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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...

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Autores principales: 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
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
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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.
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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
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