Cargando…
Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals
Epithelial homeostasis requires the precise balance of epithelial stem/progenitor proliferation and differentiation. While many signaling pathways that regulate epithelial stem cells have been identified, it is probable that other regulators remain unidentified. Here, we use gene-expression profilin...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275525/ https://www.ncbi.nlm.nih.gov/pubmed/30404917 http://dx.doi.org/10.1073/pnas.1719169115 |
_version_ | 1783377823407276032 |
---|---|
author | Doupé, David P. Marshall, Owen J. Dayton, Hannah Brand, Andrea H. Perrimon, Norbert |
author_facet | Doupé, David P. Marshall, Owen J. Dayton, Hannah Brand, Andrea H. Perrimon, Norbert |
author_sort | Doupé, David P. |
collection | PubMed |
description | Epithelial homeostasis requires the precise balance of epithelial stem/progenitor proliferation and differentiation. While many signaling pathways that regulate epithelial stem cells have been identified, it is probable that other regulators remain unidentified. Here, we use gene-expression profiling by targeted DamID to identify the stem/progenitor-specific transcription and signaling factors in the Drosophila midgut. Many signaling pathway components, including ligands of most major pathways, exhibit stem/progenitor-specific expression and have regulatory regions bound by both intrinsic and extrinsic transcription factors. In addition to previously identified stem/progenitor-derived ligands, we show that both the insulin-like factor Ilp6 and TNF ligand eiger are specifically expressed in the stem/progenitors and regulate normal tissue homeostasis. We propose that intestinal stem cells not only integrate multiple signals but also contribute to and regulate the homeostatic signaling microenvironmental niche through the expression of autocrine and paracrine factors. |
format | Online Article Text |
id | pubmed-6275525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-62755252018-12-05 Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals Doupé, David P. Marshall, Owen J. Dayton, Hannah Brand, Andrea H. Perrimon, Norbert Proc Natl Acad Sci U S A Biological Sciences Epithelial homeostasis requires the precise balance of epithelial stem/progenitor proliferation and differentiation. While many signaling pathways that regulate epithelial stem cells have been identified, it is probable that other regulators remain unidentified. Here, we use gene-expression profiling by targeted DamID to identify the stem/progenitor-specific transcription and signaling factors in the Drosophila midgut. Many signaling pathway components, including ligands of most major pathways, exhibit stem/progenitor-specific expression and have regulatory regions bound by both intrinsic and extrinsic transcription factors. In addition to previously identified stem/progenitor-derived ligands, we show that both the insulin-like factor Ilp6 and TNF ligand eiger are specifically expressed in the stem/progenitors and regulate normal tissue homeostasis. We propose that intestinal stem cells not only integrate multiple signals but also contribute to and regulate the homeostatic signaling microenvironmental niche through the expression of autocrine and paracrine factors. National Academy of Sciences 2018-11-27 2018-11-07 /pmc/articles/PMC6275525/ /pubmed/30404917 http://dx.doi.org/10.1073/pnas.1719169115 Text en Copyright © 2018 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Doupé, David P. Marshall, Owen J. Dayton, Hannah Brand, Andrea H. Perrimon, Norbert Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
title | Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
title_full | Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
title_fullStr | Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
title_full_unstemmed | Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
title_short | Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
title_sort | drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275525/ https://www.ncbi.nlm.nih.gov/pubmed/30404917 http://dx.doi.org/10.1073/pnas.1719169115 |
work_keys_str_mv | AT doupedavidp drosophilaintestinalstemandprogenitorcellsaremajorsourcesandregulatorsofhomeostaticnichesignals AT marshallowenj drosophilaintestinalstemandprogenitorcellsaremajorsourcesandregulatorsofhomeostaticnichesignals AT daytonhannah drosophilaintestinalstemandprogenitorcellsaremajorsourcesandregulatorsofhomeostaticnichesignals AT brandandreah drosophilaintestinalstemandprogenitorcellsaremajorsourcesandregulatorsofhomeostaticnichesignals AT perrimonnorbert drosophilaintestinalstemandprogenitorcellsaremajorsourcesandregulatorsofhomeostaticnichesignals |