Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1991 Feb;138(2):341-7.

Ultrastructure of respiratory cilia of WIC-Hyd male rats. An animal model for human immotile cilia syndrome

Affiliations

Ultrastructure of respiratory cilia of WIC-Hyd male rats. An animal model for human immotile cilia syndrome

C Torikata et al. Am J Pathol. 1991 Feb.

Abstract

The WIC-Hyd rat is a mutant from the Csk: Wistar-Imamichi rat, with spontaneous hydrocephalus. In male rats, the hydrocephalus is severe and about one half of hydrocephalic male littermates possess situs inversus totalis. Ependymal cilia in these animals are immotile, and this defect is regarded as a mechanical cause of hydrocephalus. This paper presents the ultrastructural features of respiratory cilia in these rats in comparison with those in human immotile cilia syndrome. The respiratory cilia in these rats also are immotile and the dynein arms are missing, as in human cases. Previously only eight dogs with immotile cilia syndrome and a mutant hydrocephalic-polydactyl mouse were reported with respect to these phenomena. However the WIC-Hyd rat is the first useful animal model for human immotile cilia syndrome, and further studies may serve to clarify the genetic background of this condition.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Pathol. 1973 Jan;109(1):75-8 - PubMed
    1. J Ultrastruct Mol Struct Res. 1988 Nov-Dec;101(2-3):210-4 - PubMed
    1. J Ultrastruct Res. 1974 Aug;48(2):242-58 - PubMed
    1. J Cell Biol. 1973 Nov;59(2 Pt 1):267-75 - PubMed
    1. J Cell Biol. 1975 Apr;65(1):227-33 - PubMed

LinkOut - more resources