Aleksandra Pidde
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Aleksandra Pidde has a total of 24 co-authors. Here are the top co-authors by number of shared publications:
- Michael Krieg
ICFO - Institut de Ciències Fotòniques, Castelldefels, The Barcelona Institute of Science and Technology, Barcelona, Spain
3 shared publications - Nawaphat Malaiwong
Institut de Ciencies Fotoniques, Castelldefels, SPAIN
2 shared publications - Neus Sanfeliu-Cerdán
ICFO—Institut de Ciències Fotòniques, Castelldefels, The Barcelona Institute of Science and Technology, Barcelona, Spain
2 shared publications - Ravi Das
Neuroscience Institute, Georgia State University, Atlanta, GA 30303, USA
2 shared publications - Adriana Carolina Gonzalez
Institut de Ciencies Fotoniques, Castelldefels, SPAIN
1 shared publication - Aneta Stefanovska
Physics Department, Lancaster University, Lancaster, UK
1 shared publication
Latest Publications
- 6 April 2023
- Published by Springer Nature in Nature Methods
- Vol. 20 (5) , 761-769
Neural engineering with photons as synaptic transmitters
Neuronal computation is achieved through connections of individual neurons into a larger network. To expand the repertoire of endogenous cellular communication, we developed a synthetic, photon-assisted synaptic transmission (PhAST) system. PhAST is based on luciferases and channelrhodopsins that enable the transmission of a neuronal state across space, using photons as neurotransmitters. PhAST overcomes synaptic barriers and rescues the behavioral deficit of a glutamate mutant with conditional, calcium-triggered photon emission between two neurons of the Caenorhabditis elegans nociceptive avoidance circuit. To demonstrate versatility and flexibility, we generated de novo synaptic transmission between two unconnected cells in a sexually dimorphic neuronal circuit, suppressed endogenous nocifensive response through activation of an anion channelrhodopsin and switched attractive to aversive behavior in an olfactory circuit. Finally, we applied PhAST to dissect the calcium dynamics of the temporal pattern generator in a motor circuit for ovipositioning. In summary, we established photon-based synaptic transmission that facilitates the modification of animal behavior.
- 6 April 2023
- Published by Springer Nature in Nature Methods
- Vol. 20 (5) , 761-769
Neural engineering with photons as synaptic transmitters
Neuronal computation is achieved through connections of individual neurons into a larger network. To expand the repertoire of endogenous cellular communication, we developed a synthetic, photon-assisted synaptic transmission (PhAST) system. PhAST is based on luciferases and channelrhodopsins that enable the transmission of a neuronal state across space, using photons as neurotransmitters. PhAST overcomes synaptic barriers and rescues the behavioral deficit of a glutamate mutant with conditional, calcium-triggered photon emission between two neurons of the Caenorhabditis elegans nociceptive avoidance circuit. To demonstrate versatility and flexibility, we generated de novo synaptic transmission between two unconnected cells in a sexually dimorphic neuronal circuit, suppressed endogenous nocifensive response through activation of an anion channelrhodopsin and switched attractive to aversive behavior in an olfactory circuit. Finally, we applied PhAST to dissect the calcium dynamics of the temporal pattern generator in a motor circuit for ovipositioning. In summary, we established photon-based synaptic transmission that facilitates the modification of animal behavior.
- 7 June 2022
- Published by Elsevier in Current Opinion in Neurobiology
- Vol. 75, 102574
Mechanosensitive body–brain interactions in Caenorhabditis elegans
- 7 June 2022
- Published by Elsevier in Current Opinion in Neurobiology
- Vol. 75, 102574
Mechanosensitive body–brain interactions in Caenorhabditis elegans
- Open Access
- 17 September 2021
- Published by American Association for the Advancement of Science (AAAS) in Science Advances
- Vol. 7 (38)
An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity
Functional compartmentalization of sensory axons by mechanical compression and extension tunes neuronal activity in C. elegans .
- 17 September 2021
- Published by American Association for the Advancement of Science (AAAS) in Science Advances
- Vol. 7 (38)
Open AccessAn asymmetric mechanical code ciphers curvature-dependent proprioceptor activity
Functional compartmentalization of sensory axons by mechanical compression and extension tunes neuronal activity in C. elegans .
- Open Access
- 1 July 2018
- Published by Elsevier in Physics Reports
- Vol. 748, 1-60
Surrogate data for hypothesis testing of physical systems
- 1 July 2018
- Published by Elsevier in Physics Reports
- Vol. 748, 1-60
Open AccessSurrogate data for hypothesis testing of physical systems
- Open Access
- 15 March 2018
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 115 (13) , E3017-E3025
Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
Significance: Networks of neurons need to reliably encode and replay patterns and sequences of activity. In the brain, sequences of spatially coding neurons are replayed in both the forward and reverse direction in time with respect to their order in recent experience. As of yet there is no network-level or biophysical mechanism known that can produce both modes of replay within the same network. Here we propose that resonance, a property of neurons, paired with subthreshold oscillations in neural input facilitate network-level learning of fixed and sequential activity patterns and lead to both forward and reverse replay.
- 15 March 2018
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 115 (13) , E3017-E3025
Open AccessResonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
Significance: Networks of neurons need to reliably encode and replay patterns and sequences of activity. In the brain, sequences of spatially coding neurons are replayed in both the forward and reverse direction in time with respect to their order in recent experience. As of yet there is no network-level or biophysical mechanism known that can produce both modes of replay within the same network. Here we propose that resonance, a property of neurons, paired with subthreshold oscillations in neural input facilitate network-level learning of fixed and sequential activity patterns and lead to both forward and reverse replay.