- Ciliopathy
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Ciliopathy Classification and external resources 
Eukaryotic ciliumDiseasesDB 29887 MeSH D002925 A ciliopathy is a genetic disorder of the cellular cilia or the cilia anchoring structures, the basal bodies,[1] or of ciliary function.[2]
Although ciliopathies are usually considered to involve proteins that localize to the primary cilia or centrosomes, it is possible for ciliopathies to be associated with proteins such as XPNPEP3, which localizes to mitochondria but is believed to affect ciliiary function through proteolytic cleavage of ciliary proteins.[3]
Significant advances in understanding the importance of cilia were made beginning in the mid-1990s. However, "the physiological role that this organelle plays in most tissues remains elusive." Addition study of "how ciliary dysfunction can lead to such severe disease and developmental pathologies" is a subject of current research.[4]
Contents
History
Although non-motile or primary cilia were first described in 1898, "cell biologists largely ignored them." But "microscopists continued to document their presence in the cells of most vertebrate organisms." The "primary cilium was long considered--with few exceptions--to be a largely useless evolutionary vestige, a vestigial organelle. Recent research has revealed an initial understanding that cilia are essential to many of the body's organs"[5]. Many mammalian eukaryotic cells are ciliated with primary cilia. These primary cilia play important roles in chemosensation, mechanosensation, and thermosensation. Cilia may thus be "viewed as sensory cellular antennae that coordinate a large number of cellular signaling pathways, sometimes coupling the signaling to ciliary motility or alternatively to cell division and differentiation."[6]
Recent advances in mammalian genetic research have facilitated the elucidation of a molecular basis for a number of dysfunctional mechanisms in both motile and primary cilia structures of the cell.[7] "Numerous critical developmental signaling pathways" essential to cellular development have been discovered. These are principally but not exclusively found in the non-motile or primary cilia. A number of common observable characteristics of mammalian genetic disorders and diseases are caused by ciliary dysgenesis and dysfunction. Once identified, these characteristics thus describe a set of hallmarks of a ciliopathy[8].
Cilia have recently been implicated in a wide variety of human genetic diseases by "the discovery that numerous proteins involved in mammalian disease localize to the basal bodies and cilia." For example, in just a single area of human disease physiology, cystic renal disease, cilia-related genes and proteins have been identified to have causal effect in polycystic kidney disease, nephronophthisis, Senior-Loken syndrome type 5, orofaciodigital syndrome type 1 and Bardet-Biedl syndrome[4].
The mechanism of ciliary function
"In effect, the [motile cilium] is a nanomachine composed of perhaps over 600 proteins in molecular complexes, many of which also function independently as nanomachines." Cilia "function as mechano- or chemosensors and as a cellular global positioning system to detect changes in the surrounding environment." For example, ciliary signaling plays a role in the initiation of cellular replacement after cell damage.[6]
In addition to this sensory role mediating specific signaling cues, cilia play "a secretory role in which a soluble protein is released to have an effect downstream of the fluid flow" in epithelial cells, and can of course mediate fluid flow directly in the case of motile cilia.[1] Primary cilia in the retina play a role in transferring nourishment to the non-vascularized rod and cone cells from the vascularized cells several micrometres behind the surface of the retina.
Signal transduction pathways involved include the Hedgehog signaling pathway and the Wnt signaling pathway.[9]
Similar genes can result in a range of different diseases
"Just as different genes can contribute to similar diseases, so the same genes and families of genes can play a part in a range of different diseases." For example, in just two of the diseases caused by malfunctioning cilia, Meckel-Gruber syndrome and Bardet-Biedl syndrome, patients who carry mutations in genes associated with both diseases "have unique symptoms that are not seen in either condition alone." The genes linked to the two different conditions "interact with each other during development." Systems biologists are endeavoring to define functional modules containing multiple genes and then look at disorders whose phenotypes fit into such modules.[10]
A particular phenotype can overlap "considerably with several conditions (ciliopathies) in which primary cilia are also implicated in pathogenicity. One emerging aspect is the wide spectrum of ciliopathy gene mutations found within different diseases."[11]
Ciliopathies
"The phenotypic parameters that define a ciliopathy may be used to both recognize the cellular basis of a number of genetic disorders and to facilitate the diagnosis and treatment of some diseases of unknown etiology"[8].
