Neural Microcircuits
The Retinal Microcircuits Laboratory is interested in the cellular and molecular basis of synaptic transmission and synaptic integration in the central nervous system. Our main goal is to understand and characterize the synaptic and cellular mechanisms employed by identified neurons and specific microcircuits for signal processing.
About the research group
Our lab is interested in the cellular and molecular basis of synaptic transmission and synaptic integration in the central nervous system. Our main goal is to understand and characterize the synaptic and cellular mechanisms employed by identified neurons and specific microcircuits for signal processing. The primary technique is that of targeted patch-clamp recording of visually-identified neurons using voltage clamp, current clamp and dynamic clamp recording configurations. This electrophysiological work is currently performed using an in vitro slice preparation of the rat retina, a preparation that offers the possibility to combine modern electrophysiological techniques with the use of natural stimuli to activate specific neuronal circuits.
Neural Microcircuits is part of the Basic and Translational Neuroscience research unit at the Department of Biomedicine.
Projects
Current projects include
- Performing combined multi-photon excitation imaging and patch-clamp recording to study healthy tissue and processes of neurodegeneration
- Performing Ca2+-imaging in retinal slices
- Performing quantitative morphological reconstructions of single neurons by computer-aided manual tracing of image stacks acquired with multi-photon excitation microscopy
- Constructing compartmental models of single neurons to study passive and active properties involved in signal processing
- Performing simultaneous multi-electrode recordings from neurons in specific microcircuits within the inner retina
- Studying the location and functional properties of NMDA receptors in retinal microcircuits
- Utilizing dynamic clamp to artificially insert synapses and conductances into neurons, enabling us to study the mechanisms underlying the dynamic properties of neurons and microcircuits.
- Performing confocal and STED microscopy to localize receptors and synaptic proteins to individual neurons
Publications
Recent Publications
Hartveit E, Veruki ML (2025). Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices. Bio-Protocol 15(1):e5147. doi: 10.21769/BioProtoc.5147.
Beltrán-Matas P, Hartveit E, Veruki ML (2023). Functional properties of GABAA receptors of AII amacrine cells of the rat retina. Frontiers in Ophthalmology 3 DOI=10.3389/fopht.2023.1134765 (Open access).
Liu JH, Peter DO, Guttormsen MSF, Hossain Md K, Gerking Y, Veruki ML, Hartveit E (2022). The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution. Visual Neuroscience 39:E004 doi.org/10.1017/S0952523822000025 (Open access).
Beltrán-Matas P, Castilho Á, Tencer B, Veruki ML*, Hartveit E* (2022). Inhibitory inputs to an inhibitory interneuron: Spontaneous postsynaptic currents and GABA A receptors of A17 amacrine cells in the rat retina. European Journal of Neuroscience 55: 1442-1470 (*corresponding authors; Open access).
Hartveit E, Veruki ML, Zandt BJ (2022). Dendritic morphology of an inhibitory retinal interneuron enables simultaneous local and global synaptic integration. Journal of Neuroscience 42: 1630-1647.
Fournel R, Veruki ML, Hartveit E (2022). Digital reconstruction and quantitative morphometric analysis of bipolar cells in live rat retinal slices. Journal of Comparative Neurology doi: 10.1002/cne.25308. (Open access)
Liu JH, Singh JB, Veruki ML, Hartveit E (2021). Morphological properties of the axon initial segment-like process of AII amacrine cells in the rat retina. The Journal of Comparative Neurology doi: 10.1002/cne.25210. (Open access)
Beltrán-Matas P, Hartveit E, Veruki ML (2021). Different glutamate sources and endogenous co-agonists activate extrasynaptic NMDA receptors on amacrine cells of the rod pathway microcircuit. European Journal of Neuroscience doi: 10.1111/ejn.15325. (Open access)
Fournel R, Hartveit E, Veruki ML (2020). Differential contribution of gap junctions to the membrane properties of ON- and OFF-bipolar cells of the rat retina. Cellular and Molecular Neurobiology (Open access: https://doi.org/10.1007/s10571-020-00845-y)
Hartveit E, Veruki ML, Zandt BJ (2019). Capacitance measurement of dendritic exocytosis in an electrically coupled inhibitory retinal interneuron: an experimental and computational study. Physiological Reports 7:e14186. doi: 10.14814/phy2.14186. (PDF)
Veruki ML, Zhou Y, Castilho Á, Morgans CW, Hartveit E (2019). Extrasynaptic NMDA Receptors on Rod Pathway Amacrine Cells: Molecular Composition, Activation, and Signaling. Journal of Neuroscience 2019 Jan 23;39:627-650.
