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spelling ftfrontimediafig:oai:figshare.com:article/14533254 2023-05-15T15:30:56+02:00 Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx Alexander C. West Yasutaka Mizoro Shona H. Wood Louise M. Ince Marianne Iversen Even H. Jørgensen Torfinn Nome Simen Rød Sandve Samuel A. M. Martin Andrew S. I. Loudon David G. Hazlerigg 2021-05-04T04:48:54Z https://doi.org/10.3389/fimmu.2021.669889.s002 https://figshare.com/articles/dataset/Table_1_Immunologic_Profiling_of_the_Atlantic_Salmon_Gill_by_Single_Nuclei_Transcriptomics_xlsx/14533254 unknown doi:10.3389/fimmu.2021.669889.s002 https://figshare.com/articles/dataset/Table_1_Immunologic_Profiling_of_the_Atlantic_Salmon_Gill_by_Single_Nuclei_Transcriptomics_xlsx/14533254 CC BY 4.0 CC-BY Immunology Applied Immunology (incl. Antibody Engineering Xenotransplantation and T-cell Therapies) Autoimmunity Cellular Immunology Humoural Immunology and Immunochemistry Immunogenetics (incl. Genetic Immunology) Innate Immunity Transplantation Immunology Tumour Immunology Immunology not elsewhere classified Genetic Immunology Animal Immunology Veterinary Immunology Atlantic salmon (Salmo salar) smoltification photoperiod immune cells gill single nuclei RNA sequencing Dataset 2021 ftfrontimediafig https://doi.org/10.3389/fimmu.2021.669889.s002 2021-05-05T22:57:53Z Anadromous salmonids begin life adapted to the freshwater environments of their natal streams before a developmental transition, known as smoltification, transforms them into marine-adapted fish. In the wild, smoltification is a photoperiod-regulated process, involving radical remodeling of gill function to cope with the profound osmotic and immunological challenges of seawater (SW) migration. While prior work has highlighted the role of specialized “mitochondrion-rich” cells (MRCs) and accessory cells (ACs) in delivering this phenotype, recent RNA profiling experiments suggest that remodeling is far more extensive than previously appreciated. Here, we use single-nuclei RNAseq to characterize the extent of cytological changes in the gill of Atlantic salmon during smoltification and SW transfer. We identify 20 distinct cell clusters, including known, but also novel gill cell types. These data allow us to isolate cluster-specific, smoltification-associated changes in gene expression and to describe how the cellular make-up of the gill changes through smoltification. As expected, we noted an increase in the proportion of seawater mitochondrion-rich cells, however, we also identify previously unknown reduction of several immune-related cell types. Overall, our results provide fresh detail of the cellular complexity in the gill and suggest that smoltification triggers unexpected immune reprogramming. Dataset Atlantic salmon Salmo salar Frontiers: Figshare
institution Open Polar
collection Frontiers: Figshare
op_collection_id ftfrontimediafig
language unknown
topic Immunology
Applied Immunology (incl. Antibody Engineering
Xenotransplantation and T-cell Therapies)
Autoimmunity
Cellular Immunology
Humoural Immunology and Immunochemistry
Immunogenetics (incl. Genetic Immunology)
Innate Immunity
Transplantation Immunology
Tumour Immunology
Immunology not elsewhere classified
Genetic Immunology
Animal Immunology
Veterinary Immunology
Atlantic salmon (Salmo salar)
smoltification
photoperiod
immune cells
gill
single nuclei RNA sequencing
spellingShingle Immunology
Applied Immunology (incl. Antibody Engineering
Xenotransplantation and T-cell Therapies)
Autoimmunity
Cellular Immunology
Humoural Immunology and Immunochemistry
Immunogenetics (incl. Genetic Immunology)
Innate Immunity
Transplantation Immunology
Tumour Immunology
Immunology not elsewhere classified
Genetic Immunology
Animal Immunology
Veterinary Immunology