Condition OMIM Gene(s) Systems/organs Alstrom syndrome[8],[1] 203800 ALMS1 Bardet-Biedl syndrome[8],[4][11] 209900 BBS1, BBS2, ARL6, BBS4, BBS5, MKKS, BBS7, TTC8, BBS9, BBS10, TRIM32, BBS12 Joubert syndrome[8][11] 213300 INPP5E, TMEM216, AHI1, NPHP1, CEP290, TMEM67, RPGRIP1L, ARL13B, CC2D2A, BRCC3 brain Meckel-Gruber syndrome[8][11][12] 249000 MKS1, TMEM67, TMEM216, CEP290, RPGRIP1L, CC2D2A liver, heart, bone nephronophthisis[8],[4][11] 256100 NPHP1, INVS, NPHP3, NPHP4, IQCB1, CEP290, GLIS2, RPGRIP1L kidney orofaciodigital syndrome 1[4][1] 311200 OFD1 Senior-Loken syndrome[4] 266900 NPHP1, NPHP4, IQCB1, CEP290, SDCCAG8 eye polycystic kidney disease[8],[4] (ADPKD and ARPKD)[13] 173900 PKD1, PKD2, PKHD1 kidney primary ciliary dyskinesia[8] 244400 DNAI1, DNAH5, TXNDC3, DNAH11, DNAI2, KTU, RSPH4A, RSPH9, LRRC50 asphyxiating thoracic dysplasia (Jeune)[8][verification needed] 208500 Marden-Walker syndrome[8][verification needed] 248700 situs inversus/Isomerism[8][verification needed] 270100 Other identified ciliopathies
- early embryonic death (some cases)[8]
- hydrocephalus (some cases)[8]
- polycystic liver disease[8]
- retinal degeneration (some forms)[8]
Implied or suspected ciliopathies
- agenesis of the corpus callosum[8]
- anencephaly[8]
- breathing abnomalities[8]
- cerebellar vermis hypoplasia[8]
- Dandy-Walker malformation[8]
- diabetes[8]
- Ellis-van Creveld syndrome[8]
- exencephaly[8]
- eye movement abnormalities[8]
- liver disease[8]
- hypoplasia of the corpus callosum[8]
- hypotonia[8]
- reproductive sterility[8]
- Jeune asphyxiating thoracic dystrophy[8]
- Juvenile myoclonic epilepsy (JME) [14]
- Kartagener syndrome[8]
- Marden-Walker syndrome[8]
- "mental retardation/developmental delay" or "other cognitive defects"[8]
- obesity[8][11]
- polydactyly[8]
- posterior encephalocele[8]
- respiratory dysfunction[8]
- "recurrent respiratory infections"[8]
- renal cystic disease[8]
- retinitis pigmentosa (some forms)[8][15]
- sensorineural deafness[8]
- situs inversus/Isomerism[8]
- spina bifida[8]
Clinical symptoms and ciliary roles
A wide variety of symptoms are potential clinical features of ciliopathy.
- Chemosensation abnormalities,[16], typically via ciliated epithelial cellular dysfunction.[1]
- Defective thermosensation or mechanosensation[17], often via ciliated epithelial cellular dysfunction.[1]
- Cellular motility dysfunction[16]
- Issues with displacement of extracellular fluid[16]
- Paracrine signal transduction abnormalities[16][1]
In organisms of normal health, cilia are critical for:
References
- ^ a b c d e f g Adams, M; UM Smith, CV Logan, CA Johnson (2008). "Recent advances in the molecular pathology, cell biology and genetics of ciliopathies". Journal of Medical Genetics (BMJ) 45 (5): 257–267. doi:10.1136/jmg. PMID 18178628. http://jmg.bmj.com/cgi/content/abstract/45/5/257. Retrieved 2009-08-20.
- ^ Lee JH, Gleeson JG (May 2010). "The role of primary cilia in neuronal function". Neurobiol. Dis. 38 (2): 167–72. doi:10.1016/j.nbd.2009.12.022. PMC 2953617. PMID 20097287. http://linkinghub.elsevier.com/retrieve/pii/S0969-9961(09)00377-5.
- ^ Hurd TW, Hildebrandt F (2011). "Mechanisms of Nephronophthisis and Related Ciliopathies". Nephron Exp. Nephrol. 118 (1): e9–e14. doi:10.1159/000320888. PMC 2992643. PMID 21071979. http://content.karger.com/produktedb/produkte.asp?typ=fulltext&file=000320888.
- ^ a b c d e f g Davenport JR, Yoder BK (2005). "An incredible decade for the primary cilium: a look at a once-forgotten organelle". Am. J. Physiol. Renal Physiol. 289 (6): F1159–69. doi:10.1152/ajprenal.00118.2005. PMID 16275743. http://ajprenal.physiology.org/cgi/content/abstract/289/6/F1159.
- ^ Gardiner, Mary Beth (September 2005). "The Importance of Being Cilia". HHMI Bulletin (Howard Hughes Medical Institute) 18 (2). http://www.hhmi.org/bulletin/sept2005/features/cilia.html. Retrieved 2008-07-26.