Zandt BJ, Veruki ML, Hartveit E. (2018). Electrotonic signal processing in AII amacrine cells: compartmental models and passive membrane properties for a gap junction-coupled retinal neuron. Brain Structure and Function doi: 10.1007/s00429-018-1696-z.
Veruki ML & Schubert T. (2018) Neural Circuits: When Neurons 'Remember' Their Connectivity. Current Biology 28(11):R662-R664. doi: 10.1016/j.cub.2018.04.059.
Hartveit E, Zandt BJ, Madsen E, Castilho Á, Mørkve SH, Veruki ML. AMPA receptors at ribbon synapses in the mammalian retina: kinetic models and molecular identity. Brain Structure and Function 223(2):769-804. 2018 Mar;223(2):769-804.
Zandt BJ, Losnegård A, Hodneland E, Veruki ML, Lundervold A, Hartveit E. (2017). Semi-automatic 3D morphological reconstruction of neurons with densely branching morphology: Application to retinal AII amacrine cells imaged with multi-photon excitation microscopy. Journal of Neuroscience Methods 279:101-118.
Zandt BJ, Liu JH, Veruki ML, Hartveit E. (2017). AII amacrine cells: quantitative reconstruction and morphometric analysis of electrophysiologically identified cells in live rat retinal slices imaged with multi-photon excitation microscopy. Brain Structure and Function 222(1):151-182.
Zhou Y, Tencerová B, Hartveit E, Veruki ML. (2016). Functional NMDA receptors are expressed by both AII and A17 amacrine cells in the rod pathway of the mammalian retina. Journal of Neurophysiology 115:389-403.
Castilho Á, Madsen E, Ambrósio AF, Veruki ML, Hartveit E (2015). Diabetic hyperglycemia reduces Ca2+ permeability of extrasynaptic AMPA receptors in AII amacrine cells. Journal of Neurophysiology 114: 1545-53.
Castilho Á, Ambrósio AF, Hartveit E, Veruki ML (2015).Disruption of a neural microcircuit in the rod pathway of the mammalian retina by diabetes mellitus. Journal of Neuroscience 35: 5422-33.
Hartveit E & Veruki ML (2012). Electrical synapses between AII amacrine cells in the retina: Function and modulation. Brain Research. 1487:160-72.
Books
Multiphoton Microscopy (2019) edited by Espen Hartveit. Springer Nature, Neuromethods Series, ISBN 978-1-4939-9702-2
Highlighted Publications
Hartveit E, Veruki ML, Zandt BJ (2022). Dendritic morphology of an inhibitory retinal interneuron enables simultaneous local and global synaptic integration. Journal of Neuroscience 42: 1630-1647.
Veruki ML, Zhou Y, Castilho Á, Morgans CW, Hartveit E (2019). Extrasynaptic NMDA Receptors on Rod Pathway Amacrine Cells: Molecular Composition, Activation, and Signaling. Journal of Neuroscience 2019 Jan 23;39:627-650.
Wang X, Veruki ML, Bukoreshtliev NV, Hartveit E, Gerdes HH (2010). Animal cells connected by nanotubes can be electrically coupled through interposed gap-junction channels. Proceedings of the National Academy of Sciences U S A. 107: 17194-9.
Castilho Á, Ambrósio AF, Hartveit E, Veruki ML (2015).Disruption of a neural microcircuit in the rod pathway of the mammalian retina by diabetes mellitus. Journal of Neuroscience 35: 5422-33.
Hartveit E & Veruki ML (2007). Studying properties of neurotransmitter receptors by non-stationary noise analysis of spontaneous postsynaptic currents and agonist-evoked responses in outside-out patches. Nature Protocols 2: 434-48.
Veruki ML, Mørkve SH & Hartveit E (2006). Activation of a presynaptic glutamate transporter regulates synaptic transmission through electrical signalling. Nature Neuroscience 9: 1388-1396.
Veruki ML & Hartveit E (2002). Electrical synapses mediate signal transmission in the rod pathway of the mammalian retina. Journal of Neuroscience 22: 10558-10566.
Veruki ML & Hartveit E (2002). AII (rod) amacrine cells form a network of electrically coupled interneurons in the mammalian retina. Neuron 33: 935-946.
People
Group manager
Espen Hartveit Professor
Meg Veruki Professor
Group members
Matteo Stefano Luppi PhD candidate
Elaine Elizabeth Orendorff Postdoctoral Fellow
Aurea Castilho Head Engineer
Amanda Louisa Johnsen-Hernandez Master Student
Contact
Are you interested in our research, or do you have any questions? Please contact the research group manager, professor Espen Hartveit.
- Phone number
- +47 55586074
- Emails
- espen.hartveit@uib.no