Biology subjects

Kullander, K.

Publications and source records attributed to Kullander, K..

10 recordsLinked to original sources

bioRxiv2026

Functional specialization of OLMα2 interneurons emerges from differential longitudinal hippocampal-amygdala wiring

The ventral hippocampus (vHipp) is increasingly recognized for its role in processing probabilistic threats and emotional salience, yet the circuit mechanisms underlying these computations remain unclear. Here, we investigated how oriens-lacunosum moleculare interneurons expressing the 2 subunit of the nicotinic acetylcholine receptor (OLM2 cells) contribute to hippocampal function along the longitudinal axis. Combining cell-type specific optogenetics, behavioral assays, monosynaptic and transsynaptic viral tracing, we compared intermediate hippocampal (iHipp) and vHipp OLM2 populations. We show that OLM2 cells exert regionally distinct control over behavior. Manipulation of iHipp OLM2 cells selectively influenced object-directed exploration and novel object processing without affecting anxiety-like behavior, whereas vHipp OLM2 cells modulated arousal and emotionally driven avoidance without contributing to object memory. Circuit tracing revealed that this functional double dissociation is paralleled by distinct connectivity profiles: iHipp is preferentially embedded in sensory cortical networks, whereas vHipp is strongly connected to limbic structures, including the basolateral amygdala and nucleus accumbens. Notably, despite robust regional amygdala-hippocampal connectivity, OLM2 interneurons themselves received sparse direct amygdala input, indicating that emotional modulation is mediated indirectly via hippocampal pyramidal cell pathways. In contrast, stimulation of basolateral amygdala projections to vHipp promoted approach behavior without inducing generalized aversion, further supporting pathway- and cell-type specific encoding of valence and salience. Together, our findings demonstrate that OLM2 interneurons implement a longitudinally organized inhibitory framework in which conserved microcircuit motifs yield distinct behavioral outcomes, depending on their embedding within region specific input and output networks. This work identifies a mechanistic basis for functional specialization along the hippocampal axis and highlights interneuron positioning as a key determinant of hippocampal contributions to cognition and emotion.

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bioRxiv2026

Layer 5 Martinotti and pyramidal neurons encode spatial information in the primary motor cortex

Mammals rely on external sensory cues and internal bodily signals to create a precise spatial awareness. The motor cortex is essential for this process, integrating proprioceptive and spatial information. Here, we investigate how layer 5 martinotti (M2) interneurons and pyramidal cells contribute to spatial processing in primary motor cortex (M1). Using miniscopes in freely moving mice expressing CaMKIIa-GCaMP8f or DIO-GCaMP8f in Chrna2-Cre+ mice, we recorded activity from both cell types. We found that both M2 and pyramidal cells are tuned to place, head direction, and grid fields, with distinct characteristics. Notably, both cell types exhibit an overrepresentation of co-tuned place- and head-direction responses compared to chance. Moverover, pyramidal head direction-tuned cells show sharper tuning than M2 head direction-tuned cells. Further, place-tuned M2 cells are more active, whereas pyramidal place-tuned cells showed reduced activity compared to non-place-tuned ones. Additionally, both cell types exhibit lower activity in head-direction-tuned compared to non-head direction-tuned cells. These findings suggest that distinct neural coding strategies are employed by different cell types within the M1 for processing spatial information, highlighting the complex neural mechanisms underlying spatial cognition.

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bioRxiv2025

Y-maze and Vertical Pole Performance Correlate with Fine Motor Learning in Mice

The relationships between distinct abilities and their interdependencies during memory tasks and motor learning activities are not clear. An important question is whether being proficient in memory or motor learning tasks also translates into better performance in another, similar task - reflecting potential generalization of motor learning abilities. To investigate the correlation between memory performance and motor learning, we used a combination of behavioral tasks that assess general exploratory behavior, declarative memory, and fine motor learning in female mice. For the exploratory behavior, we used the open field task, and assessed declarative memory using the novel object recognition and Y-maze. Motor performance and learning was assessed through the vertical pole and pellet reaching task. We found a positive correlation between the Y-maze and the pellet reaching task performance, where a higher exploration rate indicated a higher success ratio in the pellet reaching task. Further, leave-one-out cross-validation prediction analysis show that Y-maze performance is a robust predictor of pellet reaching performance, showing that mice pellet reaching performance can reliably be predicted from Y-maze performance. These results can be used to conduct a pre-study for challenging motor tasks that include pre-behavioral procedures on mice. Our study shows that performance in the Y-maze predicts pellet reaching performance, indicating that these tasks can be used as pre-screening for motor learning performance and activity.

