Pascal Kaeser

Pascal Kaeser, M.D.

Professor of Neurobiology, Harvard Medical School

Our goal is to understand molecular mechanisms that underlie functions and plasticity of release sites for neurotransmitters and neuromodulators. Neurons predominantly communicate through fast neurotransmission at synapses. Synaptic and neuronal activity levels are tightly controlled, and adjusted to changes in demand. Prominent cellular events that underlie these adaptations are synaptic plasticity and neuromodulation via release of non-classical transmitters. My laboratory is interested in molecular mechanisms at presynaptic neurotransmitter release sites that participate in controlling neuronal activity, and we pursue two missions. (1) It is known that synaptic vesicles containing neurotransmitters fuse exclusively at hot spots for release in presynaptic nerve terminals called active zones. Active zones are fascinating molecular machines that consist of a complex network of multi-domain proteins, orchestrating the ultrafast membrane trafficking process required for synaptic transmission. We are investigating the composition of active zones, how they operate, how they change during plasticity and learning, and how these changes tune behaviors. (2) Neuronal activity is regulated by an intriguing variety of non-classical neurotransmitters called neuromodulators. Prominent neuromodulatory substances include a multitude of neuropeptides, monoamines such as dopamine, and neurotrophins. The machinery that mediates their release, however, is poorly understood. We are dissecting the molecular apparatus that controls release of dopamine, which will reveal general mechanisms of neuromodulation. Understanding dopamine release will also provide a molecular framework to investigate aspects of neuro-psychiatric disorders. Studies in my laboratory are founded on molecular and biochemical methods to identify novel components and protein interactions at neuronal release sites. We employ techniques ranging from conditional gene targeting in mice to electrophysiological and optogenetic analyses of synaptic activity to dissect their roles.

"My laboratory is interested in molecular mechanisms at presynaptic neurotransmitter release sites that participate in controlling neuronal activity."

Publications View
Fusion Competent Synaptic Vesicles Persist upon Active Zone Disruption and Loss of Vesicle Docking.
Authors: Authors: Wang SSH, Held RG, Wong MY, Liu C, Karakhanyan A, Kaeser PS.
Neuron
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ELKS controls the pool of readily releasable vesicles at excitatory synapses through its N-terminal coiled-coil domains.
Authors: Authors: Held RG, Liu C, Kaeser PS.
Elife
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RIM1 and RIM2 redundantly determine Ca2+ channel density and readily releasable pool size at a large hindbrain synapse.
Authors: Authors: Han Y, Babai N, Kaeser P, Südhof TC, Schneggenburger R.
J Neurophysiol
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The active zone protein family ELKS supports Ca2+ influx at nerve terminals of inhibitory hippocampal neurons.
Authors: Authors: Liu C, Bickford LS, Held RG, Nyitrai H, Südhof TC, Kaeser PS.
J Neurosci
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Sensory-related neural activity regulates the structure of vascular networks in the cerebral cortex.
Authors: Authors: Lacoste B, Comin CH, Ben-Zvi A, Kaeser PS, Xu X, Costa Lda F, Gu C.
Neuron
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Molecular mechanisms for synchronous, asynchronous, and spontaneous neurotransmitter release.
Authors: Authors: Kaeser PS, Regehr WG.
Annu Rev Physiol
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Directing traffic into the future.
Authors: Authors: Antonny B, Audhya J, l Bagnat M, von Blume J, Briggs JA, Giraudo C, Kaeser PS, Miller E, Reinisch K, Sbalzarini IF, Schuldiner M, Shen J, Takamori S, Verstreken P, Walther T.
Dev Cell
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RIM genes differentially contribute to organizing presynaptic release sites.
Authors: Authors: Kaeser PS, Deng L, Fan M, Südhof TC.
Proc Natl Acad Sci U S A
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Neurotransmitter release at the thalamocortical synapse instructs barrel formation but not axon patterning in the somatosensory cortex.
Authors: Authors: Narboux-Nême N, Evrard A, Ferezou I, Erzurumlu RS, Kaeser PS, Lainé J, Rossier J, Ropert N, Südhof TC, Gaspar P.
J Neurosci
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Region-specific deletions of RIM1 reproduce a subset of global RIM1a(-/-) phenotypes.
Authors: Authors: Haws ME, Kaeser PS, Jarvis DL, Südhof TC, Powell CM.
Genes Brain Behav
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