The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity

Valeria Crippa, Maria Elena Cicardi, Nandini Ramesh, Samuel J. Seguin, Massimo Ganassi, Ilaria Bigi, Chiara Diacci, Elena Zelotti, Madina Baratashvili, Jenna Gregory, Christopher M. Dobson, Cristina Cereda, Udai Bhan Pandey, Angelo Poletti, Serena Carra

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70 Citations (Scopus)


Aggregation of TAR-DNA-binding protein 43 (TDP-43) and of its fragments TDP-25 and TDP-35 occurs in amyotrophic lateral sclerosis (ALS). TDP-25 and TDP-35 act as seeds for TDP-43 aggregation, altering its function and exerting toxicity. Thus, inhibition of TDP-25 and TDP-35 aggregation and promotion of their degradation may protect against cellular damage. Upregulation of HSPB8 is one possible approach for this purpose, since this chaperone promotes the clearance of an ALS associated fragments of TDP-43 and is upregulated in the surviving motor neurones of transgenic ALS mice and human patients. We report that overexpression of HSPB8 in immortalized motor neurones decreased the accumulation of TDP-25 and TDP-35 and that protection against mislocalized/truncated TDP-43 was observed for HSPB8 in Drosophila melanogaster. Overexpression of HSP67Bc, the functional ortholog of human HSPB8, suppressed the eye degeneration caused by the cytoplasmic accumulation of a TDP-43 variant with a mutation in the nuclear localization signal (TDP-43-NLS). TDP-43-NLS accumulation in retinal cells was counteracted by HSP67Bc overexpression. According with this finding, downregulation of HSP67Bc increased eye degeneration, an effect that is consistent with the accumulation of high molecular weight TDP-43 species and ubiquitinated proteins. Moreover, we report a novel Drosophila model expressing TDP-35, and show that while TDP-43 and TDP-25 expression in the fly eyes causes a mild degeneration, TDP-35 expression leads to severe neurodegeneration as revealed by pupae lethality; the latter effect could be rescued by HSP67Bc overexpression. Collectively, our data demonstrate that HSPB8 upregulation mitigates TDP-43 fragment mediated toxicity, in mammalian neuronal cells and flies.
Original languageEnglish
Pages (from-to)3908-3924
JournalHuman Molecular Genetics
Issue number18
Publication statusPublished - 15 Sept 2016

Bibliographical note

We thank Dr. JP Taylor for providing the fly lines expressing WT or mutant NLS TDP-43 used in this study. We thank Prof. L Petrucelli for providing the GFP-TDPs plasmids and Dr. E Garattini for providing the TR4 NSC34 cell line. We are grateful to Dr. Leila Luheshi for advice and valuable discussions. We thank Dr. Harm H. Kampinga for fruitful discussion and for providing the transgenic flies expressing V5-HSP67Bc.


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