期刊
FEBS JOURNAL
卷 -, 期 -, 页码 -出版社
WILEY
DOI: 10.1111/febs.17024
关键词
Aurora A; calcium; optogenetics; primary cilia; store-operated Ca2+ entry
This study investigates the regulation of cytosolic Ca2+ levels on ciliogenesis and finds that Ca2+ influx inhibits ciliogenesis while Ca2+ depletion promotes ciliogenesis. Additionally, store-operated Ca2+ entry and the endoplasmic reticulum Ca2+ sensor STIM1 negatively regulate ciliogenesis. The effects of different Ca2+ oscillation patterns on ciliogenesis are also explored using an optogenetic platform.
The primary cilium is an antenna-like organelle protruding from the cell surface that can detect physical and chemical stimuli in the extracellular space to activate specific signaling pathways and downstream gene expressions. Calcium ion (Ca2+) signaling regulates a wide spectrum of cellular processes, including fertilization, proliferation, differentiation, muscle contraction, migration, and death. This study investigated the effects of the regulation of cytosolic Ca2+ levels on ciliogenesis using chemical, genetic, and optogenetic approaches. We found that ionomycin-induced Ca2+ influx inhibited ciliogenesis and Ca2+ chelator BATPA-AM-induced Ca2+ depletion promoted ciliogenesis. In addition, store-operated Ca2+ entry and the endoplasmic reticulum Ca2+ sensor stromal interaction molecule 1 (STIM1) negatively regulated ciliogenesis. Moreover, an optogenetic platform was used to create different Ca2+ oscillation patterns by manipulating lighting parameters, including density, frequency, exposure time, and duration. Light-activated Ca2+-translocating channelrhodopsin (CatCh) is activated by 470-nm blue light to induce Ca2+ influx. Our results show that high-frequency Ca2+ oscillations decrease ciliogenesis. Furthermore, the inhibition of cilia formation induced by Ca2+ may occur via the activation of Aurora kinase A. Cilia not only induce Ca2+ signaling but also regulate cilia formation by Ca2+ signaling.
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