Selective saccular plasticity under microgravity links peripheral transcriptomic remodeling to postflight vestibular dysfunction

球囊 太空飞行 胞囊 前庭系统 转录组 生物 耳石 神经科学 失重 神经可塑性 感觉系统 细胞生物学 内耳 解剖 前庭电刺激 基诺西林 显微神经学 半规管 蛋白质组 外围设备 机械反应 前庭核 突触可塑性
作者
Chikara Abe,Shin-ichiro Fujita,Dai Shiba,Kunihiko Tanaka,Chisato Fujimoto,Shigeto Tokunaga,Shinichi Iwasaki,Satoru Takahashi,Masafumi Muratani,Hironobu Morita
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:123 (35): e2605593123-e2605593123
标识
DOI:10.1073/pnas.2605593123
摘要

Long-duration exposure to microgravity disrupts human balance and spatial orientation, yet the molecular mechanisms underlying vestibular adaptation to spaceflight remain poorly understood. Here, we tested the hypothesis that the saccule, the primary gravity-sensing otolith organ, undergoes selective remodeling during spaceflight and contributes to transient postflight postural instability. Using a cross-species approach, we combined transcriptomic analysis of mouse otolith organs with physiological assessments in astronauts. Laser microdissection–based RNA sequencing of mouse otolith sensory epithelia after a 35-d spaceflight revealed pronounced, organ-specific transcriptomic remodeling in the saccule, whereas the utricle remained stable. Principal component and clustering analyses demonstrated that the saccular transcriptome shifted toward an utricle-like profile under microgravity, accompanied by changes in genes related to synaptic and neuronal function. Promoter motif analysis identified NFAT-associated transcriptional networks, suggesting Ca 2+ -dependent regulation of synaptic plasticity as a potential molecular substrate of gravity-dependent adaptation. In parallel, vestibular testing in astronauts following long-duration missions (157 to 328 d) revealed selective attenuation of saccule-mediated cervical vestibular-evoked myogenic potentials and increased postural sway immediately after return to Earth, while utricle-mediated responses and semicircular canal function were preserved. Both saccular function and postural stability recovered within approximately 10 d. Notably, early postflight postural instability was partially mitigated by noisy galvanic vestibular stimulation, consistent with stochastic resonance–mediated sensory enhancement. Together, these findings identify the saccule as a plastic gravity sensor and establish a mechanistic link between peripheral molecular remodeling and functional balance deficits after spaceflight, providing a framework for developing countermeasures to facilitate vestibular readaptation during human space exploration.
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