Prof. Dr. Jochen Staiger
Prof. Dr. Bernhard Reuss
Gabriele Schmidt
Dr. rer. nat. Julien Guy
Dr. rer. nat. Martin Möck
Dr. med. Rebeka Andrea Palicz
Dr. Stefan Pommer
Dr. rer. nat. Joachim Rosenbusch
Dr. rer. nat. Mirko Witte
Merve Özgür Erat
Aybeniz Ece Cetin
Xiaoyi Mao
Felix Preuss
Jenifer Rachel
Harun Akkoyun
Felicita Fischer
Philipp Kolligs
Lukas Müller
Flore Schork
Sophia Heidenreich
Ima Mansori
Leander Matthes
Paul Molis
Sandra Heinzl
Sabrina Hübner
Patricia Sprysch
Pavel Truschow
Dr. rer. nat. Csaba Dávid
Dr. rer. nat. Alvar Prönneke
PD Dr. Michael Rickmann
Dr. Marcel Ruiz Mejias
Dr. rer. nat. Dirk Schubert
Dr. Godwin Sokpor
Dr. rer. nat. Nidhi Subhashini
Dr. rer. nat. Tran Tuoc
Dr. med. Robin Wagener
Dr. rer. nat. Yuanbin Xie
Dr. rer. nat. Xiaojuan Zhou
Eman Abbas
Weilin Chen
Michael Feyerabend
Georg Hafner
Kamila Kiszka
Anouk Meeuwissen
Nieves Mingo Moreno
Ramanathan Narayanan
Huong Nguyen
Pauline Antonie Ulmke
Florian Walker
Khatuna Aslanishvili
Christina Bachmann
Simon Badura
Thore Behrendt
Jürgen Delchmann
Esther Alexandra Dockhorn
Tatjana Fischer
Anna Garcia Galera
Kristina Glöckner
Janis Hülsemann
Dilbrin Khelo
Stephen Olt
Bettina Pater
Alina Rüppel
Alexandra Sachkova
Bianca Scheuer
Lisa Thiecke
Joris Brehmer
Dennis Dalügge
Julia Dziubek
Ricardo Castro Hernandez
Fernando Gonzalez Ibanez
Christin Korb
Anette Mertens
Megha Patwa
Adrián Villalobos
Simon Weiler
Maxim Wintergoller
Nicolas Zdun
Anna Dudek
Heike Faust
Sabrina Heide
Ansgar Jahn
Linh Pham

Sachkova
Last Name: | Sachkova | Position: | MD-Student |
First Name: | Alexandra | Location: | Göttingen |
Academic Title: | Tel.: | ||
Tel.: | +49-(0)551/39-7995 |
Curriculum Vitae
Publications
2022
Repetitively burst-spiking neurons in reeler mice show conserved but also highly variable morphological features of layer Vb-fated “thick-tufted” pyramidal cells..
Jochen F. Staiger*, Alexandra Sachkova, Martin Möck, Julien Guy and Mirko Witte.
Front. Neuroanat. 16:1000107. doi: 10.3389/fnana.2022.1000107, 2022.
abstract link
Reelin is a large extracellular glycoprotein that is secreted by Cajal-Retziuscells during embryonic development to regulate neuronal migration andcell proliferation but it also seems to regulate ion channel distributionand synaptic vesicle release properties of excitatory neurons well intoadulthood. Mousemutants with a compromised reelin signaling cascade showa highly disorganized neocortex but the basic connectional features of thedisplaced excitatory principal cells seem to be relatively intact. Very little isknown, however, about the intrinsic electrophysiological and morphologicalproperties of individual cells in the reeler cortex. Repetitive burst-spiking (RB)is a unique property of large, thick-tufted pyramidal cells of wild-type layer Vbexclusively, which project to several subcortical targets. In addition, they areknown to possess sparse but far-reaching intracortical recurrent collaterals.Here, we compared the electrophysiological properties and morphologicalfeatures of neurons in the reeler primary somatosensory cortex with thoseof wild-type controls. Whereas in wild-type mice, RB pyramidal cells wereonly detected in layer Vb, and the vast majority of reeler RB pyramidal cellswere found in the superficial third of the cortical depth. There were noobvious dierences in the intrinsic electrophysiological properties and basicmorphological features (such as soma size or the number of dendrites) werealso well preserved. However, the spatial orientation of the entire dendritictree was highly variable in the reeler neocortex, whereas it was completelystereotyped in wild-typemice. It seems that basic quantitative features of layerVb-fated RB pyramidal cells are well conserved in the highly disorganizedmutant neocortex, whereas qualitative morphological features vary, possiblyto properly orient toward the appropriate input pathways, which are knownto show an atypical oblique path through the reeler cortex. The obliquedendritic orientation thus presumably reflects a re-orientation of dendriticinput domains toward spatially highly disorganized aerent projections.
2016
Intracortical Network Effects Preserve Thalamocortical Input Efficacy in a Cortex Without Layers.
Guy,J.; Sachkova,A.; Möck,M.; Witte,M.; Wagener,R.J.; Staiger,J.F..
Cerebral Cortex DOI 10.1093/cercor/bhw281, 2016.
abstract
Layer IV (LIV) of the rodent somatosensory cortex contains the somatotopic barrel field. Barrels receive much of the sensory input to the cortex through innervation by thalamocortical axons from the ventral posteromedial nucleus. In the reeler mouse, the absence of cortical layers results in the formation of mispositioned barrel-equivalent clusters of LIV fated neurons. Although functional imaging suggests that sensory input activates the cortex, little is known about the cellular and synaptic properties of identified excitatory neurons of the reeler cortex. We examined the properties of thalamic input to spiny stellate (SpS) neurons in the reeler cortex with in vitro electrophysiology, optogenetics, and subcellular channelrhodopsin-2-assisted circuit mapping (sCRACM). Our results indicate that reeler SpS neurons receive direct but weakened input from the thalamus, with a dispersed spatial distribution along the somatodendritic arbor. These results further document subtle alterations in functional connectivity concomitant of absent layering in the reeler mutant. We suggest that intracortical amplification mechanisms compensate for this weakening in order to allow reliable sensory transmission to the mutant neocortex
2012
Unique functional properties of somatostatin-expressing GABAergic neurons in mouse barrel cortex.
Gentet LJ, Kremer Y, Taniguchi H, Huang ZJ, Staiger J, Petersen CCH.
Nat Neurosci 15:607-612, 2012.
abstract link
Neocortical GABAergic neurons have diverse molecular, structural and electrophysiological features, but the functional correlates of this diversity are largely unknown. We found unique membrane potential dynamics of somatostatin-expressing (SOM) neurons in layer 2/3 of the primary somatosensory barrel cortex of awake behaving mice. SOM neurons were spontaneously active during periods of quiet wakefulness. However, SOM neurons hyperpolarized and reduced action potential firing in response to both passive and active whisker sensing, in contrast with all other recorded types of nearby neurons, which were excited by sensory input. Optogenetic inhibition of SOM neurons increased burst firing in nearby excitatory neurons. We hypothesize that the spontaneous activity of SOM neurons during quiet wakefulness provides a tonic inhibition to the distal dendrites of excitatory pyramidal neurons. Conversely, the inhibition of SOM cells during active cortical processing likely enhances distal dendritic excitability, which may be important for top-down computations and sensorimotor integration.