Michel De Waard

Prof. Michel De Waard

Inserm
+2
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 March 1994 in Nature
Verified
Journal Article
Closed access
PDF file
MPMarion Pragnell
Marion Pragnell
Michel De WaardMichel De Waard
Michel De Waard
YMYasuo Mori
Yasuo Mori
TTTsutomu Tanabe
Tsutomu Tanabe
TSTerry P. Snutch
Terry P. Snutch
KCKevin Campbell
Kevin Campbell

1 May 2000 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
AEAndrew Escayg
Andrew Escayg
Michel De WaardMichel De Waard
Michel De Waard
DLDavid D. Lee
David D. Lee
DBDelphine Bichet
Delphine Bichet
PWPeter Wolf
Peter Wolf
MMMiriam H. Meisler
Miriam H. Meisler

1 January 2000 in Neuron
Verified
Journal Article
Closed access
DBDelphine Bichet
Delphine Bichet
VCVéronique Cornet
Véronique Cornet
SGSandrine Geib
Sandrine Geib
ECEdmond Carlier
Edmond Carlier
SVStephen Volsen
Stephen Volsen
Michel De WaardMichel De Waard
Michel De Waard

1 April 1998 in Trends in Neurosciences
Verified
Journal Article
Closed access
DWDenise Walker
Denise Walker
Michel De WaardMichel De Waard
Michel De Waard


13 May 2007 in Nature Neuroscience
Verified
Journal Article
Open access
PDF file
SKShigeki Kiyonaka
Shigeki Kiyonaka
MWMinoru Wakamori
Minoru Wakamori
TMTakafumi Miki
Takafumi Miki
YUYoshitsugu Uriu
Yoshitsugu Uriu
MNMio Nonaka
Mio Nonaka
YMYasuo Mori
Yasuo Mori
The molecular organization of presynaptic active zones is important for the neurotransmitter release that is triggered by depolarization-induced Ca2+ influx. Here, we demonstrate a previously unknown interaction between two components of the presynaptic active zone, RIM1 and voltage-dependent Ca2+ channels (VDCCs), that controls neurotransmitter release in mammalian neurons. RIM1 associated with VDCC β-subunits via its C terminus to markedly suppress voltage-dependent inactivation among different neuronal VDCCs. Consistently, in pheochromocytoma neuroendocrine PC12 cells, acetylcholine release was significantly potentiated by the full-length and C-terminal RIM1 constructs, but membrane docking of vesicles was enhanced only by the full-length RIM1. The β construct beta-AID dominant negative, which disrupts the RIM1-β association, accelerated the inactivation of native VDCC currents, suppressed vesicle docking and acetylcholine release in PC12 cells, and inhibited glutamate release in cultured cerebellar neurons. Thus, RIM1 association with β in the presynaptic active zone supports release via two distinct mechanisms: sustaining Ca2+ influx through inhibition of channel inactivation, and anchoring neurotransmitter-containing vesicles in the vicinity of VDCCs.