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Tytuł pozycji:

Generation of Hepatobiliary Cell Lineages from Human Induced Pluripotent Stem Cells: Applications in Disease Modeling and Drug Screening.

Tytuł:
Generation of Hepatobiliary Cell Lineages from Human Induced Pluripotent Stem Cells: Applications in Disease Modeling and Drug Screening.
Autorzy:
Pasqua M; Fondazione Ri.MED, 90133 Palermo, Italy.
Di Gesù R; Fondazione Ri.MED, 90133 Palermo, Italy.
Chinnici CM; Fondazione Ri.MED, 90133 Palermo, Italy.; Dipartimento della Ricerca, IRCCS ISMETT, 90127 Palermo, Italy.
Conaldi PG; Dipartimento della Ricerca, IRCCS ISMETT, 90127 Palermo, Italy.
Francipane MG; Fondazione Ri.MED, 90133 Palermo, Italy.; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15219, USA.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Jul 30; Vol. 22 (15). Date of Electronic Publication: 2021 Jul 30.
Typ publikacji:
Journal Article; Review
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, [2000-
MeSH Terms:
Cellular Reprogramming Techniques/*methods
Digestive System Diseases/*therapy
Drug Discovery/*methods
Hepatocytes/*cytology
Induced Pluripotent Stem Cells/*cytology
Precision Medicine/*methods
Animals ; Cell Lineage ; Digestive System Diseases/metabolism ; Digestive System Diseases/pathology ; Hepatocytes/metabolism ; Humans ; Tissue Engineering/methods
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Contributed Indexing:
Keywords: cholangiocytes; disease modeling; drug testing; hepatocytes; iPSCs; tissue engineering
Entry Date(s):
Date Created: 20210807 Date Completed: 20210910 Latest Revision: 20231101
Update Code:
20240105
PubMed Central ID:
PMC8348238
DOI:
10.3390/ijms22158227
PMID:
34360991
Czasopismo naukowe
The possibility to reproduce key tissue functions in vitro from induced pluripotent stem cells (iPSCs) is offering an incredible opportunity to gain better insight into biological mechanisms underlying development and disease, and a tool for the rapid screening of drug candidates. This review attempts to summarize recent strategies for specification of iPSCs towards hepatobiliary lineages -hepatocytes and cholangiocytes-and their use as platforms for disease modeling and drug testing. The application of different tissue-engineering methods to promote accurate and reliable readouts is discussed. Space is given to open questions, including to what extent these novel systems can be informative. Potential pathways for improvement are finally suggested.
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