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Krohn, K.

Publications and source records attributed to Krohn, K..

3 recordsLinked to original sources

An inhibitory feedback circuit mediating sleep need and sensory gating in Drosophila

Many animals integrate sensory information during the day and sleep at night. How sensory processing during wakefulness contributes to making an organism tired at night, however, remains elusive. Here, we investigate the role of excitatory helicon cells in Drosophila (ExR1), a distinct neural population dedicated to processing sensory information. Using combined optogenetics and voltage imaging, we show that helicon cells excite sleep-promoting R3m ring neurons and trigger a subsequent autoinhibition of R3m via voltage- and Ca2+-gated K+ channels such as Slowpoke. Investigating the flies sleep patterns, we found that blocking synaptic output from helicon as well as RNAi-mediated knockdown of Slowpoke in R3m reduces sleep quality and leads to loss of nocturnal sleep, indicating that sleep need is generated via this route. Further, we show that excitation of R3m induces feedback inhibition of helicon cells via ionotropic GABA receptors. Knockdown of the ionotropic GABA receptor subunit Rdl in helicon cells increases sleep latency and causes sleep loss at the beginning of the night. We show that inhibition via Rdl facilitates nocturnal slow-wave activity which forms a sensory filter and prevents sleep disruption through auditory stimuli. We therefore uncover an inhibitory feedback circuit, in which neurons processing sensory information directly activate sleep promoting neurons to generate sleep need. At night, this sleep need is then converted into actual sleep, facilitated by the formation of a neural filter that stabilizes sleep/wake transition.

neuroscience↗

A Germinal Center Checkpoint of AIRE in B Cells LimitsAntibody Diversification

In response to antigens, B cells undergo antibody diversification, including affinity maturation and class switching, mediated by activation-induced cytidine deaminase (AID) in secondary lymphoid organs, but uncontrolled AID activity can precipitate autoimmunity and cancer. The regulation of antibody diversification is of fundamental importance, though the mechanisms underlying these pathways are not well understood. We found that autoimmune regulator (AIRE), the molecule essential for T cell tolerance, is expressed in germinal center (GC) B cells in a CD40-dependent manner, interacts with AID and negatively regulates antibody affinity maturation and class switching by inhibiting AID function. AIRE deficiency in B cells caused altered antibody repertoire, increased somatic hypermutations, elevated autoantibodies to T helper 17 effector cytokines and defective control of skin Candida albicans. These results define a GC B cell checkpoint of humoral immunity and illuminate new approaches of generating high-affinity neutralizing antibodies for immunotherapy.

immunology↗

Drosophila Bchs overexpression recapitulates human WDFY3 neurodevelopmental phenotypes with implications for glial cell involvement in altered head circumference

The autophagy adaptor WDFY3 is linked to neurodevelopmental delay and altered brain size. Loss-of-function variants are associated with an increased brain size in both humans and mice. We thus, hypothesized that the microcephaly observed in some of the patients may be related to a gain-of-function of the WDFY3 gene product. While the role of WDFY3 loss-of-function has been studied extensively in neurons, little is known about the effects of WDFY3 overexpression in different neural cell types. We utilized a Drosophila melanogaster overexpression model to investigate the effect of the WDFY3 ortholog Bchs (blue cheese) on development, CNS size, and gene expression profiles. Glial and neuronal overexpression of Bchs impaired CNS development, locomotion and autophagy. Glial overexpression of Bchs also altered CNS size significantly. We identified 79 genes that were differentially expressed and overlapped in flies that overexpress Bchs in glial and neuronal cells, respectively. Additionally, upon neuronal Bchs overexpression differentially expressed genes clustered in gene ontology categories associated with autophagy and mitochondria. Our data indicate that WDFY3/Bchs overexpression in both neurons and glial cells results in impaired neural development, which corresponds to symptoms observed in WDFY3-related neurodevelopmental delay.

neuroscience↗