Atlantic salmon (Salmo salar)
smoltification
photoperiod
immune cells
gill
single nuclei RNA sequencing
Alexander C. West
Yasutaka Mizoro
Shona H. Wood
Louise M. Ince
Marianne Iversen
Even H. Jørgensen
Torfinn Nome
Simen Rød Sandve
Samuel A. M. Martin
Andrew S. I. Loudon
David G. Hazlerigg
Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx
topic_facet Immunology
Applied Immunology (incl. Antibody Engineering
Xenotransplantation and T-cell Therapies)
Autoimmunity
Cellular Immunology
Humoural Immunology and Immunochemistry
Immunogenetics (incl. Genetic Immunology)
Innate Immunity
Transplantation Immunology
Tumour Immunology
Immunology not elsewhere classified
Genetic Immunology
Animal Immunology
Veterinary Immunology
Atlantic salmon (Salmo salar)
smoltification
photoperiod
immune cells
gill
single nuclei RNA sequencing
description Anadromous salmonids begin life adapted to the freshwater environments of their natal streams before a developmental transition, known as smoltification, transforms them into marine-adapted fish. In the wild, smoltification is a photoperiod-regulated process, involving radical remodeling of gill function to cope with the profound osmotic and immunological challenges of seawater (SW) migration. While prior work has highlighted the role of specialized “mitochondrion-rich” cells (MRCs) and accessory cells (ACs) in delivering this phenotype, recent RNA profiling experiments suggest that remodeling is far more extensive than previously appreciated. Here, we use single-nuclei RNAseq to characterize the extent of cytological changes in the gill of Atlantic salmon during smoltification and SW transfer. We identify 20 distinct cell clusters, including known, but also novel gill cell types. These data allow us to isolate cluster-specific, smoltification-associated changes in gene expression and to describe how the cellular make-up of the gill changes through smoltification. As expected, we noted an increase in the proportion of seawater mitochondrion-rich cells, however, we also identify previously unknown reduction of several immune-related cell types. Overall, our results provide fresh detail of the cellular complexity in the gill and suggest that smoltification triggers unexpected immune reprogramming.
format Dataset
author Alexander C. West
Yasutaka Mizoro
Shona H. Wood
Louise M. Ince
Marianne Iversen
Even H. Jørgensen
Torfinn Nome
Simen Rød Sandve
Samuel A. M. Martin
Andrew S. I. Loudon
David G. Hazlerigg
author_facet Alexander C. West
Yasutaka Mizoro
Shona H. Wood
Louise M. Ince
Marianne Iversen
Even H. Jørgensen
Torfinn Nome
Simen Rød Sandve
Samuel A. M. Martin
Andrew S. I. Loudon
David G. Hazlerigg
author_sort Alexander C. West
title Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx
title_short Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx
title_full Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx
title_fullStr Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx
title_full_unstemmed Table_1_Immunologic Profiling of the Atlantic Salmon Gill by Single Nuclei Transcriptomics.xlsx
title_sort table_1_immunologic profiling of the atlantic salmon gill by single nuclei transcriptomics.xlsx
publishDate 2021
url https://doi.org/10.3389/fimmu.2021.669889.s002
https://figshare.com/articles/dataset/Table_1_Immunologic_Profiling_of_the_Atlantic_Salmon_Gill_by_Single_Nuclei_Transcriptomics_xlsx/14533254
genre Atlantic salmon
Salmo salar
genre_facet Atlantic salmon
Salmo salar
op_relation doi:10.3389/fimmu.2021.669889.s002
https://figshare.com/articles/dataset/Table_1_Immunologic_Profiling_of_the_Atlantic_Salmon_Gill_by_Single_Nuclei_Transcriptomics_xlsx/14533254
op_rights CC BY 4.0
op_rightsnorm CC-BY
op_doi https://doi.org/10.3389/fimmu.2021.669889.s002
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