Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate

Author:

Anselmi Chiara12,Kowarsky Mark3ORCID,Gasparini Fabio4,Caicci Federico4,Ishizuka Katherine J.1,Palmeri Karla J.1,Raveh Tal2,Sinha Rahul2,Neff Norma5ORCID,Quake Stephen R.56,Weissman Irving L.257ORCID,Voskoboynik Ayelet1257,Manni Lucia4

Affiliation:

1. Stanford University, Hopkins Marine Station, Pacific Grove, CA 93950

2. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305

3. Department of Physics, Stanford University, Stanford, CA 94305

4. Dipartimento di Biologia, Università degli Studi di Padova, 35131, Padova, Italy

5. Chan Zuckerberg Biohub, San Francisco CA 94158

6. Departments of Applied Physics and Bioengineering, Stanford University, Stanford, CA 94305

7. Department of Biology, Stanford University, Hopkins Marine Station, Pacific Grove, CA 93950

Abstract

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.

Funder

Chan Zuckerberg investigator program

Stinehart Reed Foundation

Progetti di Ricerca di Ateneo, Padova University

Larry L Hillblom foundation Postdoctoral Fellowship

Stanford School of Medicine Dean's Postdoctoral Fellowship

Aldo Gini Foundation Fellowship

Iniziative di Cooperazione Universitaria 2017 Fellowship

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3