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Puskas, J.

Publications and source records attributed to Puskas, J..

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Functional characterization of the lateral septal calbindin neurons in maternal care

The ventral subdivision of the lateral septum (LSv) is a forebrain region linked to maternal care with a high density of calbindin-containing (Cb+) neurons whose properties, connections and functions remain unknown. In the present study, it was established that the majority of pup-activated neurons are inhibitory Cb+ in the LSv and the density of activated neurons in the LSv is close to that of the medial preoptic area (MPOA), a central brain area in maternal care regulation. Electrophysiological recordings of LSvCb+ and LSvCb- neurons revealed that LSvCb+ neurons exhibited higher membrane resistance, lower spike amplitude and rise slope compared to LSvCb- neurons. The chemogenetic inhibition of LSvCb+ neurons led to reduction in pup-licking behavior without affecting other maternal behavior or eliciting anxiety- or depression-like behavior. To regulate licking behavior, LSvCb+ neurons connect with other maternally involved brain areas. Anterograde and retrograde tract-tracing revealed that two-thirds of the MPOA-projecting LSv neurons are Cb+. A subset of neurons within the posterior intralaminar nucleus (PIL) in the lateral thalamus, a proposed relay nucleus of tactile and auditory information from the pups, express a maternally induced neuropeptide, the parathyroid hormone 2 (PTH2). Their fibers closely apposed Cb+ neurons in the LSv. Using double labeling, we also identified PTH2 receptors on LSvCb+ neurons, which are presumably activated by PTH2 released from nearby terminals. Using electron microscopy, we confirmed synaptic connection between PTH2+ fibers and inhibitory neurons in the LSv. The results provide evidence that Cb+ neurons of the LSv are components of the maternal circuitry. Significance StatementMaternal care depends on pup cues, but many responsible circuit elements remain uncharacterized. We identify inhibitory calbindin-expressing neurons in the ventral subdivision of the lateral septum (LSv) containing a major pup-activated neuronal population with distinctive electrical properties. Their selective inhibition reduced pup-licking without affecting other maternal, anxiety- or depression-like behaviors, suggesting a specific role in caregiving. Detailed circuit tracing data revealed that a significant proportion of LSv calbindin-positive neurons extend their projections to the medial preoptic area, a well-established core maternal regulatory region. We further demonstrate synaptic input from maternally relevant parathyroid hormone 2 (PTH2)-expressing thalamic afferents onto LSv inhibitory neurons, possibly conveying pup stimuli. The data suggest that LSv calbindin neurons are key nodes in maternal circuitry.

neuroscience↗

Evaluating the Radiation Sensitivity Index and 12-chemokine gene expression signature for clinical use in a CLIA laboratory

BackgroundThe radiation sensitivity index (RSI) and 12-chemokine gene expression signature (12CK GES) are two gene expression signatures (GES) that were previously developed to predict tumor radiation sensitivity or identify the presence of tertiary lymphoid structures in tumors, respectively. To advance the use of these GES into clinical trial evaluation, their assays must be assessed within the context of the Clinical Laboratory Improvement Amendments (CLIA) process. MethodsUsing HG-U133Plus 2.0 arrays, we first established CLIA laboratory proficiency. Then the accuracy (limit of detection and macrodissection impact), precision (variability by time and operator), sample type (surgery vs. biopsy), and concordance with reference laboratory were evaluated. ResultsRSI and 12CK GES were reproducible (RSI: 0.01 mean difference, 12CK GES 0.17 mean difference) and precise with respect to time and operator. Taken together, the reproducibility analysis of the scores indicated a median RSI difference of 0.06 (6.47% of range) across samples and a median 12CK GES difference of 0.92 (12.29% of range). Experiments indicated that the lower limit of input RNA is 5 ng. Reproducibility with a second CLIA laboratory demonstrated reliability with the median RSI score difference of 0.065 (6% of full range) and 12CK GES difference of 0.93 (12 % of observed range). ConclusionsOverall, under CLIA, RSI and 12CK GES were demonstrated by the Moffitt Cancer Center Advanced Diagnostic Laboratory to be reproducible GES for clinical usage.

genomics↗