Multiple Forms of Neural Cell Death in the Cyclical Brain Degeneration of A Colonial Chordate

Author:

Anselmi Chiara123,Caicci Federico4ORCID,Bocci Tommaso5ORCID,Guidetti Matteo56ORCID,Priori Alberto5ORCID,Giusti Veronica7,Levy Tom12ORCID,Raveh Tal2,Voskoboynik Ayelet128ORCID,Weissman Irving L.29,Manni Lucia4ORCID

Affiliation:

1. Hopkins Marine Station, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Pacific Grove, CA 93950, USA

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

3. Wu Tsai Neurosciences Institute, Stanford University, Stanford, CA 94305, USA

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

5. “Aldo Ravelli” Center for Neurotechnology and Experimental Brain Therapeutics, Department of Health Sciences, University of Milan, 20142 Milan, Italy

6. Department of Electronics, Information and Bioengineering, Politecnico di Milano, 20133 Milan, Italy

7. San Camillo Hospital srl, IRCCS, 30126 Venezia, Italy

8. Chan Zuckerberg Biohub, San Francisco, CA 94158, USA

9. Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA

Abstract

Human neuronal loss occurs through different cellular mechanisms, mainly studied in vitro. Here, we characterized neuronal death in B. schlosseri, a marine colonial tunicate that shares substantial genomic homology with mammals and has a life history in which controlled neurodegeneration happens simultaneously in the brains of adult zooids during a cyclical phase named takeover. Using an ultrastructural and transcriptomic approach, we described neuronal death forms in adult zooids before and during the takeover phase while comparing adult zooids in takeover with their buds where brains are refining their structure. At takeover, we found in neurons clear morphologic signs of apoptosis (i.e., chromatin condensation, lobed nuclei), necrosis (swollen cytoplasm) and autophagy (autophagosomes, autolysosomes and degradative multilamellar bodies). These results were confirmed by transcriptomic analyses that highlighted the specific genes involved in these cell death pathways. Moreover, the presence of tubulovesicular structures in the brain medulla alongside the over-expression of prion disease genes in late cycle suggested a cell-to-cell, prion-like propagation recalling the conformational disorders typical of some human neurodegenerative diseases. We suggest that improved understanding of how neuronal alterations are regulated in the repeated degeneration–regeneration program of B. schlosseri may yield mechanistic insights relevant to the study of human neurodegenerative diseases.

Funder

NIH

Chan Zuckerberg Investigator Program

Stinehart-Reed

University of Padova

Gruss Lipper Postdoctoral Fellowship

Larry L. Hillblom Foundation Postdoctoral Fellowship

Knight Initiative for Brain Resilience Scholar Award

Wu Tsai Neurosciences Institute

Stanford University

Publisher

MDPI AG

Subject

General Medicine

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