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Imrie, G.

Publications and source records attributed to Imrie, G..

2 recordsLinked to original sources

Astrocyte Store-Released Calcium Modulates Visual Cortex Synapse Development and Circuit Function.

Astrocytes, a major class of glial cells, are critical regulators of synapse development during early postnatal life. While dysregulation of this process is implicated in numerous neurological disorders, the precise mechanisms by which astrocytes guide synapse formation and maturation remain poorly understood. A central signaling pathway for astrocytes is the dynamic fluctuation of intracellular calcium (Ca2+), which can arise from various sources and modulate a wide range of downstream effects. A key astrocytic mechanism for integrating neuronal signals is the release of Ca2+ from endoplasmic reticulum stores mediated by the IP3 Receptor Type 2 (IP3R2). Although defects in this signaling pathway have been mainly linked to adult brain dysfunction, its role in shaping synaptic development, a period when astrocyte-neuronal communication is established, is largely unknown. Here, we investigated the role of IP3R2-mediated Ca2+ signaling in astrocyte-dependent regulation of synapse development in the mouse visual cortex. Using a combination of histological, molecular, and circuit-level approaches, we found that loss of astrocytic IP3R2 leads to significant deficits in the maturation of glutamatergic but not GABAergic synapses. These synaptic disruptions were accompanied by attenuated visually evoked neuronal activation and impaired behavioral responses to visual threat stimuli. We further show that astrocytic morphological complexity is diminished in the absence of IP3R2, suggesting that store-released Ca2+ is required for both the structural and functional maturation of astrocyte-neuron interactions. Our findings establish a critical role for astrocytic IP3R2-mediated Ca2+ signaling in shaping excitatory circuit development and the emergence of visually driven behaviors.

neuroscience↗

Pleiotropic function of the oca2 gene underlies the evolution of sleep loss and albinism in cavefish

Adaptation to novel environments often involves the evolution of multiple morphological, physiological and behavioral traits. One striking example of multi-trait evolution is the suite of traits that has evolved repeatedly in cave animals, including regression of eyes, loss of pigmentation, and enhancement of non-visual sensory systems [1,3]. The Mexican tetra, Astyanax mexicanus, consists of fish that inhabit at least 30 caves in Northeast Mexico and ancestral-like surface fish which inhabit the rivers of Mexico and Southern Texas [6]. Cave A. mexicanus are interfertile with surface fish and have evolved a number of traits that are common to cave animals throughout the world, including albinism, eye loss, and alterations to behavior [8-10]. To define relationships between different cave-evolved traits, we phenotyped 208 surface-cave F2 hybrid fish for numerous morphological and behavioral traits. We found significant differences in sleep between pigmented and albino hybrid fish, raising the possibility that these traits share a genetic basis. In cavefish and many other species, mutations in oculocutaneous albinism 2 (oca2) cause albinism [11-15]. Surface fish with CRISPR-induced mutations in oca2 displayed both albinism and reduced sleep. Further, this mutation in oca2 fails to complement sleep loss when surface fish harboring this engineered mutation are crossed to different, independently evolved populations of albino cavefish with naturally occurring mutations in oca2, confirming that oca2 contributes to sleep loss. Finally, analysis of the oca2 locus in wild caught cave and surface fish suggests that oca2 is under positive selection in at least three cave populations. Taken together, these findings identify oca2 as a novel regulator of sleep and suggest that a pleiotropic function of oca2 underlies the adaptive evolution of both of albinism and sleep loss.

evolutionary biology↗