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bioRxiv2025

Auditory regulation of hippocampal locomotion circuits by a non-canonical reticular-limbic pathway

The ability to rapidly detect and respond to unexpected auditory stimuli is critical for adaptive behavior, especially during locomotion. Since movement suppresses auditory cortical activity, it remains unclear how salient auditory information influences locomotor circuits. In this work, using in vivo calcium imaging, electrophysiology, chemo- and optogenetics, we investigate the path that relays loud broadband sounds to the dorsal hippocampus (dHPC) and modulates theta oscillations. We demonstrate that noise accelerates theta frequency and decreases its power, effects mediated by entorhinal cortex (EC) and medial septum (MS) inputs while independent of the primary auditory cortex. Activation of dorsal cochlear nucleus (DCN) neurons projecting to the pontine reticular nucleus (PRN) mimics noise-driven hippocampal responses, supporting a brainstem-limbic auditory processing route. Furthermore, noise selectively modulates CA1 pyramidal neuron and interneuron activity, reflecting diverse circuit dynamics. Finally, loud broadband noise stimulus increased theta coherence between the dHPC and the medial prefrontal cortex (mPFC), enhancing interregional synchronization. These results highlight the mechanisms in which the DCN filters behaviorally relevant sounds promoting acoustic motor integration in the hippocampus during locomotion, without direct influence of the auditory cortex.

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bioRxiv2024

Layer 5 Martinotti cell activation reduces pyramidal cell population plasticity and improves fine motor function

During motor activity and motor learning, pyramidal cells in the motor cortex receive inputs from local interneurons as well as deeper structures. Layer 5 pyramidal cells in the primary motor cortex then feed commands to spinal circuits for motor execution. The genetic ablation of layer 5 Chrna2 Martinotti cells, which selectively target pyramidal tract pyramidal cells, resulted in disturbed fine motor functions. Using calcium imaging combined with chemogenetics, we show that activation of layer 5 Chrna2 Martinotti cells during training increases pyramidal cell tuning, changes responses temporal patterns and decreases assembly reconfiguration, while not affecting motor learning success rates. However, in mice that had already learned a reach-and-grasp (prehension) task, Chrna2 Martinotti cell activation resulted in improved prehension and increased power in low theta and high gamma bands of local field potentials in the motor cortex. This work indicates that activation of Chrna2 Martinotti cells reduces pyramidal cell assembly plasticity during learning, possibly facilitating already acquired motor skills.

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bioRxiv2023

Functional specialization of hippocampal somatostatin-expressing interneurons

Hippocampal somatostatin-expressing (Sst) GABAergic interneurons (INs) exhibit considerable anatomical and functional heterogeneity. Recent single cell transcriptome analyses have provided a comprehensive Sst-IN subtype census, a plausible molecular ground truth of neuronal identity whose links to specific functionality remain incomplete. Here, we designed an approach to identify and access subpopulations of Sst-INs based on transcriptomic features. Four mouse models based on single or combinatorial Cre- and Flp- expression differentiated functionally distinct subpopulations of CA1 hippocampal Sst-INs that largely tiled the morpho-functional parameter space of the Sst-INs superfamily. Notably, the Sst;;Tac1 intersection revealed a population of bistratified INs that preferentially synapsed onto fast-spiking interneurons (FS-INs) and were both necessary and sufficient to interrupt their firing. In contrast, the Ndnf;;Nkx2-1 intersection identified a population of oriens lacunosum-moleculare (OLM) INs that predominantly targeted CA1 pyramidal neurons, avoiding FS-INs. Overall, our results provide a framework to translate neuronal transcriptomic identity into discrete functional subtypes that capture the diverse specializations of hippocampal Sst-INs. Significance statementGABAergic interneurons are important regulators of neuronal activity. Recent transcriptome analyses have provided a comprehensive classification of interneuron subtypes, but the connections between molecular identities and specific functions are not yet fully understood. Here, we developed an approach to identify and access subpopulations of interneurons based on features predicted by transcriptomic analysis. Functional investigation in transgenic animals revealed that hippocampal somatostatin-expressing interneurons (Sst-INs) can be divided into at least four subfamilies, each with distinct functions. Most importantly, the Sst;;Tac1 intersection targeted a population of bistratified cells that overwhelmingly targeted fast-spiking interneurons. In contrast, the Ndnf;;Nkx2-1 intersection revealed a population of oriens lacunosum-moleculare interneurons that selectively targeted CA1 pyramidal cells. Overall, this study reveals that genetically distinct subfamilies of Sst-INs form specialized circuits in the hippocampus with differing functional impact.

