Biology subjects

Froemke, R.

Publications and source records attributed to Froemke, R..

9 recordsLinked to original sources

bioRxiv2026

A collicular-hypothalamic pathway for social visual awareness

Awareness of other individuals is a foundational element of social behavior. Here we examined how specific neural systems detect and signal the visual presence of conspecifics related to social arousal and motivation. We found that visual exposure to videos of other mice can activate hypothalamic oxytocin neurons and promote onset of pup retrieval behavior in naive virgin female mice. A range of social videos depicting conspecifics in diverse contexts, including but not limited to parental behavior, could accelerate onset of pup retrieval compared to non-social controls. Animals would elect to watch social videos over non-social videos. We made photo-tagged recordings from oxytocin neurons of the paraventricular nucleus (PVN), which were preferentially activated during social video viewing. Optogenetic silencing of PVN oxytocin neurons during exposure prevented this behavioral enhancement of pup retrieval onset. We also made photo-tagged recordings from a population of PVN-projecting neurons of the superficial superior colliculus (sSC[->]PVN units). Compared to other sSC neurons, the sSC[->]PVN neurons had specialized horizontal direction tuning with robust and sustained responses to social videos. sSC[->]PVN neurons differentiated visual scenes based on social content, responding most strongly to pup retrieval and less to scenes with increasing numbers of animals. Our results identify a subcortical visual pathway that signals the presence and salience of conspecifics to the oxytocin system, providing a circuit mechanism by which social visual awareness drives neuroendocrine arousal and the acquisition of parental behavior.

neuroscience↗

bioRxiv2024

Integrin-deficient T cell leukemia accumulates in the central nervous system

T-cell acute lymphoblastic leukemia (T-ALL) spreads aggressively to the central nervous system (CNS), particularly the leptomeninges. Children with T-ALL are treated with high-dose, CNS-directed chemotherapy, which can cause lasting neurotoxicity and is not always effective. Little is known about how T-ALL enters and persists within the CNS. However, normal T cell migration into the CNS has been extensively studied. Two integrins--VLA-4 and LFA-1--mediate normal T cell entry to the CNS, and VLA-4 blockade effectively treats multiple sclerosis by excluding T cells from the brain. We hypothesized that these integrins would likewise be required for T-ALL CNS entry. Unexpectedly, not only were VLA-4 and LFA-1 dispensable for T-ALL to reach the CNS, integrin-deficient T-ALL accumulated in the CNS compared to control. Mechanistically, integrin loss accelerated T-ALL proliferation in the CNS, suggesting that integrin-mediated interactions may promote quiescence in this space. Integrin blockade synergized with chemotherapy targeting proliferating cells, raising the possibility that combination therapy might be a powerful strategy.

immunology↗

bioRxiv2023

Auditory corticofugal circuits drive vocalization-guided maternal behavior

New parents become highly responsive to infant cries in parallel with auditory cortical plasticity enhancing representations of these calls. To promote caretaking behavior while controlling overall excitability, increased neural activity must be appropriately routed to downstream areas in combination with suppression of circuits that could promote aberrant behavioral responses. We investigated responses to multi-syllable mouse pup calls in cortical output neurons projecting to either the auditory striatum or auditory midbrain (inferior colliculus) using longitudinal 2-photon imaging and in vivo optically-tagged whole-cell recordings. Corticocollicular but not corticostriatal projections responded to pup calls over extended durations and were required for pup retrieval behavior, suggesting that these output units integrated multiple call syllables. The two populations diverged with parental experience, enhancing sustained responses in corticocollicular projections and reduced responses in corticostriatal projections. We performed simultaneous Neuropixels recordings from auditory cortex, thalamus, and midbrain to examine the temporal structure of call responses across areas and to dissect the influences of feedforward and feedback processing. Facilitation of later syllables increased in midbrain of maternally-experienced animals, together with reduced firing rates in a subset of units that were weakly coupled to cortical and midbrain activity. Overall, maternal experience leads to broad suppression of subcortical excitation in response to pup calls while selectively unmasking a subset of midbrain neurons that integrate over multiple syllables.

neuroscience↗

bioRxiv2022

Optopharmacological tools for precise spatiotemporal control of oxytocin signaling in the central nervous system and periphery

Oxytocin is a neuropeptide critical for maternal physiology and social behavior, and is thought to be dysregulated in several neuropsychiatric disorders. Despite the biological and neurocognitive importance of oxytocin signaling, methods are lacking to activate oxytocin receptors with high spatiotemporal precision in the brain and peripheral mammalian tissues. Here we developed and validated caged analogs of oxytocin which are functionally inert until cage release is triggered by ultraviolet light. We examined how focal versus global oxytocin application affected oxytocin-driven Ca2+ wave propagation in mouse mammary tissue. We also validated the application of caged oxytocin in the hippocampus and auditory cortex with electrophysiological recordings in vitro, and demonstrated that oxytocin uncaging can accelerate the onset of mouse maternal behavior in vivo. Together, these results demonstrate that optopharmacological control of caged peptides is a robust tool with spatiotemporal precision for modulating neuropeptide signaling throughout the brain and body.

neuroscience↗

bioRxiv2022

Input-Specific Inhibitory Plasticity Improves Decision Accuracy Under Noise

Inhibitory interneurons regulate excitability, information flow, and plasticity in neural circuits. Inhibitory synapses are also plastic and can be modified by changes in experience or activity, often together with changes to excitatory synapses. However, given the diversity of inhibitory cell types within the cerebral cortex, it is unclear if plasticity is similar for various inhibitory inputs or what the functional significance of inhibitory plasticity might be. Here we examined spike-timing-dependent plasticity of inhibitory synapses from four major subtypes of GABAergic cells onto layer 2/3 pyramidal cells in mouse auditory cortex. The likelihood of inhibitory potentiation varied across cell types, with somatostatin-positive (SST+) interneuron inputs exhibiting the most potentiation on average. A network simulation of perceptual decision-making revealed that plasticity of SST+-like inputs provided robustness from higher input noise levels to maintain decision accuracy. Differential plasticity at specific inhibitory inputs therefore may be important for network function and sensory perception.

