Options for modeling the respiratory system: inserts, scaffolds
and microfluidic chips

J 2019

Options for modeling the respiratory system: inserts, scaffolds and microfluidic chips

SEDLÁKOVÁ, Veronika, Michaela KLOUČKOVÁ, Zuzana GARLÍKOVÁ, Kateřina VAŠÍČKOVÁ, Josef JAROŠ et. al.

Základní údaje

Originální název

Options for modeling the respiratory system: inserts, scaffolds and microfluidic chips

Autoři

SEDLÁKOVÁ, Veronika (203 Česká republika, garant, domácí), Michaela KLOUČKOVÁ (203 Česká republika, domácí), Zuzana GARLÍKOVÁ (203 Česká republika, domácí), Kateřina VAŠÍČKOVÁ (203 Česká republika, domácí), Josef JAROŠ (203 Česká republika, domácí), Mário KANDRA (703 Slovensko, domácí), Hana KOTASOVÁ (203 Česká republika, domácí) a Aleš HAMPL (203 Česká republika, domácí)

Vydání

Drug Discovery Today, Oxford (England), Elsevier Sci Ltd. 2019, 1359-6446

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30104 Pharmacology and pharmacy

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 7.321

Kód RIV

RIV/00216224:14110/19:00108503

Organizační jednotka

Lékařská fakulta

DOI

http://dx.doi.org/10.1016/j.drudis.2019.03.006

UT WoS

000467511200007

Klíčová slova anglicky

On-a-Chip; Alveolar-Capillary Barrier; In-vitro Model; Airway Wall; Extracellular-Matrix; Endothelial-Cells; Epithelial-Cells; High-Throughput; Stem-Cells; Lung

Štítky

14110517, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 14. 4. 2020 14:29, Mgr. Tereza Miškechová

Anotace

V originále

The human respiratory system is continuously exposed to varying levels of hazardous substances ranging from environmental toxins to purposely administered drugs. If the noxious effects exceed the inherent regenerative capacity of the respiratory system, injured tissue undergoes complex remodeling that can significantly affect lung function and lead to various diseases. Advanced near-to-native in vitro lung models are required to understand the mechanisms involved in pulmonary damage and repair and to reliably test the toxicity of compounds to lung tissue. This review is an overview of the development of in vitro respiratory system models used for study of lung diseases. It includes discussion of using these models for environmental toxin assessment and pulmonary toxicity screening.

Návaznosti

MUNI/A/1298/2017, interní kód MU

Název: Zdroje pro tkáňové inženýrství 8 (Akronym: TissueEng 8)

Investor: Masarykova univerzita, Zdroje pro tkáňové inženýrství 8, DO R. 2020_Kategorie A - Specifický výzkum - Studentské výzkumné projekty

MUNI/A/1565/2018, interní kód MU

Název: Zdroje pro tkáňové inženýrství 9 (Akronym: TissueEng 9)

Investor: Masarykova univerzita, Zdroje pro tkáňové inženýrství 9, DO R. 2020_Kategorie A - Specifický výzkum - Studentské výzkumné projekty

NV16-31501A, projekt VaV

Název: Tkáňové inženýrství epitelů: Buňky a protokoly pro regenerativní medicínu

Citovat

SEDLÁKOVÁ, Veronika, Michaela KLOUČKOVÁ, Zuzana GARLÍKOVÁ, Kateřina VAŠÍČKOVÁ, Josef JAROŠ, Mário KANDRA, Hana KOTASOVÁ a Aleš HAMPL. Options for modeling the respiratory system: inserts, scaffolds and microfluidic chips. Drug Discovery Today. Oxford (England): Elsevier Sci Ltd., 2019, roč. 24, č. 4, s. 971-982. ISSN 1359-6446. Dostupné z: https://dx.doi.org/10.1016/j.drudis.2019.03.006.

@article{1550215,
   author = {Sedláková, Veronika and Kloučková, Michaela and Garlíková, Zuzana and Vašíčková, Kateřina and Jaroš, Josef and Kandra, Mário and Kotasová, Hana and Hampl, Aleš},
   article_location = {Oxford (England)},
   article_number = {4},
   doi = {http://dx.doi.org/10.1016/j.drudis.2019.03.006},
   keywords = {On-a-Chip; Alveolar-Capillary Barrier; In-vitro Model; Airway Wall; Extracellular-Matrix; Endothelial-Cells; Epithelial-Cells; High-Throughput; Stem-Cells; Lung},
   language = {eng},
   issn = {1359-6446},
   journal = {Drug Discovery Today},
   title = {Options for modeling the respiratory system: inserts, scaffolds and microfluidic chips},
   url = {https://www.sciencedirect.com/science/article/pii/S1359644618304458?via%3Dihub},
   volume = {24},
   year = {2019}
}

TY  - JOUR
ID  - 1550215
AU  - Sedláková, Veronika - Kloučková, Michaela - Garlíková, Zuzana - Vašíčková, Kateřina - Jaroš, Josef - Kandra, Mário - Kotasová, Hana - Hampl, Aleš
PY  - 2019
TI  - Options for modeling the respiratory system: inserts, scaffolds and microfluidic chips
JF  - Drug Discovery Today
VL  - 24
IS  - 4
SP  - 971-982
EP  - 971-982
PB  - Elsevier Sci Ltd.
SN  - 13596446
KW  - On-a-Chip
KW  - Alveolar-Capillary Barrier
KW  - In-vitro Model
KW  - Airway Wall
KW  - Extracellular-Matrix
KW  - Endothelial-Cells
KW  - Epithelial-Cells
KW  - High-Throughput
KW  - Stem-Cells
KW  - Lung
UR  - https://www.sciencedirect.com/science/article/pii/S1359644618304458?via%3Dihub
L2  - https://www.sciencedirect.com/science/article/pii/S1359644618304458?via%3Dihub
N2  - The human respiratory system is continuously exposed to varying levels of hazardous substances ranging from environmental toxins to purposely administered drugs. If the noxious effects exceed the inherent regenerative capacity of the respiratory system, injured tissue undergoes complex remodeling that can significantly affect lung function and lead to various diseases. Advanced near-to-native in vitro lung models are required to understand the mechanisms involved in pulmonary damage and repair and to reliably test the toxicity of compounds to lung tissue. This review is an overview of the development of in vitro respiratory system models used for study of lung diseases. It includes discussion of using these models for environmental toxin assessment and pulmonary toxicity screening.
ER  -

SEDLÁKOVÁ, Veronika, Michaela KLOUČKOVÁ, Zuzana GARLÍKOVÁ, Kateřina VAŠÍČKOVÁ, Josef JAROŠ, Mário KANDRA, Hana KOTASOVÁ a Aleš HAMPL. Options for modeling the respiratory system: inserts, scaffolds and microfluidic chips. \textit{Drug Discovery Today}. Oxford (England): Elsevier Sci Ltd., 2019, roč.~24, č.~4, s.~971-982. ISSN~1359-6446. Dostupné z: https://dx.doi.org/10.1016/j.drudis.2019.03.006.

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