Graduate Studies Faculty
Henrique P. von Gersdorff, Ph.D.
Programs:Cell & Developmental Biology
Neuroscience Graduate Program
Program in Molecular & Cellular Biosciences
Research Interests:exocytosis and endocytosis of synaptic vesicles, short and long-term plasticity in the retina and brainstem, electrophysiology of auditory pathway, systems » Click here for more about Dr. von Gersdorff's research » PubMed Listing
Preceptor RotationsDr. von Gersdorff has not indicated availability for preceptor rotations at this time.
Faculty MentorshipDr. von Gersdorff has not indicated availability as a mentor at this time.
Henrique von Gersdorff earned a Ph.D. in Physics from the University of Minnesota and a Ph.D. in Neurobiology from Stony Brook University in New York. He received his B.S. in Physics from the Federal University of Rio de Janeiro, Brazil. He was a research scientist in high-energy physics at Brookhaven National Laboratory, and had postdoctoral fellowships at Stony Brook University and the Max-Planck Institute for Biophysical Chemistry, Department of Membrane Biophysics, Göttingen. In 1998 he was appointed assistant scientist in the Vollum Institute and was promoted to scientist in 2004 and senior scientist in 2009. vonGersdorff also holds a faculty appointment in the Physiology and Pharmacology department of OHSU.
Summary of Current Research
Sensory information is conveyed by neurons and synapses specialized to faithfully transmit large amounts of information at high rates. A key event in synaptic transmission is the release of neurotransmitter via vesicle fusion at synaptic terminals. Direct studies of synaptic terminals have been hampered by their small sizes and technical constraints. However, using high time resolution patch-clamp membrane capacitance measurements, von Gersdorff and his associates have studied the kinetics of vesicle fusion (exocytosis) and subsequent membrane retrieval (endocytosis) in single, live synaptic terminals from bipolar cells of the goldfish retina and from hair cells of the frog amphibian papilla. These cells have compact ribbon-type active zones that contain a large pool of releasable vesicles suitable for the transfer of high bandwidths of information. Following short depolarizations, a fast form of endocytosis can be observed, indicating that synaptic vesicle membrane is quickly re-internalized after vesicle fusion. Von Gersdorff and his colleagues are presently investigating mechanisms for short-term synaptic plasticity at ribbon synapses in mouse retinal slices and also multivesicular release at the hair cell synapses using capacitance measurements together with paired recordings of hair cells and their afferent fibers. The lab is also using imaging techniques to record optically the fast dynamics of calcium changes in active zones and nerve fibers.
To study conventional active zone synapses, the lab has been examining the calyx of Held nerve terminal, a pivotal element in the auditory brainstem circuitry that computes sound source localization. Precise timing of action potential discharges is essential for accomplishing this task. Nevertheless, the mechanisms that modulate and preserve the timing of spikes are poorly understood. Von Gersdorff and his coworkers are studying these mechanisms and short-term forms of plasticity at this synapse. The large size of the calyx terminal allows them to directly patch-clamp the terminal and the postsynaptic cell simultaneously, and thus to measure calcium currents, presynaptic capacitance changes, and glutamate release. This direct access to the terminal allows the lab to study the kinetics of synaptic vesicle exocytosis and endocytosis, neurotransmitter reuptake mechanisms, and the modulation of postsynaptic spikes. Presently, the lab is focused on revealing the developmental changes that fine-tune auditory synapses for short synaptic delays and for sustained high frequency firing.
Kim MH, von Gersdorff H. (2016) Postsynaptic plasticity triggered by Ca2+-permeable AMPA receptor activation in retinal amacrine cells. Neuron 89:507-520.
Delvendahl I, Vyleta NP, von Gersdorff H, Hallermann S. (2016) Fast, temperature-sensitive and clathrin-independent endocytosis at central synapses. Neuron 90:492-498.
Balakrishnan V, Puthussery T, Kim MH, Taylor WR, von Gersdorff H. (2015) Synaptic vesicle exocytosis at the dendritic lobules of an inhibitory interneuron in the mammalian retina. Neuron 87:563-575.
Cho S, von Gersdorff H. (2014) Proton-mediated block of Ca2+ channels during multivesicular release regulates short-term plasticity at an auditory hair cell synapse. J. Neurosci. 34:15877-15887.
Li GL, Cho S, von Gersdorff H. (2014) Phase-locking precision is enhanced by multiquantal release at an auditory hair cell ribbon synapse. Neuron 83:1404-1417.
Portfors CV, von Gersdorff H (2013) Macrocircuits for sound localization use leaky coincidence detectors and specialized synapses. Neuron 78:755-757.
Kim JH, Renden R, von Gersdorff H. (2013) Dysmyelination of auditory afferent axons increases the jitter of action potential timing during high-frequency firing. J. Neurosci. 33:9402-9407.
Kim MH, Li GL, von Gersdorff H. (2013) Single Ca2+ channels and exocytosis at sensory synapses. J. Physiol. 591:3167-3178.
Vickers E, Kim MH, Vigh J, von Gersdorff H. (2012) Paired-pulse plasticity in the strength and latency of light-evoked lateral inhibition to retinal bipolar cell terminals. J. Neurosci. 32:11688-11699.
Graydon CW, Cho S, Li GL, Kachar B, von Gersdorff H. (2011) Sharp Ca2+ nanodomains beneath the ribbon promote highly synchronous multivesicular release at hair cell synapses. J. Neurosci. 31:16637-16650.
Vigh J, Vickers E, von Gersdorff H. (2011) Light-evoked lateral GABAergic inhibition at single bipolar cell synaptic terminals is driven by distinct retinal microcircuits. J. Neurosci. 31:15884-15893.
Cho S, Li GL, von Gersdorff H. (2011) Recovery from short-term depression and facilitation is ultrafast and Ca2+ dependent at auditory hair cell synapses. J. Neurosci. 31:5682-5692.
Kim JH, Kushmerick C, von Gersdorff H. (2010) Presynaptic resurgent Na+ currents sculpt the action potential waveform and increase firing reliability at a CNS nerve terminal. J. Neurosci. 30:15479-15490.