INSERM U1242 Oncogenesis Stress Signaling - SPECIAL SEMINAR
Dr Julien VILLENEUVE - Institute of Functional Genomics (IGF) MONTPELLIER : "Mechanisms of Unconventional Protein Secretion – from basic research to neurodegenerative disease therapeutics"
Dienstag 15 Dezember, 11:00
200
Mechanisms of Unconventional Protein Secretion – from basic research to neurodegenerative disease therapeutics
Dr. Julien VILLENEUVE
CRCN at CNRS
Institute of Functional Genomics (IGF) - MONTPELLIER
Abstract
Alzheimer's and Parkinson's diseases are neurodegenerative diseases (NDs), characterized by the accumulation of misfolded and aggregated proteins such as Tau and alpha-synuclein (aSNC) in the central nervous system. These pathogenic proteins can spread from cell to cell, and this intercellular propagation contributes to the disease progression. Therefore, uncovering the molecular and cellular mechanisms underlying the intercellular transmission of Tau and aSNC is of utmost importance.
Recently, we demonstrated that lysosomes can play a critical role in the unconventional secretion of Tau and aSNC through lysosomal exocytosis. Thus, a critical challenge now is to understand what makes lysosomes a transport carrier and secretory compartment, promoting Tau and αSNC dissemination.
Toward this objective, we are dissecting the molecular determinants required to divert lysosomes toward compartments competent for fusion with the plasma membrane, and to identify factors involved at every step of Tau and αSNC trafficking. For this, functional assays on lysosomes, pooled genome-wide CRISPR screens, and proteomic approaches are used. Second, we are investigating the role of identified factors in iPSC-derived neurons and zebrafish and drosophila models to validate their pathological relevance and reveal their therapeutic potential. Finally, we are testing the role of lysosomes as the main sorting station in ND patients by assessing the levels of lysosomal enzymes in cerebrospinal fluid (CSF) of patients.
Overall, our work may lead to the identification of novel therapeutic targets and diagnostic markers, paving the way for innovative strategies to prevent or slow the progression of NDs.
INSERM U1242 Oncogenesis Stress Signaling - SPECIAL SEMINAR
Dr Julien VILLENEUVE - Institute of Functional Genomics (IGF) MONTPELLIER : "Mechanisms of Unconventional Protein Secretion – from basic research to neurodegenerative disease therapeutics"
Dienstag 15 Dezember, 11:00
200
Mechanisms of Unconventional Protein Secretion – from basic research to neurodegenerative disease therapeutics
Dr. Julien VILLENEUVE
CRCN at CNRS
Institute of Functional Genomics (IGF) - MONTPELLIER
Abstract
Alzheimer's and Parkinson's diseases are neurodegenerative diseases (NDs), characterized by the accumulation of misfolded and aggregated proteins such as Tau and alpha-synuclein (aSNC) in the central nervous system. These pathogenic proteins can spread from cell to cell, and this intercellular propagation contributes to the disease progression. Therefore, uncovering the molecular and cellular mechanisms underlying the intercellular transmission of Tau and aSNC is of utmost importance.
Recently, we demonstrated that lysosomes can play a critical role in the unconventional secretion of Tau and aSNC through lysosomal exocytosis. Thus, a critical challenge now is to understand what makes lysosomes a transport carrier and secretory compartment, promoting Tau and αSNC dissemination.
Toward this objective, we are dissecting the molecular determinants required to divert lysosomes toward compartments competent for fusion with the plasma membrane, and to identify factors involved at every step of Tau and αSNC trafficking. For this, functional assays on lysosomes, pooled genome-wide CRISPR screens, and proteomic approaches are used. Second, we are investigating the role of identified factors in iPSC-derived neurons and zebrafish and drosophila models to validate their pathological relevance and reveal their therapeutic potential. Finally, we are testing the role of lysosomes as the main sorting station in ND patients by assessing the levels of lysosomal enzymes in cerebrospinal fluid (CSF) of patients.
Overall, our work may lead to the identification of novel therapeutic targets and diagnostic markers, paving the way for innovative strategies to prevent or slow the progression of NDs.
