GARLÍKOVÁ, Zuzana, Jana DUMKOVÁ, Milan EŠNER, Anas RABATA, Zuzana KOLEDOVÁ and Aleš HAMPL. NANOSTRUCTURE AND BIOACTIVITY OF MOUSE LUNG EXTRACELLULAR MATRIX SCAFFOLDS. In 9TH INTERNATIONAL CONFERENCE ON NANOMATERIALS - RESEARCH & APPLICATION (NANOCON 2017). SLEZSKA: TANGER LTD, 2018, p. 560-566. ISBN 978-80-87294-81-9.
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Basic information
Original name NANOSTRUCTURE AND BIOACTIVITY OF MOUSE LUNG EXTRACELLULAR MATRIX SCAFFOLDS
Authors GARLÍKOVÁ, Zuzana (203 Czech Republic, guarantor, belonging to the institution), Jana DUMKOVÁ (203 Czech Republic, belonging to the institution), Milan EŠNER (203 Czech Republic, belonging to the institution), Anas RABATA (760 Syrian Arab Republic, belonging to the institution), Zuzana KOLEDOVÁ (703 Slovakia, belonging to the institution) and Aleš HAMPL (203 Czech Republic, belonging to the institution).
Edition SLEZSKA, 9TH INTERNATIONAL CONFERENCE ON NANOMATERIALS - RESEARCH & APPLICATION (NANOCON 2017), p. 560-566, 7 pp. 2018.
Publisher TANGER LTD
Other information
Original language English
Type of outcome Proceedings paper
Field of Study 21002 Nano-processes ;
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
Publication form storage medium (CD, DVD, flash disk)
RIV identification code RIV/00216224:14110/18:00100758
Organization unit Faculty of Medicine
ISBN 978-80-87294-81-9
UT WoS 000452823300092
Keywords in English Lung; extracellular matrix; nanostructure; bioactivity
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 1/3/2019 10:47.
Abstract
Extracellular matrix (ECM) forms an essential part of tissue microenvironment. Compositional and structural properties of ECM modulate behaviour of cells, including their differentiation, proliferation, and turnover. Here we aimed at detailed characterization of the nanostructure of lung ECM and evaluation of its bioactivity on cells grown in vitro. Mouse lungs were decellularized using 0.2 % sodium dodecyl sulphate, hypotonic solutions, and DNase. Morphological analysis of the resulting ECM scaffolds was performed by means of transmission and scanning electron microscopy. The ECM scaffolds retained 3D architecture of the main lung anatomical regions: the alveolar region and the blood/ airway network. The region-specific ECM nanotopology and organization of ECM macromolecules such as fibres of collagen, elastin, and fibrillin were characterized. The lung ECM scaffolds were also homogenized and applied as a supplement to growth medium on primary lung cells in vitro to test the bioactivity of lung ECM. We demonstrate that homogenized ECM does not have a negative impact on the proliferation rate of primary lung cells. In conclusion, we herein show at nanoscale the morphological characteristics of lung ECM and demonstrate that lung ECM produced by decellularization procedure is compatible with in vitro cultured lung cells. These findings add to a better understanding of cells with their natural environment and can be valuable when designing applications of ECM for purposes in tissue engineering.
Links
GJ16-20031Y, research and development projectName: Signalizace FGF ve fibroblastech mléčné žlázy a její úloha ve vývoji a nádorech mléčné žlázy
Investor: Czech Science Foundation
LD15144, research and development projectName: Buněčné a nebuněčné základy pro regeneraci kostí a zubů (Acronym: TissueENG)
Investor: Ministry of Education, Youth and Sports of the CR
LM2015062, research and development projectName: Národní infrastruktura pro biologické a medicínské zobrazování
Investor: Ministry of Education, Youth and Sports of the CR
MUNI/A/1369/2016, interní kód MUName: Zdroje pro tkáňové inženýrství 7 (Acronym: TissueENG 7)
Investor: Masaryk University, Category A
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