Cargando…
Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate
Colonial tunicates are marine organisms that possess multiple brains simultaneously during their colonial phase. While the cyclical processes of neurogenesis and neurodegeneration characterizing their life cycle have been documented previously, the cellular and molecular changes associated with such...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303981/ https://www.ncbi.nlm.nih.gov/pubmed/35858312 http://dx.doi.org/10.1073/pnas.2203032119 |
_version_ | 1784751998973771776 |
---|---|
author | Anselmi, Chiara Kowarsky, Mark Gasparini, Fabio Caicci, Federico Ishizuka, Katherine J. Palmeri, Karla J. Raveh, Tal Sinha, Rahul Neff, Norma Quake, Stephen R. Weissman, Irving L. Voskoboynik, Ayelet Manni, Lucia |
author_facet | Anselmi, Chiara Kowarsky, Mark Gasparini, Fabio Caicci, Federico Ishizuka, Katherine J. Palmeri, Karla J. Raveh, Tal Sinha, Rahul Neff, Norma Quake, Stephen R. Weissman, Irving L. Voskoboynik, Ayelet Manni, Lucia |
author_sort | Anselmi, Chiara |
collection | PubMed |
description | Colonial tunicates are marine organisms that possess multiple brains simultaneously during their colonial phase. While the cyclical processes of neurogenesis and neurodegeneration characterizing their life cycle have been documented previously, the cellular and molecular changes associated with such processes and their relationship with variation in brain morphology and individual (zooid) behavior throughout adult life remains unknown. Here, we introduce Botryllus schlosseri as an invertebrate model for neurogenesis, neural degeneration, and evolutionary neuroscience. Our analysis reveals that during the weekly colony budding (i.e., asexual reproduction), prior to programmed cell death and removal by phagocytes, decreases in the number of neurons in the adult brain are associated with reduced behavioral response and significant change in the expression of 73 mammalian homologous genes associated with neurodegenerative disease. Similarly, when comparing young colonies (1 to 2 y of age) to those reared in a laboratory for ∼20 y, we found that older colonies contained significantly fewer neurons and exhibited reduced behavioral response alongside changes in the expression of 148 such genes (35 of which were differentially expressed across both timescales). The existence of two distinct yet apparently related neurodegenerative pathways represents a novel platform to study the gene products governing the relationship between aging, neural regeneration and degeneration, and loss of nervous system function. Indeed, as a member of an evolutionary clade considered to be a sister group of vertebrates, this organism may be a fundamental resource in understanding how evolution has shaped these processes across phylogeny and obtaining mechanistic insight. |
format | Online Article Text |
id | pubmed-9303981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-93039812022-07-23 Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate Anselmi, Chiara Kowarsky, Mark Gasparini, Fabio Caicci, Federico Ishizuka, Katherine J. Palmeri, Karla J. Raveh, Tal Sinha, Rahul Neff, Norma Quake, Stephen R. Weissman, Irving L. Voskoboynik, Ayelet Manni, Lucia Proc Natl Acad Sci U S A Biological Sciences Colonial tunicates are marine organisms that possess multiple brains simultaneously during their colonial phase. While the cyclical processes of neurogenesis and neurodegeneration characterizing their life cycle have been documented previously, the cellular and molecular changes associated with such processes and their relationship with variation in brain morphology and individual (zooid) behavior throughout adult life remains unknown. Here, we introduce Botryllus schlosseri as an invertebrate model for neurogenesis, neural degeneration, and evolutionary neuroscience. Our analysis reveals that during the weekly colony budding (i.e., asexual reproduction), prior to programmed cell death and removal by phagocytes, decreases in the number of neurons in the adult brain are associated with reduced behavioral response and significant change in the expression of 73 mammalian homologous genes associated with neurodegenerative disease. Similarly, when comparing young colonies (1 to 2 y of age) to those reared in a laboratory for ∼20 y, we found that older colonies contained significantly fewer neurons and exhibited reduced behavioral response alongside changes in the expression of 148 such genes (35 of which were differentially expressed across both timescales). The existence of two distinct yet apparently related neurodegenerative pathways represents a novel platform to study the gene products governing the relationship between aging, neural regeneration and degeneration, and loss of nervous system function. Indeed, as a member of an evolutionary clade considered to be a sister group of vertebrates, this organism may be a fundamental resource in understanding how evolution has shaped these processes across phylogeny and obtaining mechanistic insight. National Academy of Sciences 2022-07-11 2022-07-19 /pmc/articles/PMC9303981/ /pubmed/35858312 http://dx.doi.org/10.1073/pnas.2203032119 Text en Copyright © 2022 the Author(s). Published by PNAS https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Anselmi, Chiara Kowarsky, Mark Gasparini, Fabio Caicci, Federico Ishizuka, Katherine J. Palmeri, Karla J. Raveh, Tal Sinha, Rahul Neff, Norma Quake, Stephen R. Weissman, Irving L. Voskoboynik, Ayelet Manni, Lucia Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
title | Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
title_full | Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
title_fullStr | Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
title_full_unstemmed | Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
title_short | Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
title_sort | two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303981/ https://www.ncbi.nlm.nih.gov/pubmed/35858312 http://dx.doi.org/10.1073/pnas.2203032119 |
work_keys_str_mv | AT anselmichiara twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT kowarskymark twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT gasparinifabio twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT caiccifederico twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT ishizukakatherinej twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT palmerikarlaj twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT ravehtal twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT sinharahul twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT neffnorma twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT quakestephenr twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT weissmanirvingl twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT voskoboynikayelet twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate AT mannilucia twodistinctevolutionaryconservedneuraldegenerationpathwayscharacterizedinacolonialchordate |