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Ciliates utilise motile cilia, which are highly dynamic organelles protruding from the cell surface, to swim helically in a three-dimensional (3D) space. The 3D nature of its swimming behaviour and rapid ciliary beatings make its quantitative analysis difficult. Here, we quantified the 3D motion of a microbead bound to a ciliary tip in the live, immobilised Tetrahymena thermophila cell using 3D tracking optical microscopy. We found that the tip of individual ciliate cilia, consisting of the 9+2 structure of the axoneme, shows semicircular counterclockwise rotation in a single plane when looking down on the cilium. The rotational trajectories of the tip consist of fast and slow strokes, with the tip path during the fast and slow strokes being an arc and a linear, respectively. The direction of the fast stroke of the ciliary tip, with respect to the cell body, was from the right-anterior to the left-posterior region, which is consistent with the direction that could induce right-handed helical swimming of the Tetrahymena.
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http://dx.doi.org/10.1242/jcs.264027 | DOI Listing |
J Cell Sci
August 2025
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, 3-8- 1 Komaba, Meguro-ku, Tokyo 153-8902, Japan.
Ciliates utilise motile cilia, which are highly dynamic organelles protruding from the cell surface, to swim helically in a three-dimensional (3D) space. The 3D nature of its swimming behaviour and rapid ciliary beatings make its quantitative analysis difficult. Here, we quantified the 3D motion of a microbead bound to a ciliary tip in the live, immobilised Tetrahymena thermophila cell using 3D tracking optical microscopy.
View Article and Find Full Text PDFPLoS Biol
July 2025
Department of Molecular Biology and Genetics, Koç University, Istanbul, Turkey.
The primary cilium is a conserved, microtubule-based organelle that transduces signaling pathways essential for development and homeostasis. It dynamically assembles and disassembles in response to intrinsic and extrinsic stimuli while maintaining remarkable structural stability and tightly regulated length. The mechanisms underlying this stability and length control are not well understood.
View Article and Find Full Text PDFAm J Physiol Renal Physiol
September 2025
Department II of Internal Medicine and Center for Molecular Medicine Cologne, University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Nephronophthisis (NPH) is an autosomal-recessive cystic kidney disease representing the most frequent genetic cause of end-stage kidney failure in children and adolescents. NPH is caused by genetic variants in >20 NPHP genes. Although nearly all NPHP genes encode ciliary proteins, classifying NPH as a renal ciliopathy, there is evidence for a pathogenic role of a compromised DNA damage response (DDR).
View Article and Find Full Text PDFbioRxiv
June 2025
Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Background: Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations affecting polycystin-1 (PC1) or -2 (PC2). The existence of a 'cilia-dependent cyst activation' (CDCA) pathway has been identified by demonstrating that structurally intact primary cilia are crucial for cyst growth following loss of polycystins. We previously used translating ribosome affinity purification (TRAP) RNA-Seq on pre-cystic mouse kidneys to determine the translatome that meet the criteria for CDCA and identified as an early effector of polycystin signaling.
View Article and Find Full Text PDFBio Protoc
May 2025
Department of Molecular and Cell Biology, University of California, Merced, Merced California, CA, USA.
Known as the cell's antenna and signaling hub, the primary cilium is a hair-like organelle with a few micrometers in length and 200-300 nm in diameter. Due to the small size of the primary cilium, it is technically challenging to profile ciliary proteins from mammalian cells. Traditional methods, such as physical isolation of cilia, are susceptible to contamination from other cellular components.
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