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Berriman-Rozen, Z. D.

Publications and source records attributed to Berriman-Rozen, Z. D..

2 recordsLinked to original sources

Amyloidosis and tauopathy progressively disrupt near-critical dynamics in selectively vulnerable circuits

Mechanistically distinct neurodegenerative diseases result in similar cognitive deficits, and pathology is often concentrated in a set of circuits known to be selectively vulnerable. Selective vulnerability is an intrinsic property of a circuit: in APP/PS1 mice, where plaques are global, functional disruptions are confined to circuits within the default mode network. What characterizes the dynamics of vulnerable circuits from those of spared circuits is unknown. We asked whether the distinguishing property is the proximity of population dynamics to criticality, a homeostatic set-point of network activity that determines computational capacity. We recorded single units simultaneously in three selectively vulnerable regions (retrosplenial cortex, anterior cingulate cortex, and CA1 hippocampus) and in primary visual cortex of freely behaving young and old APP/PS1 and wild-type mice. Firing rate and spike-time variability differed by genotype inconsistently across regions and ages. In contrast, three measures from criticality theory each revealed deficits that emerged only with age and only in the vulnerable regions. No measure detected a progressive change in V1. Avalanche scaling is not fixed in neural activity, but varies along a scaling line as the network state changes. As a result, the lines generated by each genotype revealed a constitutive effect of the transgene in young animals, which inverted with age in amyloid-bearing animals, but only in vulnerable circuits. If the destabilization of near-critical dynamics directly reflects a circuit's functional capacity, the same signature should identify a mechanistically distinct degenerative disease. In a model of tauopathy (P301S/E4), CA1 dynamics were displaced from the control scaling line with the same age-dependent reversal observed in APP/PS1. Our results suggest a network-level principle of neurodegenerative diseases: molecularly unrelated pathologies converge on the loss of near-critical dynamics in selectively vulnerable circuits.

neuroscience↗

A molecular integrator of sleep duration and interruption

Sleep is regulated across multiple timescales. Transitions between sleep and wake happen within seconds1,2; individual sleep bouts last minutes to hours3; and homeostatic sleep need has classically been tracked across multiple bouts4. Rapid sleep-to-wake transitions are driven by identified neurons, circuits, and neuromodulators1, while slow wave activity correlates with sleep need across hours5,6. However, no signal has been shown to encode sleep history within individual sleep bouts, the timescale at which the brain must continuously monitor how much sleep has occurred and how likely waking is at any given moment. Biochemical signals downstream of sleep/wake-associated neuromodulators display slower dynamics than the neuromodulators themselves7,8, making them candidate encoders of within-bout sleep history. Here, by measuring protein kinase A substrate phosphorylation (PKA-SP) in real time in freely behaving mice7-9, we show that membrane PKA-SP decreases exponentially within each sleep bout with consistent kinetics across bouts, integrates sleep duration and sleep interruption, and continuously forecasts moment-to-moment waking probability. Following sleep deprivation, PKA-SP reaches lower levels at the end of sleep bouts, correlating with increased sleep need dissipation. These findings identify a molecular signal encoding within-bout sleep history, revealing how biochemical dynamics bridge fast arousal circuits and the slow timescale of classical sleep homeostasis.

neuroscience↗