Cargando…
Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling
Organoids culture provides unique opportunities to study human diseases and to complement animal models. Several organs and tissues can be in vitro cultured in 3D structures resembling in vivo tissue organization. Organoids culture contains most of the cell types of the original tissue and are maint...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371140/ https://www.ncbi.nlm.nih.gov/pubmed/34404908 http://dx.doi.org/10.1038/s41598-021-96321-8 |
_version_ | 1783739578463551488 |
---|---|
author | Lu, Jing Krepelova, Anna Rasa, Seyed Mohammad Mahdi Annunziata, Francesco Husak, Olena Adam, Lisa Nunna, Suneetha Neri, Francesco |
author_facet | Lu, Jing Krepelova, Anna Rasa, Seyed Mohammad Mahdi Annunziata, Francesco Husak, Olena Adam, Lisa Nunna, Suneetha Neri, Francesco |
author_sort | Lu, Jing |
collection | PubMed |
description | Organoids culture provides unique opportunities to study human diseases and to complement animal models. Several organs and tissues can be in vitro cultured in 3D structures resembling in vivo tissue organization. Organoids culture contains most of the cell types of the original tissue and are maintained by growth factors mimicking the in vivo state. However, the system is yet not fully understood, and specific in vivo features especially those driven by cell-extrinsic factors may be lost in culture. Here we show a comprehensive transcriptome-wide characterization of mouse gut organoids derived from different intestinal compartments and from mice of different gender and age. RNA-seq analysis showed that the in vitro culture strongly influences the global transcriptome of the intestinal epithelial cells (~ 60% of the total variance). Several compartment-, age- and gender-related transcriptome features are lost after culturing indicating that they are driven by niche or systemic factors. However, certain intrinsic transcriptional programs, for example, some compartment-related features and a minority of gender- and aging- related features are maintained in vitro which suggested possibilities for these features to be studied in this system. Moreover, our study provides knowledge about the cell-extrinsic or cell-intrinsic origin of intestinal epithelial transcriptional programs. We anticipated that our characterization of this in vitro system is an important reference for scientists and clinicians using intestinal organoids as a research model. |
format | Online Article Text |
id | pubmed-8371140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83711402021-08-19 Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling Lu, Jing Krepelova, Anna Rasa, Seyed Mohammad Mahdi Annunziata, Francesco Husak, Olena Adam, Lisa Nunna, Suneetha Neri, Francesco Sci Rep Article Organoids culture provides unique opportunities to study human diseases and to complement animal models. Several organs and tissues can be in vitro cultured in 3D structures resembling in vivo tissue organization. Organoids culture contains most of the cell types of the original tissue and are maintained by growth factors mimicking the in vivo state. However, the system is yet not fully understood, and specific in vivo features especially those driven by cell-extrinsic factors may be lost in culture. Here we show a comprehensive transcriptome-wide characterization of mouse gut organoids derived from different intestinal compartments and from mice of different gender and age. RNA-seq analysis showed that the in vitro culture strongly influences the global transcriptome of the intestinal epithelial cells (~ 60% of the total variance). Several compartment-, age- and gender-related transcriptome features are lost after culturing indicating that they are driven by niche or systemic factors. However, certain intrinsic transcriptional programs, for example, some compartment-related features and a minority of gender- and aging- related features are maintained in vitro which suggested possibilities for these features to be studied in this system. Moreover, our study provides knowledge about the cell-extrinsic or cell-intrinsic origin of intestinal epithelial transcriptional programs. We anticipated that our characterization of this in vitro system is an important reference for scientists and clinicians using intestinal organoids as a research model. Nature Publishing Group UK 2021-08-17 /pmc/articles/PMC8371140/ /pubmed/34404908 http://dx.doi.org/10.1038/s41598-021-96321-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lu, Jing Krepelova, Anna Rasa, Seyed Mohammad Mahdi Annunziata, Francesco Husak, Olena Adam, Lisa Nunna, Suneetha Neri, Francesco Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling |
title | Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling |
title_full | Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling |
title_fullStr | Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling |
title_full_unstemmed | Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling |
title_short | Characterization of an in vitro 3D intestinal organoid model by using massive RNAseq-based transcriptome profiling |
title_sort | characterization of an in vitro 3d intestinal organoid model by using massive rnaseq-based transcriptome profiling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371140/ https://www.ncbi.nlm.nih.gov/pubmed/34404908 http://dx.doi.org/10.1038/s41598-021-96321-8 |
work_keys_str_mv | AT lujing characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT krepelovaanna characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT rasaseyedmohammadmahdi characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT annunziatafrancesco characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT husakolena characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT adamlisa characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT nunnasuneetha characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling AT nerifrancesco characterizationofaninvitro3dintestinalorganoidmodelbyusingmassivernaseqbasedtranscriptomeprofiling |