Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology

Nuclear receptors (NRs) are ligand-activated transcription factors regulating a large variety of processes involved in reproduction, development, and metabolism. NRs are ideal drug targets because they are activated by lipophilic ligands that easily pass cell membranes. Immortalized cell lines recapitulate NR biology poorly and generating primary cultures is laborious and requires a constant need for donor material. There is a clear need for development of novel preclinical model systems that better resemble human physiology. Uncertainty due to technical limitations early in drug development is often the cause of preclinical drugs not reaching the clinic. Here, we studied whether organoids, mini-organs derived from the respective mouse tissue's stem cells, can serve as a novel model system to study NR biology and targetability. We characterized mRNA expression profiles of the NR superfamily in mouse liver, ileum, and colon organoids. Tissue-specific expression patterns were largely maintained in the organoids, indicating their suitability for NR research. Metabolic NRs Fxrα, Lxrα, Lxrβ, Pparα, and Pparγ induced expression of and binding to endogenous target genes. Transcriptome analyses of wildtype colon organoids stimulated with Rosiglitazone showed that lipid metabolism was the highest significant changed function, greatly mimicking the PPARs and Rosiglitazone function in vivo. Finally, using organoids we identify Trpm6, Slc26a3, Ang1, and Rnase4, as novel Fxr target genes. Our results demonstrate that organoids represent a framework to study NR biology that can be further expanded to human organoids to improve preclinical testing of novel drugs that target this pharmacologically important class of ligand activated transcription factors.

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Main Authors: Bijsmans, Ingrid T.G.W., Milona, Alexandra, Ijssennagger, Noortje, Willemsen, Ellen C.L., Ramos Pittol, José M., Jonker, Johan W., Lange, Katja, Hooiveld, Guido J.E.J., van Mil, Saskia W.C.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:Fxr, Ligands, Lxr, Nuclear receptors, Organoids, Ppar,
Online Access:https://research.wur.nl/en/publications/characterization-of-stem-cell-derived-liver-and-intestinal-organo
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spelling dig-wur-nl-wurpubs-5119282025-01-17 Bijsmans, Ingrid T.G.W. Milona, Alexandra Ijssennagger, Noortje Willemsen, Ellen C.L. Ramos Pittol, José M. Jonker, Johan W. Lange, Katja Hooiveld, Guido J.E.J. van Mil, Saskia W.C. Article/Letter to editor Biochimica et Biophysica Acta. Molecular Basis of Disease 1863 (2017) 3 ISSN: 0925-4439 Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology 2017 Nuclear receptors (NRs) are ligand-activated transcription factors regulating a large variety of processes involved in reproduction, development, and metabolism. NRs are ideal drug targets because they are activated by lipophilic ligands that easily pass cell membranes. Immortalized cell lines recapitulate NR biology poorly and generating primary cultures is laborious and requires a constant need for donor material. There is a clear need for development of novel preclinical model systems that better resemble human physiology. Uncertainty due to technical limitations early in drug development is often the cause of preclinical drugs not reaching the clinic. Here, we studied whether organoids, mini-organs derived from the respective mouse tissue's stem cells, can serve as a novel model system to study NR biology and targetability. We characterized mRNA expression profiles of the NR superfamily in mouse liver, ileum, and colon organoids. Tissue-specific expression patterns were largely maintained in the organoids, indicating their suitability for NR research. Metabolic NRs Fxrα, Lxrα, Lxrβ, Pparα, and Pparγ induced expression of and binding to endogenous target genes. Transcriptome analyses of wildtype colon organoids stimulated with Rosiglitazone showed that lipid metabolism was the highest significant changed function, greatly mimicking the PPARs and Rosiglitazone function in vivo. Finally, using organoids we identify Trpm6, Slc26a3, Ang1, and Rnase4, as novel Fxr target genes. Our results demonstrate that organoids represent a framework to study NR biology that can be further expanded to human organoids to improve preclinical testing of novel drugs that target this pharmacologically important class of ligand activated transcription factors. en application/pdf https://research.wur.nl/en/publications/characterization-of-stem-cell-derived-liver-and-intestinal-organo 10.1016/j.bbadis.2016.12.004 https://edepot.wur.nl/403699 Fxr Ligands Lxr Nuclear receptors Organoids Ppar (c) publisher Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic Fxr
Ligands
Lxr
Nuclear receptors
Organoids
Ppar
Fxr
Ligands
Lxr
Nuclear receptors
Organoids
Ppar
spellingShingle Fxr
Ligands
Lxr
Nuclear receptors
Organoids
Ppar
Fxr
Ligands
Lxr
Nuclear receptors
Organoids
Ppar
Bijsmans, Ingrid T.G.W.
Milona, Alexandra
Ijssennagger, Noortje
Willemsen, Ellen C.L.
Ramos Pittol, José M.
Jonker, Johan W.
Lange, Katja
Hooiveld, Guido J.E.J.
van Mil, Saskia W.C.
Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
description Nuclear receptors (NRs) are ligand-activated transcription factors regulating a large variety of processes involved in reproduction, development, and metabolism. NRs are ideal drug targets because they are activated by lipophilic ligands that easily pass cell membranes. Immortalized cell lines recapitulate NR biology poorly and generating primary cultures is laborious and requires a constant need for donor material. There is a clear need for development of novel preclinical model systems that better resemble human physiology. Uncertainty due to technical limitations early in drug development is often the cause of preclinical drugs not reaching the clinic. Here, we studied whether organoids, mini-organs derived from the respective mouse tissue's stem cells, can serve as a novel model system to study NR biology and targetability. We characterized mRNA expression profiles of the NR superfamily in mouse liver, ileum, and colon organoids. Tissue-specific expression patterns were largely maintained in the organoids, indicating their suitability for NR research. Metabolic NRs Fxrα, Lxrα, Lxrβ, Pparα, and Pparγ induced expression of and binding to endogenous target genes. Transcriptome analyses of wildtype colon organoids stimulated with Rosiglitazone showed that lipid metabolism was the highest significant changed function, greatly mimicking the PPARs and Rosiglitazone function in vivo. Finally, using organoids we identify Trpm6, Slc26a3, Ang1, and Rnase4, as novel Fxr target genes. Our results demonstrate that organoids represent a framework to study NR biology that can be further expanded to human organoids to improve preclinical testing of novel drugs that target this pharmacologically important class of ligand activated transcription factors.
format Article/Letter to editor
topic_facet Fxr
Ligands
Lxr
Nuclear receptors
Organoids
Ppar
author Bijsmans, Ingrid T.G.W.
Milona, Alexandra
Ijssennagger, Noortje
Willemsen, Ellen C.L.
Ramos Pittol, José M.
Jonker, Johan W.
Lange, Katja
Hooiveld, Guido J.E.J.
van Mil, Saskia W.C.
author_facet Bijsmans, Ingrid T.G.W.
Milona, Alexandra
Ijssennagger, Noortje
Willemsen, Ellen C.L.
Ramos Pittol, José M.
Jonker, Johan W.
Lange, Katja
Hooiveld, Guido J.E.J.
van Mil, Saskia W.C.
author_sort Bijsmans, Ingrid T.G.W.
title Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
title_short Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
title_full Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
title_fullStr Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
title_full_unstemmed Characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
title_sort characterization of stem cell-derived liver and intestinal organoids as a model system to study nuclear receptor biology
url https://research.wur.nl/en/publications/characterization-of-stem-cell-derived-liver-and-intestinal-organo
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