Dual-color live imaging unveils stepwise organization of multiple basal body arrays by cytoskeletons.
Gen ShiratsuchiSatoshi KonishiTomoki YanoYuichi YanagihashiShogo NakayamaTatsuya KatsunoHiroka KashiharaHiroo TanakaKazuto TsukitaKoya SuzukiElisa HerawatiHitomi WatanabeToyohiro HiraiTakeshi YagiGen KondohShimpei GotohAtsushi TamuraSachiko TsukitaPublished in: EMBO reports (2024)
For mucociliary clearance of pathogens, tracheal multiciliated epithelial cells (MCCs) organize coordinated beating of cilia, which originate from basal bodies (BBs) with basal feet (BFs) on one side. To clarify the self-organizing mechanism of coordinated intracellular BB-arrays composed of a well-ordered BB-alignment and unidirectional BB-orientation, determined by the direction of BB to BF, we generated double transgenic mice with GFP-centrin2-labeled BBs and mRuby3-Cep128-labeled BFs for long-term, high-resolution, dual-color live-cell imaging in primary-cultured tracheal MCCs. At early timepoints of MCC differentiation, BB-orientation and BB-local alignment antecedently coordinated in an apical microtubule-dependent manner. Later during MCC differentiation, fluctuations in BB-orientation were restricted, and locally aligned BB-arrays were further coordinated to align across the entire cell (BB-global alignment), mainly in an apical intermediate-sized filament-lattice-dependent manner. Thus, the high coordination of the BB-array was established for efficient mucociliary clearance as the primary defense against pathogen infection, identifying apical cytoskeletons as potential therapeutic targets.