mary Ann Liebert Inc. - 1076-3279 .- 1557-8690. ; 12:4, s. 831-42
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Morphology and compliance of tissue-engineered blood vessels (TEBV) are dependent on the culture period and production of extracellular matrix (ECM) components in order to increase the strength of the developing tissue. The aim of the present study was to evaluate the potential of TEBVs to produce an ECM similar to native arteries and veins. Human smooth muscle cells (SMC) were seeded onto the poly(glycolic acid) (PGA) scaffold and placed in bioreactors filled with DMEM supplemented with growth factors. After 6 weeks, the vessels were harvested from the bioreactors and seeded with human endothelial cells at the lumen for another 3 days. Then, the TEBVs were harvested for RNA and protein isolation for further RT-PCR and Western blot. TEBVs had a similar macroscopic appearance to that of native vessels with no visible evidence of the original PGA. Histological and immunohistochemical analyses indicated the presence of high cell density and development of a highly organized structure of ECM. After 6 weeks of culture, there were significantly lower gene expression of SMC-specific markers, such as alpha-actin, caldesmon, and vimentin, and proteoglycans, such as biglycan, decorin, and versican, and other ECM components, such as collagen I and elastin, in TEBVs, with and without pulsatile conditions, compared to that of native arteries. Gene expression of fibronectin was significantly lower in TEBVs grown during pulsatile conditions compared to that of native arteries. No difference was observed in TEBVs grown during non-pulsatile conditions. The presence of alpha-actin, collagen I, decorin, and fibronectin at protein level was demonstrated in TEBVs with and without pulsatile conditions after 6 weeks and in native veins and arteries as well. How this deviation translates into mechanical properties remains to be explored.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Keyword

Bioreactors
Blood Vessels/cytology/drug effects/*physiology/ultrastructure
Cells
Cultured
Culture Media/chemistry
Endothelial Cells/cytology/drug effects/*physiology/ultrastructure
Endothelium
Vascular/cytology
Extracellular Matrix/chemistry/*metabolism
Growth Substances/pharmacology
Humans
Mesenteric Artery
Superior/surgery
Muscle
Smooth
Vascular/cytology/drug effects/*physiology/ultrastructure
Polyglycolic Acid/chemistry
Proteins/genetics/isolation & purification/metabolism
Saphenous Vein/cytology
Splenic Artery/surgery
Tissue Engineering/*methods

Publication and Content Type

ref (subject category)
art (subject category)

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