023 Sleep in a Brainless Animal - The Relationship Between Centralization and Sleep in the Upside-down Jellyfish. (3rd May 2021)

• Record Type: Journal Article
• Authors: Abrams, Michael
• Is Part Of: Sleep. Volume 44(2021)Supplement 2
• Page Start: A11
• Page End: A11
• Publication Date: 2021-05-03
• Subjects: Sleep -- Physiological aspects -- Periodicals; Sleep disorders -- Periodicals; Sommeil -- Aspect physiologique -- Périodiques; Sommeil, Troubles du -- Périodiques; Sleep disorders; Sleep -- Physiological aspects; Sleep -- physiological aspects; Sleep Wake Disorders; Psychophysiology; Electronic journals; Periodicals; 616.8498
• DOI: 10.1093/sleep/zsab072.022
• Languages: English
• ISSNs: 0161-8105

Abstract

Abstract: Introduction: Though sleep is pervasive in animals, its fundamental roles, and the processes involved in generating the behavior, remain poorly understood. A key outstanding question in sleep regulation is whether sleep is controlled strictly by a top-down mechanism via activity of specific central nervous system (CNS) neurons or is controlled partially by bottom-up signals from neural and non-neural tissue. Recently, we showed that the upside-down jellyfish Cassiopea sleeps, providing an opportunity to study sleep control, regulation, and function in an animal without a CNS. Methods: Cassiopea have a decentralized nervous system (DNS) of radially spaced interconnected ganglia called rhopalia along their bell margin that control muscle contractions. The signal to contract is sent to muscle fibers local to the initiating ganglion, and the contraction propagates outwards as a point source wave. We have developed computer programs to detect the controlling ganglion, which allows us to non-invasively determine ganglia activity, and to understand how a simple network of ganglia controls behavior. We are also using immunofluorescence, in situ hybridization, qPCR, and RNAseq to characterize the effect of sleep deprivation (SD) on the jellyfish nervous system. Results: We have discovered a temporally centralized form of behavioral control that changes between day and night, and during SD. A subset of ganglia share behavioral control—while some almost never initiate contractions, others are active both day and night, or are mostly day-active or night-active, and SD drastically changes ganglia usage. Regions that increase activity at night are less active the following day, perhaps evidence of homeostatic regulation. Using RNAseq we found that during SD, one nAChRα subunit increases expression ~3.8-fold and we are studying its role in arousal and sleep. Conclusion: We are investigating a different kind of nervous system, one that is morphologically decentralized (a network of discrete ganglia), and yet temporally centralized (a subset of ganglia dominate activity control). Wake, sleep, and SD involve different ganglia activity patterns, different levels of centralization, and different gene expression. Thus, temporal centralization could provide a mechanism to explain how local sleep, via a bottom-up mechanism, can result in organismal sleep behavior. Support (if any): UC Berkeley Miller Postdoctoral Fellowship