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The preparation of decellularized mouse lung matrix scaffolds for analysis of lung regenerative cell potential.
In: Mouse Cell Culture. Berlin [u.a.]: Springer, 2019. 275-295 (Methods Mol. Biol. ; 1940)
Lung transplantation is the only option for patients with end-stage lung disease, but there is a shortage of available lung donors. Furthermore, efficiency of lung transplantation has been limited due to primary graft dysfunction. Recent mouse models mimicking lung disease in humans have allowed for deepening our understanding of disease pathomechanisms. Moreover, new techniques such as decellularization and recellularization have opened up new possibilities to contribute to our understanding of the regenerative mechanisms involved in the lung. Stripping the lung of its native cells allows for unprecedented analyses of extracellular matrix and sets a physiologic platform to study the regenerative potential of seeded cells. A comprehensive understanding of the molecular pathways involved for lung development and regeneration in mouse models can be translated to regeneration strategies in higher organisms, including humans. Here we describe and discuss several techniques used for murine lung de- and recellularization, methods for evaluation of efficacy including histology, protein/RNA isolation at the whole lung, as well as lung slices level.
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Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Sammelbandbeitrag/Buchkapitel
Schlagwörter
Biomaterial ; Decellularization ; Lung ; Precision Cut Lung Slices ; Recellularization ; Scaffold ; Tissue Engineering
Sprache
englisch
Veröffentlichungsjahr
2019
HGF-Berichtsjahr
2019
ISSN (print) / ISBN
1064-3745
e-ISSN
1940-6029
Bandtitel
Mouse Cell Culture
Zeitschrift
Methods in Molecular Biology
Quellenangaben
Band: 1940,
Seiten: 275-295
Verlag
Springer
Verlagsort
Berlin [u.a.]
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Lung Health and Immunity (LHI)
POF Topic(s)
30202 - Environmental Health
Forschungsfeld(er)
Lung Research
PSP-Element(e)
G-505000-008
Scopus ID
85061998624
PubMed ID
30788833
Erfassungsdatum
2019-03-15