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Lau, C. G.

Publications and source records attributed to Lau, C. G..

3 recordsLinked to original sources

Automated behavior classification of julius seizure mutants in Drosophila reveals stereotyped seizure stages with genotype specificity

Bang-sensitive (BS) Drosophila mutants exhibit a stereotyped pattern of seizure behavior after mechanical disturbances. We previously identified mutations in the julius seizure (jus) gene, formerly CG14509, can induce BS seizures. However, the behavioral manifestations of the seizure phenotype of the various jus mutants have not been fully characterized. Here, we developed a machine learning pipeline featuring LASC (Long short-term memory and Attention mechanism for Sequence Classification) for automatic phenotyping of jus mutant videos. LASC achieves 90% classification accuracy in distinguishing five phases: paralysis (P), tonic seizure (T), spasm (S), clonic seizure (C), and recovery (R). Applying the trained LASC model to multiple jus lines showed they use a common repertoire of seizure stages and followed the general P[->]T[->]S[->]C[->]R progression, but each genotype exhibited unique patterns of stage duration and transition probabilities. Remarkably, stage usage patterns are distinct among the mutant genotypes. These findings establish that while all jus mutants adhere to stereotyped behavioral rules, each allele generates a distinct signature in stage usage. This work demonstrates how advanced behavioral quantification can reveal previously hidden relationships between gene mutation and complex motor outputs. More broadly, the complete pipeline presented here can pave the way for high-throughput, automated drug screening for epilepsy.

neuroscience↗

Suppression of piriform cortex alters brain-wide dynamics and alleviates seizures in temporal lobe epilepsy

BackgroundTemporal lobe epilepsy (TLE) involves aberrant changes in the brain at molecular, cellular and circuitry levels, leading to recurrent seizures. Approximately one-third of patients develop drug resistance. Circuit-based interventions show promise for alleviating the drug-resistant seizures. This study explored the efficacy of chemogenetic stimulation on specific neuronal populations in piriform cortical microcircuits in a mouse TLE model. ObjectiveThe anterior piriform cortex (APC) is a limbic area closely associated with TLE but is understudied. Our previous study demonstrated that in the APC, parvalbumin-expressing (PV+) interneurons provide strong inhibition and help maintain excitation-inhibition balance. Here, we examined whether and how APCPV neurons can ameliorate seizure symptoms in TLE. MethodsWe used a chronic intrahippocampal kainic acid (IHKA) mouse model that develops hippocampal pathology and spontaneous recurrent seizures (SRSs). APCPV neurons were chemogenetically activated, and local field potentials were recorded longitudinally from multiple regions. Seizure metrics, spectral power and functional connectivity were compared between APCPV-activated and control samples. ResultsLoss of PV+ synapses emerged in the APC during epileptogenesis. Selective activation of APCPV neurons reduced the frequency and duration of hippocampal SRSs and modified long-range dynamics, with region- and frequency-specific changes in interictal band power and functional connectivity. ConclusionAPCPV chemogenetic activation exerts a robust anti-seizure effect and identifies the APC as a promising cortical node for seizure network control. The associated spectral and connectivity signatures suggest that targeted modulation of APC microcircuits can rebalance distributed seizure networks and lower seizure recurrence.

neuroscience↗

Distinct projection patterns of different classes of layer 2 principal neurons in the olfactorycortex

Processing of olfactory information in the anterior piriform cortex (APC) is widely thought to be non-topographic due to distributed projections from the olfactory bulb (OB). Layer 2 principal neurons in the APC can be divided into 2 subtypes: semilunar (SL) and superficial pyramidal (SP) cells. Although it is known that SL and SP cells receive differential inputs from the OB, little is known about their projection pattern to downstream structures, such as the posterior piriform cortex (PPC). Here we examined feedforward and feedback axonal projections of SL and SP cells using a combination of mouse genetics, and retrograde labeling. Retrograde tracing from the OB or PPC showed that the APC projects to these higher and lower brain regions mainly through layer 2b cells, while dual-labeling revealed a sizeable fraction of cells extending collaterals to both target regions. Furthermore, a transgenic mouse line specifically labeling SL cells showed that they send profuse axonal projections to olfactory cortical areas, but not to the OB. These findings support a model in which information flow from SL to SP cells and back to the OB forms a hierarchical feedback circuit whereas the two cell types process recurrent and feedforward information in a parallel manner.

neuroscience↗