Abstract
Our understanding of motile cilia and their role in disease has increased tremendously over the last two decades, with critical information and insight coming from the analysis of mouse models. Motile cilia form on specific epithelial cell types and typically beat in a coordinated, whip-like manner to facilitate the flow and clearance of fluids along the cell surface. Defects in formation and function of motile cilia result in primary ciliary dyskinesia (PCD), a genetically heterogeneous disorder with a well-characterized phenotype but no effective treatment. A number of model systems, ranging from unicellular eukaryotes to mammals, have provided information about the genetics, biochemistry, and structure of motile cilia. However, with remarkable resources available for genetic manipulation and developmental, pathological, and physiological analysis of phenotype, the mouse has risen to the forefront of understanding mammalian motile cilia and modeling PCD. This is evidenced by a large number of relevant mouse lines and an extensive body of genetic and phenotypic data. More recently, application of innovative cell biological techniques to these models has enabled substantial advancement in elucidating the molecular and cellular mechanisms underlying the biogenesis and function of mammalian motile cilia. In this article, we will review genetic and cell biological studies of motile cilia in mouse models and their contributions to our understanding of motile cilia and PCD pathogenesis.
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We gratefully thank Casey McKenzie for critical reading of the manuscript. This work was supported by Sanford Research (LL) and National Institutes of Health grant R01HL117836 from the National Heart, Lung, and Blood Institute (LEO).
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This work was supported by Sanford Research (LL) and National Institutes of Health grant R01HL117836 from the National Heart, Lung, and Blood Institute (LEO).
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Lee, L., Ostrowski, L.E. Motile cilia genetics and cell biology: big results from little mice. Cell. Mol. Life Sci. 78, 769–797 (2021). https://doi.org/10.1007/s00018-020-03633-5
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DOI: https://doi.org/10.1007/s00018-020-03633-5