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Publication : Mice with a Deletion of <i>Rsph1</i> Exhibit a Low Level of Mucociliary Clearance and Develop a Primary Ciliary Dyskinesia Phenotype.

First Author  Yin W Year  2019
Journal  Am J Respir Cell Mol Biol Volume  61
Issue  3 Pages  312-321
PubMed ID  30896965 Mgi Jnum  J:295985
Mgi Id  MGI:6455524 Doi  10.1165/rcmb.2017-0387OC
Citation  Yin W, et al. (2019) Mice with a Deletion of Rsph1 Exhibit a Low Level of Mucociliary Clearance and Develop a Primary Ciliary Dyskinesia Phenotype. Am J Respir Cell Mol Biol 61(3):312-321
abstractText  Primary ciliary dyskinesia (PCD) is a genetically and phenotypically heterogeneous disease caused by mutations in over 40 different genes. Individuals with PCD caused by mutations in RSPH1 (radial spoke head 1 homolog) have been reported to have a milder phenotype than other individuals with PCD, as evidenced by a lower incidence of neonatal respiratory distress, higher nasal nitric oxide concentrations, and better lung function. To better understand genotype-phenotype relationships in PCD, we have characterized a mutant mouse model with a deletion of Rsph1. Approximately 50% of cilia from Rsph1(-/-) cells appeared normal by transmission EM, whereas the remaining cilia revealed a range of defects, primarily transpositions or a missing central pair. Ciliary beat frequency in Rsph1(-/-) cells was significantly lower than in control cells (20.2 +/- 0.8 vs. 25.0 +/- 0.9 Hz), and the cilia exhibited an aberrant rotational waveform. Young Rsph1(-/-) animals demonstrated a low rate of mucociliary clearance in the nasopharynx that was reduced to zero by about 1 month of age. Rsph1(-/-) animals accumulated mucus in the nasal cavity but had a lower bacterial burden than animals with a deletion of dynein axonemal intermediate chain 1 (Dnaic1(-/-)). Thus, Rsph1(-/-) mice display a PCD phenotype similar to but less severe than that observed in Dnaic1(-/-) mice, similar to what has been observed in humans. The results suggest that some individuals with PCD may not have a complete loss of mucociliary clearance and further suggest that early diagnosis and intervention may be important to maintain this low amount of clearance.
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