Alumni Research Groups
Group Leader: Bert Sakmann, Ph.D.
Research of the Digital Neuroanatomy group at MPFI focused on functional anatomy of circuits in the brain – specifically the cerebral cortex – that form the basis of simple behaviors (e.g. decision making). This research involves the use of large scale, high resolution microscopic techniques to reconstruct individual morphologies, distributions and synaptic wiring of different neuron types. Neurons are recorded from using in vivo and in vitro electrophysiological techniques. The results are used to simulate signal flow in an anatomically realistic network model. Eventually, this may reveal parts of the network that trigger sensory initiated behavior and lead to new discoveries about the brain’s process of learning.
The research group also conducted a program dedicated to obtaining a three-dimensional map of the normal rodent brain. Different neuron types are labeled with specific fluorescent markers. Next, imaging and quantification of neuron distributions is achieved by 3D confocal mosaic microscopy and custom designed automated neuron detection software. This work will provide insight into functional architecture of entire cortical areas, and will thus lay the foundation for future studies on brain degenerative diseases, such as Alzheimer’s.
Molecular Mechanisms of Synaptic Function
Group Leader: Samuel Young, Jr., Ph.D.
The goal of the Molecular Mechanisms of Synaptic Function research group at MPFI was to understand the mechanisms of synaptic vesicle release and recovery that permit the accurate encoding of sound over wide dynamic ranges over varying times scales. The calyx of Held/MNTB synapse in the auditory brainstem is a key connection in this pathway since it provides precise timing and activates sustained inhibition to key binaural cell groups. Its large size has made it an experimentally accessible entry point into understanding the mechanisms and function of these synaptic connections. The calyx can be driven by sound at high rates, operates in the background of varying spontaneous firing rates, and yet must be relatively immune to acoustically noisy backgrounds. How is this achieved? Since the presynapse has a finite supply of fusion competent synaptic vesicles (SVs), termed the readily releasable pool (RRP), the release and replenishment of the RRP must be balanced to sustain transmission. Priming, the creation of fusion competent SVs at the active zone (AZ) that can be released in response to action potentials (APs), is a key regulatory pathway that regulates the RRP release and replenishment to sustain transmitter release. Ultimately, the molecular mechanisms that regulate priming underlie efficient release and replenishment of SVs underpins sound encoding. Therefore, the group aims to define the molecular mechanisms that ensure availability of release competent SVs throughout a wide range of AP firing rates to support the early stages of auditory processing. As release and replenishment of the RRP is necessary in all synapses to encode information over varying timescales, our data will have broad relevance to understanding how synaptic communication leads to information transfer in neural networks.