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Group
members:
Joel Jakobsson, postdoc
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LENNART
BRODIN
Department of Neuroscience
Lennart.Brodin@ki.se
Information processing in the brain
depends on release of neurotransmitters from synaptic vesicles at nerve
terminals. We study the molecular mechanisms that control synaptic vesicle
cycling in the developing and adult nervous system, and the relationship
between these mechanisms and neurodegenerative disease mechanisms. Current
problems include how the direct and endosomal routes of synaptic vesicle
recycling are regulated, and how amyloid precursor protein (APP) is
processed into Abeta peptides in nerve terminals. Formation of toxic
Abeta peptides at synapses has been linked with the level of synaptic
vesicle cycling in nerve terminals, and it is thought to contribute
to the synaptic pathology in Alzheimer's disease.
5
SELECTED
PUBLICATIONS:
Brodin L, Gregory J,and Ackermann F.
(2011) Soluble membrane trafficking proteins taking a break at silent
synaptic vesicles. Proc. Natl. Acad. Sci. USA 108, 16869-16870.
Jakobsson J, Ackermann F, Andersson
F, Larhammar D, Löw P, and Brodin L. (2011) Regulation of synaptic
vesicle budding and dynamin function by an EHD ATPase. J. Neurosci.
31, 13972-13980.
Andersson F, Löw P, Brodin L.
(2010) Selective perturbation of the BAR domain of endophilin impairs
synaptic vesicle endocytosis. Synapse 64, 556-560.
Jakobsson, J., Gad, H., Andersson,
F., Löw, P., Shupliakov, O., Brodin, L. (2008) Role of epsin in
synaptic vesicle endocytosis. Proc. Natl. Acad. Sci. USA 10,
6445-6450.
Andersson, F., Jakobsson, J., Löw,
P., Shupliakov, O., Brodin, L. (2008) Perturbation of syndapin/PACSIN
impairs synaptic vesicle endocytosis evoked by intense stimulation.
J. Neurosci. 28, 3925-3933.
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more information, please visit our lab
website.
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