neuroscience↗

bioRxiv2022

Oxytocin attenuates microglial activation and restores social and non-social memory in the APP/PS1 mouse model of Alzheimer's disease

Alzheimers disease (AD) is the main cause of dementia in the elderly and is characterized by memory loss, social withdrawal and neurodegeneration, eventually leading to death. Brain inflammation has emerged as a key pathogenic mechanism in AD. We hypothesized that oxytocin, a pro-social hypothalamic neuropeptide with anti-inflammatory properties, could have therapeutic actions in AD. We investigated oxytocin production in mouse models of AD, and evaluated the therapeutic potential of intranasal oxytocin. We observed lower levels of hypothalamic oxytocin in wild-type mice following brain infusion of amyloid-{beta} oligomers (A{beta}Os), as well as in APP/PS1 AD model mice. Treatment of APP/PS1 mice with intranasal oxytocin reduced microglial activation and favored deposition of A{beta} in dense core plaques, a potentially neuroprotective mechanism. Oxytocin further alleviated social and non-social memory impairments in APP/PS1 mice. Our findings point to oxytocin as a potential therapeutic target to reduce brain inflammation and correct memory deficits in AD.

neuroscience↗

bioRxiv2020

Innate sensitivity and plastic mechanisms in auditory cortex for reliable maternal behavior

Infant cries evoke powerful responses in parents1-4. To what extent are parental animals innately sensitive to neonatal vocalizations, or might instead learn about key vocal cues for appropriate parenting responses? In mice, naive virgins do not recognize the meaning of pup distress calls, but begin to retrieve pups to the nest following cohousing with a mother and litter5-8. These isolation calls can be variable, requiring co-caring virgins to generalize across features for reliable retrieval9, 10. Here, using behavioral studies combined with two-photon imaging and whole-cell recordings, we show that the onset of maternal behavior in mice results from the interaction between innate sensitivities and experience-dependent processes. We found that pup calls with inter-syllable intervals (ISIs) ranging from 75 to 375 ms elicited pup retrieval, and experienced auditory cortex generalized across these ISIs. In contrast, naive cortex was narrowly tuned to the most common or prototypical ISIs due to enhanced short-term depression of inhibitory inputs. Behavioral testing revealed that naive virgins were also more sensitive to prototypical calls than calls at other rates. Inhibitory and excitatory spiking and synaptic responses were initially mismatched in naive cortex, with untuned inhibition and overly-narrow excitation. Monitoring neuronal populations over cohousing revealed that excitatory neuronal responses broadened to represent a wide range of ISIs, while inhibitory neurons sharpened to form a perceptual boundary. Finally, we presented synthetic calls during cohousing and observed that neural and behavioral responses adjusted to match these statistics. Using inhibitory optogenetics, we found that auditory cortical activity was required to learn about specific features, whereas the oxytocinergic system was generally recruited for retrieval learning and plasticity in temporal tuning. Neuroplastic mechanisms therefore build on an innate sensitivity in the auditory cortex, enabling rapid plasticity for reliable parenting behavior.

neuroscience↗

bioRxiv2019

Oxytocin Neurons Enable Social Transmission of Maternal Behavior

Maternal care is profoundly important for mammalian survival, and non-biological parents can express it after experience with infants. One critical molecular signal for maternal behavior is oxytocin, a hormone centrally released by hypothalamic paraventricular nucleus (PVN). Oxytocin enables plasticity within the auditory cortex, a necessary step for responding to infant vocalizations. To determine how this change occurs during natural experience, we continuously monitored homecage behavior of female virgin mice co-housed for days with an experienced mother and litter, synchronized with recordings from virgin PVN cells, including from oxytocin neurons. Mothers engaged virgins in maternal care by ensuring their nest presence, and demonstrated maternal behavior in self-generated pup retrieval episodes. These social interactions activated virgin PVN and gated behaviorally-relevant cortical plasticity for pup vocalizations. Thus rodents can acquire maternal behavior by social transmission, and our results describe a mechanism for adapting brains of adult caregivers to infant needs via endogenous oxytocin. One Sentence SummaryMother mice help co-housed virgins become maternal by enacting specific behaviors that activate virgin oxytocin neurons.

neuroscience↗

bioRxiv2018

Heterosynaptic Plasticity Normalizes Cortical Excitatory-Inhibitory Balance

Excitation in neural circuits must be carefully controlled by inhibition to regulate information processing and network excitability. During development, cortical inhibitory and excitatory inputs are initially mismatched but become co-tuned or balanced with experience. However, little is known about how excitatory-inhibitory balance is defined at most synapses, or the mechanisms for establishing or maintaining this balance at specific set-points. Here we show how coordinated long-term plasticity calibrates populations of excitatory/inhibitory inputs onto mouse auditory cortical pyramidal neurons. Pairing pre- and postsynaptic activity induced plasticity at paired inputs and different forms of heterosynaptic plasticity at the strongest unpaired synapses, which required minutes of activity and dendritic Ca2+ signaling to be computed. Theoretical analyses demonstrated how the relative rate of heterosynaptic plasticity could normalize and stabilize synaptic strengths to achieve any possible excitatory-inhibitory correlation. Thus excitatory-inhibitory balance is dynamic and cell-specific, determined by distinct plasticity rules across multiple excitatory and inhibitory synapses.

neuroscience↗