Doerner Julia F, Delling Markus, Clapham David E
Department of Cardiology, Howard Hughes Medical Institute, Boston Children's Hospital, Boston, United States.
Department of Neurobiology, Harvard Medical School, Boston, United States.
Elife. 2015 Dec 9;4:e11066. doi: 10.7554/eLife.11066.
The beating of motile cilia generates fluid flow over epithelia in brain ventricles, airways, and Fallopian tubes. Here, we patch clamp single motile cilia of mammalian ependymal cells and examine their potential function as a calcium signaling compartment. Resting motile cilia calcium concentration ([Ca] 170 nM) is only slightly elevated over cytoplasmic [Ca] (100 nM) at steady state. Ca changes that arise in the cytoplasm rapidly equilibrate in motile cilia. We measured Ca1 voltage-gated calcium channels in ependymal cells, but these channels are not specifically enriched in motile cilia. Membrane depolarization increases ciliary [Ca], but only marginally alters cilia beating and cilia-driven fluid velocity within short (~1 min) time frames. We conclude that beating of ependymal motile cilia is not tightly regulated by voltage-gated calcium channels, unlike that of well-studied motile cilia and flagella in protists, such as and .
活动纤毛的摆动在脑室、气道和输卵管的上皮细胞上产生流体流动。在这里,我们用膜片钳技术研究了哺乳动物室管膜细胞单个活动纤毛的情况,并探讨了它们作为钙信号区室的潜在功能。静息状态下活动纤毛的钙浓度([Ca]约为170 nM)仅比稳态时细胞质中的[Ca](约100 nM)略有升高。细胞质中出现的钙变化在活动纤毛中迅速达到平衡。我们测量了室管膜细胞中的Ca1电压门控钙通道,但这些通道在活动纤毛中并没有特异性富集。膜去极化会增加纤毛中的[Ca],但在短时间(约1分钟)内仅略微改变纤毛摆动和纤毛驱动的流体速度。我们得出结论,与原生生物中如 和 等经过充分研究的活动纤毛和鞭毛不同,室管膜活动纤毛的摆动不受电压门控钙通道的严格调控。