Home > B. Cellular pathology > motile cilia
motile cilia
Saturday 21 January 2006
The architecture of the microtubule backbone distinguishes motile cilia, in which nine doublets of microtubules surround a central pair (9+2), from primary cilia, in which the central pair of microtubules is absent (9+0).
Function
Motile cilia and flagella appeared very early in evolution to provide unicellular organisms with motility in water. Adaptation to non-aquatic life in plants resulted in the almost complete elimination of these organelles, except for gametic transport in some phylogenetic groups.
In contrast, cilia and flagella were retained and employed for a wide variety of functions requiring fluid movement in complex multicellular animals.
The function of the primary cilium as a highly conserved sensory organelle in evolution. The functions of cilia in diverse processes such as left-right axis pattern formation, cerebrospinal fluid flow, - sensory reception, mucociliary clearance and renal physiology indicate that cilia have been adapted as versatile tools for many biological processes.
Pathology
primary ciliary dyskinesia
- Kartagener syndrome
- situs inversus totalis (MIM.270100)
Bardet-Bield symdrome
ADPKD
See also: stereocilia
References
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Mykytyn K, Sheffield VC. Establishing a connection between cilia and Bardet-Biedl Syndrome. Trends Mol Med. 2004 Mar;10(3):106-9. PMID: 15106604
Ibanez-Tallon I, Heintz N, Omran H. To beat or not to beat: roles of cilia in development and disease. Hum Mol Genet. 2003 Apr 2;12(Suppl 1):R27-35. PMID: 12668594
El Zein L, Omran H, Bouvagnet P. Lateralization defects and ciliary dyskinesia: lessons from algae. Trends Genet. 2003 Mar;19(3):162-7. PMID: 12615011
Pazour GJ, Rosenbaum JL. Intraflagellar transport and cilia-dependent diseases. Trends Cell Biol. 2002 Dec;12(12):551-5. PMID: 12495842