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bioRxiv2023

Unraveling the role of Slc10a4 in auditory processing and sensory motor gating: implications for neuropsychiatric disorders?

BackgroundPsychiatric disorders, such as schizophrenia, are complex and challenging to study, partly due to the lack of suitable animal models. However, the absence of the Slc10a4 gene, which codes for a monoaminergic and cholinergic associated vesicular transporter protein, in knockout mice (Slc10a4 -/-), leads to the accumulation of extracellular dopamine. This makes them a potential animal model for schizophrenia, a disorder known to be associated with altered dopamine signaling in the brain. MethodsThe locomotion, auditory sensory filtering and prepulse inhibition (PPI) of Slc10a4 -/- mice were quantified and compared to wildtype (WT) littermates. Intrahippocampal electrodes were used to record auditory event-related potentials (aERPs) for quantifying sensory filtering in response to paired-clicks. The channel above aERPs phase reversal was chosen for reliably comparing results between animals, and aERPs amplitude and latency of click responses were quantified. WT and Slc10a4 -/- mice were also administered subanesthetic doses of ketamine to provoke psychomimetic behavior. ResultsBaseline locomotion during auditory stimulation was similar between Slc10a4 -/- mice and WT littermates. In WT animals, normal auditory gating was observed after i.p saline injections, and it was maintained under the influence of 5 mg/kg ketamine, but disrupted by 20 mg/kg ketamine. On the other hand, Slc10a4 -/- mice did not show significant differences between N40 S1 and S2 amplitude responses in saline or low dose ketamine treatment. Auditory gating was considered preserved since the second N40 peak was consistently suppressed, but with increased latency. The P80 component showed higher amplitude, with shorter S2 latency under saline and 5 mg/kg ketamine treatment in Slc10a4 -/- mice, which was not observed in WT littermates. Prepulse inhibition was also decreased in Slc10a4 -/- mice when the longer interstimulus interval of 100 ms was applied, compared to WT littermates. ConclusionThe Slc10a4 -/- mice responses indicate that cholinergic and monoaminergic systems participate in the PPI magnitude, in the temporal coding (response latency) of the auditory sensory gating component N40, and in the amplitude of aERPs P80 component. These results suggest that Slc10a4 -/- mice can be considered as potential models for neuropsychiatric conditions.

