RT Journal Article
SR Electronic
T1 Neuronal hemoglobin induces α-synuclein cleavage and loss of dopaminergic neurons
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2021.10.13.464204
DO 10.1101/2021.10.13.464204
A1 Santulli Chiara
A1 Bon Carlotta
A1 De Cecco Elena
A1 Codrich Marta
A1 Narkiewicz Joanna
A1 Parisse Pietro
A1 Perissinotto Fabio
A1 Claudio Santoro
A1 Francesca Persichetti
A1 Legname Giuseppe
A1 Stefano Espinoza
A1 Gustincich Stefano
YR 2021
UL http://biorxiv.org/content/early/2021/10/14/2021.10.13.464204.abstract
AB Backgroud α-synuclein, a protein involved in the pathogenesis of several neurodegenerative disorders, is subjected to several post-translational modifications. Among them, C-terminal truncation seems to increase its aggregation propensity in vitro. Hemoglobin is the major protein in erythrocytes to carries oxygen and recently is found to be expressed in dopaminergic neurons and to be involved in the pathogenesis of neurodegenerative diseases such as Parkinson’s disease.Methods To assess the role of hemoglobin in α-synuclein post-translational modification and in dopamine cells physiology, we over-expressed α and β-chains of Hb in iMN9D dopamine cells to evaluate its effect on α-synuclein truncation. Using an AAV9 we expressed α and β-chains of hemoglobin in dopamine neurons of Substantia Nigra pars compacta and evaluate its effect on α-synuclein post-translational modification, dopamine neurons survivals and behavioural outcome.Results The over-expression of α and β-chains of hemoglobin in iMN9D dopamine cells increased C-terminal truncation of α-synuclein when cells were treated with α-synuclein preformed fibrils. This cleavage was led at least in part by Calpain protease. Hemoglobin over-expression in Substantia Nigra pars compacta induced a similar pattern of α-synuclein truncation and a decrease in tyrosine hydroxylase expression, unveiling a decrease of dopamine neurons of about 50%. This dopamine cells loss led to a mild motor impairment and a deficit in recognition and spatial working memory.Conclusion Our study reveals a novel role for hemoglobin in α-synuclein post-translational modification and in dopamine neurons homeostasis suggesting neuronal hemoglobin is an important modifier in synucleinopathies such as Parkinson’s disease.Competing Interest StatementThe authors have declared no competing interest.α-synalpha-synucleinMsmonomersPTMspost-translational modificationspSer-129phosphorylated serine 129ΔC- α-synC-terminal truncated α-synFL- α-synfull-length α-synPDParkinson’s diseaseLBDLewy Body DementiaMSAMultiple System AtrophySNpcSubtantia nigra pars compactaGCIsGlial cytoplasmic inclusionsDAdopaminergicHbhemoglobinnHbneuronal HbMPP+1-methyl-4-phenylpyridiniumPFFspre-formed fibrilsAFMAtomic force microscopyNHPnon-human primatesCapn ICalpain ICtsdcathepsin DCas1caspase 1THtyrosine hydroxylaseNORnovel object recognition;