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Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish

Understanding the biological function of amyloid beta (Aβ) precursor protein (APP) beyond its role in Alzheimer’s disease is emerging. Yet, its function during embryonic development is poorly understood. The zebrafish APP orthologue, Appb, is strongly expressed during early development but thus far...

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Autores principales: Banote, Rakesh Kumar, Chebli, Jasmine, Şatır, Tuğçe Munise, Varshney, Gaurav K., Camacho, Rafael, Ledin, Johan, Burgess, Shawn M., Abramsson, Alexandra, Zetterberg, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311384/
https://www.ncbi.nlm.nih.gov/pubmed/32576936
http://dx.doi.org/10.1038/s41598-020-66584-8
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author Banote, Rakesh Kumar
Chebli, Jasmine
Şatır, Tuğçe Munise
Varshney, Gaurav K.
Camacho, Rafael
Ledin, Johan
Burgess, Shawn M.
Abramsson, Alexandra
Zetterberg, Henrik
author_facet Banote, Rakesh Kumar
Chebli, Jasmine
Şatır, Tuğçe Munise
Varshney, Gaurav K.
Camacho, Rafael
Ledin, Johan
Burgess, Shawn M.
Abramsson, Alexandra
Zetterberg, Henrik
author_sort Banote, Rakesh Kumar
collection PubMed
description Understanding the biological function of amyloid beta (Aβ) precursor protein (APP) beyond its role in Alzheimer’s disease is emerging. Yet, its function during embryonic development is poorly understood. The zebrafish APP orthologue, Appb, is strongly expressed during early development but thus far has only been studied via morpholino-mediated knockdown. Zebrafish enables analysis of cellular processes in an ontogenic context, which is limited in many other vertebrates. We characterized zebrafish carrying a homozygous mutation that introduces a premature stop in exon 2 of the appb gene. We report that appb mutants are significantly smaller until 2 dpf and display perturbed enveloping layer (EVL) integrity and cell protrusions at the blastula stage. Moreover, appb mutants surviving beyond 48 hpf exhibited no behavioral defects at 6 dpf and developed into healthy and fertile adults. The expression of the app family member, appa, was also found to be altered in appb mutants. Taken together, we show that appb is involved in the initial development of zebrafish by supporting the integrity of the EVL, likely by mediating cell adhesion properties. The loss of Appb might then be compensated for by other app family members to maintain normal development.
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spelling pubmed-73113842020-06-25 Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish Banote, Rakesh Kumar Chebli, Jasmine Şatır, Tuğçe Munise Varshney, Gaurav K. Camacho, Rafael Ledin, Johan Burgess, Shawn M. Abramsson, Alexandra Zetterberg, Henrik Sci Rep Article Understanding the biological function of amyloid beta (Aβ) precursor protein (APP) beyond its role in Alzheimer’s disease is emerging. Yet, its function during embryonic development is poorly understood. The zebrafish APP orthologue, Appb, is strongly expressed during early development but thus far has only been studied via morpholino-mediated knockdown. Zebrafish enables analysis of cellular processes in an ontogenic context, which is limited in many other vertebrates. We characterized zebrafish carrying a homozygous mutation that introduces a premature stop in exon 2 of the appb gene. We report that appb mutants are significantly smaller until 2 dpf and display perturbed enveloping layer (EVL) integrity and cell protrusions at the blastula stage. Moreover, appb mutants surviving beyond 48 hpf exhibited no behavioral defects at 6 dpf and developed into healthy and fertile adults. The expression of the app family member, appa, was also found to be altered in appb mutants. Taken together, we show that appb is involved in the initial development of zebrafish by supporting the integrity of the EVL, likely by mediating cell adhesion properties. The loss of Appb might then be compensated for by other app family members to maintain normal development. Nature Publishing Group UK 2020-06-23 /pmc/articles/PMC7311384/ /pubmed/32576936 http://dx.doi.org/10.1038/s41598-020-66584-8 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Banote, Rakesh Kumar
Chebli, Jasmine
Şatır, Tuğçe Munise
Varshney, Gaurav K.
Camacho, Rafael
Ledin, Johan
Burgess, Shawn M.
Abramsson, Alexandra
Zetterberg, Henrik
Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
title Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
title_full Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
title_fullStr Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
title_full_unstemmed Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
title_short Amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
title_sort amyloid precursor protein-b facilitates cell adhesion during early development in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311384/
https://www.ncbi.nlm.nih.gov/pubmed/32576936
http://dx.doi.org/10.1038/s41598-020-66584-8
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