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Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum
Human breast milk (HBM) provides essential nutrients for newborn growth and development, and contains a variety of biologically active ingredients that can affect gastrointestinal tract and immune system development in breastfed infants. HBM also contains mRNAs, microRNAs and lncRNAs, most of which...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8109075/ https://www.ncbi.nlm.nih.gov/pubmed/33820870 http://dx.doi.org/10.18632/aging.202806 |
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author | Zhou, Yahui Yu, Zhangbin Wang, Xingyun Chen, Wenjuan Liu, Yiwen Zhang, Yinghui Yin, Jing Han, Shuping |
author_facet | Zhou, Yahui Yu, Zhangbin Wang, Xingyun Chen, Wenjuan Liu, Yiwen Zhang, Yinghui Yin, Jing Han, Shuping |
author_sort | Zhou, Yahui |
collection | PubMed |
description | Human breast milk (HBM) provides essential nutrients for newborn growth and development, and contains a variety of biologically active ingredients that can affect gastrointestinal tract and immune system development in breastfed infants. HBM also contains mRNAs, microRNAs and lncRNAs, most of which are encapsulated in milk-derived exosomes and exhibit various important infant development related biological functions. While previous studies have shown that exosomal circRNAs are involved in the intestinal epithelial cells’ proliferation and repair. However, the effect of HBM exosomal circRNAs on intestinal development is not clear. In this study, we identified 6756 circRNAs both in preterm colostrum (PC) and term colostrum (TC), of which 66 were upregulated, and 42 were downregulated (|fold change>2|, p < 0.05) in PC. Pathway analysis showed that the VEGF signalling pathway was involved, and network analysis revealed that the differentially expressed circRNAs bound various miRNAs. Further analyses showed that has_circRNA_405708 and has_circRNA_104707 were involved in the VEGF signalling pathway, and that they all bound various mirRNAs. Exosomes found in preterm colostrum (PC) and term colostrum (TC) promoted VEGF protein expression and induced the proliferation and migration of small intestinal epithelial cells (FHCs). Exosomal circRNAs found in human colostrum (HC) binding to related miRNAs may regulate VEGF signalling, and intestinal development. |
format | Online Article Text |
id | pubmed-8109075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-81090752021-05-12 Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum Zhou, Yahui Yu, Zhangbin Wang, Xingyun Chen, Wenjuan Liu, Yiwen Zhang, Yinghui Yin, Jing Han, Shuping Aging (Albany NY) Research Paper Human breast milk (HBM) provides essential nutrients for newborn growth and development, and contains a variety of biologically active ingredients that can affect gastrointestinal tract and immune system development in breastfed infants. HBM also contains mRNAs, microRNAs and lncRNAs, most of which are encapsulated in milk-derived exosomes and exhibit various important infant development related biological functions. While previous studies have shown that exosomal circRNAs are involved in the intestinal epithelial cells’ proliferation and repair. However, the effect of HBM exosomal circRNAs on intestinal development is not clear. In this study, we identified 6756 circRNAs both in preterm colostrum (PC) and term colostrum (TC), of which 66 were upregulated, and 42 were downregulated (|fold change>2|, p < 0.05) in PC. Pathway analysis showed that the VEGF signalling pathway was involved, and network analysis revealed that the differentially expressed circRNAs bound various miRNAs. Further analyses showed that has_circRNA_405708 and has_circRNA_104707 were involved in the VEGF signalling pathway, and that they all bound various mirRNAs. Exosomes found in preterm colostrum (PC) and term colostrum (TC) promoted VEGF protein expression and induced the proliferation and migration of small intestinal epithelial cells (FHCs). Exosomal circRNAs found in human colostrum (HC) binding to related miRNAs may regulate VEGF signalling, and intestinal development. Impact Journals 2021-04-04 /pmc/articles/PMC8109075/ /pubmed/33820870 http://dx.doi.org/10.18632/aging.202806 Text en Copyright: © 2021 Zhou et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zhou, Yahui Yu, Zhangbin Wang, Xingyun Chen, Wenjuan Liu, Yiwen Zhang, Yinghui Yin, Jing Han, Shuping Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum |
title | Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum |
title_full | Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum |
title_fullStr | Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum |
title_full_unstemmed | Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum |
title_short | Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum |
title_sort | exosomal circrnas contribute to intestinal development via the vegf signalling pathway in human term and preterm colostrum |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8109075/ https://www.ncbi.nlm.nih.gov/pubmed/33820870 http://dx.doi.org/10.18632/aging.202806 |
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