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

被引:3
作者
Anselmi, Chiara [1 ,2 ,3 ]
Caicci, Federico [4 ]
Bocci, Tommaso [5 ]
Guidetti, Matteo [5 ,6 ]
Priori, Alberto [5 ]
Giusti, Veronica [7 ]
Levy, Tom [1 ,2 ]
Raveh, Tal [2 ]
Voskoboynik, Ayelet [1 ,2 ,8 ]
Weissman, Irving L. L. [2 ,9 ]
Manni, Lucia [3 ,4 ]
机构
[1] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Hopkins Marine Stn, Pacific Grove, CA 93950 USA
[2] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[3] Stanford Univ, Wu Tsai Neurosci Inst, Stanford, CA 94305 USA
[4] Univ Padua, Dipartimento Biol, I-35131 Padua, Italy
[5] Univ Milan, Aldo Ravelli Ctr Neurotechnol & Expt Brain Therape, Dept Hlth Sci, I-20142 Milan, Italy
[6] Politecn Milan, Dept Elect Informat & Bioengn, I-20133 Milan, Italy
[7] IRCCS, San Camillo Hosp Srl, I-30126 Venice, Italy
[8] Chan Zuckerberg Biohub, San Francisco, CA 94158 USA
[9] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
关键词
apoptosis; autophagy; colonial chordate; lysosomal cell death; necroptosis; ASCIDIAN BOTRYLLUS-SCHLOSSERI; AMYLOID PRECURSOR PROTEIN; BLASTOGENETIC CYCLE; NATURAL APOPTOSIS; ALPHA-SYNUCLEIN; GENE-EXPRESSION; NERVOUS-SYSTEM; LIFE-CYCLE; GENERATION; TUNICATA;
D O I
10.3390/cells12071041
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:26
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