Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes

Abstract Background Endocrine cells of the zebrafish digestive system play an important role in regulating metabolism and include pancreatic endocrine cells (PECs) clustered in the islets of Langerhans and the enteroendocrine cells (EECs) scattered in the intestinal epithelium. Despite EECs and PECs...

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Main Authors: Arnaud Lavergne, Estefania Tarifeño-Saldivia, Justine Pirson, Anne-Sophie Reuter, Lydie Flasse, Isabelle Manfroid, Marianne L. Voz, Bernard Peers
Format: Article
Language:English
Published: BMC 2020-08-01
Series:BMC Biology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12915-020-00840-1
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author Arnaud Lavergne
Estefania Tarifeño-Saldivia
Justine Pirson
Anne-Sophie Reuter
Lydie Flasse
Isabelle Manfroid
Marianne L. Voz
Bernard Peers
author_facet Arnaud Lavergne
Estefania Tarifeño-Saldivia
Justine Pirson
Anne-Sophie Reuter
Lydie Flasse
Isabelle Manfroid
Marianne L. Voz
Bernard Peers
author_sort Arnaud Lavergne
collection DOAJ
description Abstract Background Endocrine cells of the zebrafish digestive system play an important role in regulating metabolism and include pancreatic endocrine cells (PECs) clustered in the islets of Langerhans and the enteroendocrine cells (EECs) scattered in the intestinal epithelium. Despite EECs and PECs are being located in distinct organs, their differentiation involves shared molecular mechanisms and transcription factors. However, their degree of relatedness remains unexplored. In this study, we investigated comprehensively the similarity of EECs and PECs by defining their transcriptomic landscape and comparing the regulatory programmes controlled by Pax6b, a key player in both EEC and PEC differentiations. Results RNA sequencing was performed on EECs and PECs isolated from wild-type and pax6b mutant zebrafish. Data mining of wild-type zebrafish EEC data confirmed the expression of orthologues for most known mammalian EEC hormones, but also revealed the expression of three additional neuropeptide hormones (Proenkephalin-a, Calcitonin-a and Adcyap1a) not previously reported to be expressed by EECs in any species. Comparison of transcriptomes from EECs, PECs and other zebrafish tissues highlights a very close similarity between EECs and PECs, with more than 70% of genes being expressed in both endocrine cell types. Comparison of Pax6b-regulated genes in EECs and PECs revealed a significant overlap. pax6b loss-of-function does not affect the total number of EECs and PECs but instead disrupts the balance between endocrine cell subtypes, leading to an increase of ghrelin- and motilin-like-expressing cells in both the intestine and pancreas at the expense of other endocrine cells such as beta and delta cells in the pancreas and pyyb-expressing cells in the intestine. Finally, we show that the homeodomain of Pax6b is dispensable for its action in both EECs and PECs. Conclusion We have analysed the transcriptomic landscape of wild-type and pax6b mutant zebrafish EECs and PECs. Our study highlights the close relatedness of EECs and PECs at the transcriptomic and regulatory levels, supporting the hypothesis of a common phylogenetic origin and underscoring the potential implication of EECs in metabolic diseases such as type 2 diabetes.
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spelling doaj.art-583dec2d36a3475d99a771aab9ab63c12022-12-21T19:45:28ZengBMCBMC Biology1741-70072020-08-0118111910.1186/s12915-020-00840-1Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmesArnaud Lavergne0Estefania Tarifeño-Saldivia1Justine Pirson2Anne-Sophie Reuter3Lydie Flasse4Isabelle Manfroid5Marianne L. Voz6Bernard Peers7Laboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeLaboratory of Zebrafish Development and Disease Models (ZDDM), GIGA, University of LiègeAbstract Background Endocrine cells of the zebrafish digestive system play an important role in regulating metabolism and include pancreatic endocrine cells (PECs) clustered in the islets of Langerhans and the enteroendocrine cells (EECs) scattered in the intestinal epithelium. Despite EECs and PECs are being located in distinct organs, their differentiation involves shared molecular mechanisms and transcription factors. However, their degree of relatedness remains unexplored. In this study, we investigated comprehensively the similarity of EECs and PECs by defining their transcriptomic landscape and comparing the regulatory programmes controlled by Pax6b, a key player in both EEC and PEC differentiations. Results RNA sequencing was performed on EECs and PECs isolated from wild-type and pax6b mutant zebrafish. Data mining of wild-type zebrafish EEC data confirmed the expression of orthologues for most known mammalian EEC hormones, but also revealed the expression of three additional neuropeptide hormones (Proenkephalin-a, Calcitonin-a and Adcyap1a) not previously reported to be expressed by EECs in any species. Comparison of transcriptomes from EECs, PECs and other zebrafish tissues highlights a very close similarity between EECs and PECs, with more than 70% of genes being expressed in both endocrine cell types. Comparison of Pax6b-regulated genes in EECs and PECs revealed a significant overlap. pax6b loss-of-function does not affect the total number of EECs and PECs but instead disrupts the balance between endocrine cell subtypes, leading to an increase of ghrelin- and motilin-like-expressing cells in both the intestine and pancreas at the expense of other endocrine cells such as beta and delta cells in the pancreas and pyyb-expressing cells in the intestine. Finally, we show that the homeodomain of Pax6b is dispensable for its action in both EECs and PECs. Conclusion We have analysed the transcriptomic landscape of wild-type and pax6b mutant zebrafish EECs and PECs. Our study highlights the close relatedness of EECs and PECs at the transcriptomic and regulatory levels, supporting the hypothesis of a common phylogenetic origin and underscoring the potential implication of EECs in metabolic diseases such as type 2 diabetes.http://link.springer.com/article/10.1186/s12915-020-00840-1Pancreatic endocrine cellsEnteroendocrineTranscriptomeRNA-seqPax6Zebrafish
spellingShingle Arnaud Lavergne
Estefania Tarifeño-Saldivia
Justine Pirson
Anne-Sophie Reuter
Lydie Flasse
Isabelle Manfroid
Marianne L. Voz
Bernard Peers
Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
BMC Biology
Pancreatic endocrine cells
Enteroendocrine
Transcriptome
RNA-seq
Pax6
Zebrafish
title Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
title_full Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
title_fullStr Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
title_full_unstemmed Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
title_short Pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
title_sort pancreatic and intestinal endocrine cells in zebrafish share common transcriptomic signatures and regulatory programmes
topic Pancreatic endocrine cells
Enteroendocrine
Transcriptome
RNA-seq
Pax6
Zebrafish
url http://link.springer.com/article/10.1186/s12915-020-00840-1
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