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bioRxiv2020

Using cortical neuron markers to target cells in the dorsal cochlear nucleus

The dorsal cochlear nucleus (DCN) is the first auditory region that integrates somatosensory and auditory inputs. The region is of particular interest for auditory research due to the large incidence of somatic tinnitus and increased aberrant activity in other forms of tinnitus. Yet, the lack of useful genetic markers for in vivo manipulations hinders the elucidation of the DCN contribution to tinnitus pathophysiology. In this work, we assessed whether adeno-associated viral vectors (AAV) containing the calcium/calmodulin-dependent protein kinase 2 alpha (CaMKII) promoter and our mouse line of nicotinic acetylcholine receptor alpha 2 subunit (Chrna2)-Cre can be used to target specific DCN populations. The CaMKII promoter is usually applied in studies of principal neurons of neo and paleocortex while Chrna2-cre mice express Cre recombinase in cortical dendrite inhibiting interneurons. We found that CaMKII cannot be used to specifically target excitatory fusiform DCN neurons. EYFP expression driven by the CaMKII promoter was stronger in the fusiform layer but labelled cells showed a diverse morphology indicating that they belong to different classes of DCN neurons. Light stimulation after driving Channelrhodopsin2 (ChR2) by the CaMKII promoter generated spikes in some units but firing rate decreased when light stimulation coincide with sound presentation. Expression and activation of eArch3.0 (CaMKII driven) in the DCN produced spike inhibition in some units but, most importantly, sound-driven spikes were delayed by concomitant light stimulation. We explored the existence of Cre+ cells in the DCN of Chrna2-Cre mice by hydrogel embedding technique (CLARITY). There were almost no Cre+ cell bodies in the DCN; however, we observed profuse projections arising from the ventral cochlear nucleus (VCN). Anterograde labeling Cre dependent AAV injected in the VCN revealed two main projections: one arising in the ipsilateral superior olive and the contralateral medial nucleus of the trapezoid body (bushy cells) and a second bundle terminating in the DCN, suggesting the latter to be excitatory Chrna2+ T-stellate cells). Stimulating ChR2 expressing terminals (light applied on the DCN) of VCN Chrna2+ cells increased firing of sound responding and nonresponding DCN units. This work shows that molecular tools intensively used in cortical studies may be useful for manipulating the DCN especially in tinnitus studies.

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bioRxiv2020

A point mutation in Ttc26 causes lumbar spinal cord fusion and synchronous hind-limb locomotion in hop mice

Identifying the spinal circuits controlling locomotion is critical for unravelling the mechanisms controlling the production of gaits. Development of the circuits governing left-right coordination relies on axon guidance molecules such as ephrins and netrins. To date, no other class of proteins have been shown to play a role during this process. Here we have analyzed hop mice, which walk with a characteristic hopping gait using their hind legs in synchrony. Fictive locomotion experiments suggest that a local defect in the ventral spinal cord contributes to the aberrant locomotor phenotype. Hop mutant spinal cords had severe morphological defects, including the absence of the ventral midline and a poorly defined border between white and grey matter. The hop mice represent the first model where the left and right central pattern generators (CPGs) are fused to form one central CPG, with a synchronous gait as a functional consequence. These defects were exclusively found in the lumbar domain and were associated with abnormal developmental processes, including a misplaced notochord and reduced induction of ventral progenitor domains. While the underlying mutation in hop mice has been suggested to lie within Ttc26, other genes in close vicinity have been associated with gait defects. By replicating the point mutation within Ttc26, employing CRISPR technology, we observed mice with an identical phenotype, thereby verifying the hop mutation. Thus, we show that the assembly of the lumbar CPG network is dependent on a fully functional TTC26 protein.

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bioRxiv2017

Loss of Wt1 in the murine spinal cord alters interneuron composition and locomotion

Rhythmic and patterned locomotion is driven by spinal cord neurons that form neuronal circuits, referred to as central pattern generators (CPGs). Recently, dI6 neurons were suggested to participate in the control of locomotion. The dI6 neurons can be subdivided into three populations, one of which expresses the Wilms tumor suppressor gene Wt1. However, the role that Wt1 exerts on these cells is not understood. Here, we aimed to identify behavioral changes and cellular alterations in the spinal cord associated with Wt1 deletion. Locomotion analyses of mice with neuron-specific Wt1 deletion revealed that these mice ran slower than controls with a decreased stride frequency and an increased stride length. These mice showed changes in their fore-hindlimb coordination, which were accompanied by a loss of contralateral projections in the spinal cord. Neonates with Wt1 deletion displayed an increase in uncoordinated hindlimb movements and their motor neuron output was arrhythmic with a decreased frequency. The population size of dI6, V0 and V2a neurons in the developing spinal cord of conditional Wt1 mutants was significantly altered. These results show that the development of particular dI6 neurons depends on Wt1 expression and loss of Wt1 is associated with alterations in locomotion.

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