- ^ a b Satir, Peter; Søren T. Christensen (2008-03-26). "Structure and function of mammalian cilia". Histochemistry and Cell Biology (Springer Berlin / Heidelberg) 129 (6): 687–693. doi:10.1007/s00418-008-0416-9. PMC 2386530. PMID 18365235. 1432-119X. http://www.springerlink.com/content/x5051hq648t3152q/. Retrieved 2009-09-12.
- ^ Lancaster MA, Gleeson JG (June 2009). "The primary cilium as a cellular signaling center: lessons from disease". Curr. Opin. Genet. Dev. 19 (3): 220–9. doi:10.1016/j.gde.2009.04.008. PMC 2953615. PMID 19477114. http://linkinghub.elsevier.com/retrieve/pii/S0959-437X(09)00086-0.
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq Badano JL, Mitsuma N, Beales PL, Katsanis N (2006). "The ciliopathies: an emerging class of human genetic disorders". Annu Rev Genomics Hum Genet 7: 125–48. doi:10.1146/annurev.genom.7.080505.115610. PMID 16722803. http://arjournals.annualreviews.org/doi/abs/10.1146/annurev.genom.7.080505.115610.
- ^ D'Angelo A, Franco B (2009). "The dynamic cilium in human diseases". Pathogenetics 2 (1): 3. doi:10.1186/1755-8417-2-3. PMC 2694804. PMID 19439065. http://www.pathogeneticsjournal.com/content/2/1/3.
- ^ Hayden EC (2008). "Biological tools revamp disease classification" (Scholar search). Nature 453 (7196): 709. doi:10.1038/453709a. PMID 18528360. http://www.nature.com/news/2008/080604/full/453709a.html.
- ^ a b c d e f Ross, Allison; PL Beales, J Hill (2008). The Clinical, Molecular, and Functional Genetics of Bardet-Biedl Syndrome, in Genetics of Obesity Syndromes. Oxford University Press. pp. 177. ISBN 978-0-19-530016-1. http://books.google.com/?id=SOvEYxO2V4AC&dq. Retrieved 2009-07-01.
- ^ Kyttälä, Mira (2006-05) (pdf). Identification of the Meckel Syndrome Gene (MKS1) Exposes a Novel Ciliopathy. National Public Health Institute, Helsinki. http://www.ktl.fi/attachments/suomi/julkaisut/julkaisusarja_a/2006/2006a05.pdf. Retrieved 2008-07-06.
- ^ Gunay-Aygun M (November 2009). "Liver and Kidney Disease in Ciliopathies". Am J Med Genet C Semin Med Genet 151C (4): 296–306. doi:10.1002/ajmg.c.30225. PMC 2919058. PMID 19876928. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2919058.
- ^ Delgado-Escueta AV (2007). "Advances in Genetics of Juvenile Myoclonic Epilepsies". Epilepsy Curr 7 (3): 61–7. doi:10.1111/j.1535-7511.2007.00171.x. PMC 1874323. PMID 17520076. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1874323.
- ^ A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies, Nature Genetics 41, pp. 739-745, 2009-05, accessed 2010-11-24.
- ^ a b c d "Ciliary proteome database, v3". Database introduction. Johns Hopkins University. 2008. http://v3.ciliaproteome.org/cgi-bin/index.php. Retrieved 2009-01-07.
- ^ Tan PL, Barr T, Inglis PN, et al. (2007). "Loss of Bardet–Biedl syndrome proteins causes defects in peripheral sensory innervation and function". Proc. Natl. Acad. Sci. U.S.A. 104 (44): 17524–9. doi:10.1073/pnas.0706618104. PMC 2077289. PMID 17959775. http://www.pnas.org/content/104/44/17524.
- ^ a b c The Ciliary Proteome, Ciliaproteome V3.0 - Home Page, accessed 2010-06-11.
External links
- The Ciliary Proteome Web Page at Johns Hopkins
- Katsanis Lab, The Center for Human Disease Modeling, Duke University
- Ciliopathy Alliance UK - alliance of medical researchers, doctors and patient organisations representing patients and families suffering from ciliopathy diseases
- Deafness Research UK - genetics and hearing loss links, including ciliopathy conditions
Genetic disorder, organelle: Ciliopathy Structural receptor: Polycystic kidney disease
cargo: Asphyxiating thoracic dysplasia
basal body: Bardet–Biedl syndrome
mitotic spindle: Meckel syndrome
centrosome: Joubert syndromeSignaling Other/ungrouped Alström syndrome · Primary ciliary dyskinesia · Senior–Løken syndrome · Orofaciodigital syndrome 1 · McKusick–Kaufman syndrome · Autosomal recessive polycystic kidneyCategories:
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