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Rogers, F. D.

Publications and source records attributed to Rogers, F. D..

4 recordsLinked to original sources

Estrogen remodels large-scale cortical dynamics to promote behavioral persistence

Sex-steroid hormones remodel the brain on slow timescales of hours to days to coordinate adaptive behaviors with changing bodily physiology. Yet how this slow remodeling reorganizes and constrains neural computations that govern behavior on a moment-to-moment timescale remains poorly understood, particularly in cortical regions that support flexible social decision-making. Here we combined longitudinal high-density neural recordings, quantitative behavioral phenotyping and estrogen-receptor manipulation in female mice across low and high estrogen states. Tracking behavior and neural dynamics using this dense sampling approach revealed that high estrogen increased signatures of behavioral and neural persistence. High estrogen reversibly increased male-directed social preference and behavioral persistence, effects that were abolished by estrogen receptor alpha knockdown in the medial prefrontal cortex. In the mPFC high estrogen produced more persistent neural states that were more closely aligned with ongoing behavior, increased state discriminability, and compressed within-state dimensionality. At the single-neuron level, estrogen increased tuning selectivity, lengthened intrinsic timescales, and stabilized social representations across days, even within the same neurons tracked longitudinally. High estrogen also strengthened recurrent connectivity during the resting state, exhibiting preferential connectivity between similarly tuned ensembles. Finally, incorporating these connectivity changes into a mean-field dynamical-systems model was sufficient to reproduce increased behavioral and neural-state persistence. Together, these findings show that estrogen oscillates cortical computations across multi-day timescales, flipping the prefrontal cortex from flexible to persistent regimes that play a role in sustaining potentially costly social behaviors.

neuroscience↗

Agouti integrates environmental information to regulate natural variation in paternal behavior

Male investment in offspring rearing through paternal care is rare among mammals and the neural mechanisms governing its emergence are poorly understood. We leveraged the natural paternal behavior of African striped mice (Rhabdomys pumilio) in combination with brain-wide cFos quantification, single-nucleus RNA-sequencing, viral-mediated gene manipulation, and environmental manipulation to dissect the neural basis of natural variation in male parenting. We find that socio-environmental conditions drive individual variation in male alloparenting such that post-weaning social isolation increases paternal care while social living in higher density groups increases infanticide. This natural variation in care corresponds to neural activity in the medial preoptic area and changes in correlated activity across brain regions. Within the medial preoptic area, expression of agouti signaling protein (Agouti) in neurons is increased by group housing and is negatively associated with care, and overexpression of Agouti reduces care and enhances infanticide in previously tolerant animals. Naturalistic manipulations further reveal that Agouti integrates long-term housing conditions rather than food availability/hunger. Together, our results demonstrate that Agouti acts as a molecular integrator of socio-environmental information to drive variation in paternal care.

neuroscience↗

Thyroid hormones mediate the impact of early-life stress on ventral tegmental area gene expression and behavior

Proper thyroid function is essential to the developing brain, including dopamine neuron differentiation, growth, and maintenance. Stress across the lifespan impacts thyroid hormone signaling and anxiety disorders and depression have been associated with thyroid dysfunction (both hypo- and hyper-active). However, less is known about how stress during postnatal development impacts thyroid function and related brain development. Our previous work in mice demonstrated that early-life stress (ELS) transiently impinged on expression of a transcription factor in dopamine neurons shown to be regulated by thyroid hormones. We hypothesized that thyroid hormone signaling may link experience of ELS with transcriptional dysregulation within the dopaminergic midbrain, and ultimately behavior. Here, we find that ELS transiently increases thyroid-stimulating hormone levels (inversely related to thyroid signaling) in both male and female mice at P21, an effect which recovers by adolescence. We next tested whether transient treatment of ELS mice with synthetic thyroid hormone (levothyroxine, LT4) could ameliorate the impact of ELS on sensitivity to future stress, and on expression of genes related to dopamine neuron development and maintenance, thyroid signaling, and plasticity within the ventral tegmental area. Among male mice, but not females, juvenile LT4 treatment prevented hypersensitivity to adult stress. We also found that rescuing developmental deficits in thyroid hormone signaling after ELS restored levels of some genes altered directly by ELS, and prevented alterations in expression of other genes sensitive to the second hit of adult stress. These findings suggest that thyroid signaling mediates the deleterious impact of ELS on VTA development, and that temporary treatment of hypothyroidism after ELS may be sufficient to prevent future stress hypersensitivity.

neuroscience↗

Oxytocin receptor is not required for social attachment in prairie voles

Prairie voles are among a small group of mammals that display long-term social attachment between mating partners. Many pharmacological studies show that signaling via the oxytocin receptor (OxtR) is critical for the display of social monogamy in these animals. We used CRISPR-mutagenesis to independently generate three different OxtR null mutant prairie vole lines. OxtR mutants displayed social attachment such that males and females showed a behavioral preference for their mating partners over a stranger of the opposite sex when assayed using different paradigms. Mothers lacking OxtR delivered viable pups, and parents displayed care of their young and raised them to the weanling stage. Together, our studies unexpectedly reveal that OxtR-mediated signaling is genetically dispensable for social attachment, parturition, and parental behavior.

animal behavior and cognition↗