2017
Role of Primary Cilia in Odontogenesis
HAMPL, Marek, P. CELA, H.L. SZABO-ROGERS, Michaela BOSÁKOVÁ, H. DOSEDELOVA et. al.Základní údaje
Originální název
Role of Primary Cilia in Odontogenesis
Autoři
HAMPL, Marek (203 Česká republika, domácí), P. CELA (203 Česká republika), H.L. SZABO-ROGERS (840 Spojené státy), Michaela BOSÁKOVÁ (203 Česká republika), H. DOSEDELOVA (203 Česká republika), Pavel KREJČÍ (203 Česká republika, domácí) a marcela BUCHTOVÁ (203 Česká republika, garant, domácí)
Vydání
Journal of Dental Research, THOUSAND OAKS, CA USA, SAGE PUBLICATIONS INC, 2017, 0022-0345
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30208 Dentistry, oral surgery and medicine
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 5.383
Kód RIV
RIV/00216224:14310/17:00094911
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000406054800001
Klíčová slova anglicky
craniofacial anomalies; growth/development; mineralized tissue/development; odontoblast(s); oral pathology; signal transduction
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 4. 2018 14:17, Ing. Nicole Zrilić
Anotace
V originále
Primary cilium is a solitary organelle that emanates from the surface of most postmitotic mammalian cells and serves as a sensory organelle, transmitting the mechanical and chemical cues to the cell. Primary cilia are key coordinators of various signaling pathways during development and maintenance of tissue homeostasis. The emerging evidence implicates primary cilia function in tooth development. Primary cilia are located in the dental epithelium and mesenchyme at early stages of tooth development and later during cell differentiation and production of hard tissues. The cilia are present when interactions between both the epithelium and mesenchyme are required for normal morphogenesis. As the primary cilium coordinates several signaling pathways essential for odontogenesis, ciliary defects can interrupt the latter process. Genetic or experimental alterations of cilia function lead to various developmental defects, including supernumerary or missing teeth, enamel and dentin hypoplasia, or teeth crowding. Moreover, dental phenotypes are observed in ciliopathies, including Bardet-Biedl syndrome, Ellis-van Creveld syndrome, Weyers acrofacial dysostosis, cranioectodermal dysplasia, and oral-facial-digital syndrome, altogether demonstrating that primary cilia play a critical role in regulation of both the early odontogenesis and later differentiation of hard tissue-producing cells. Here, we summarize the current evidence for the localization of primary cilia in dental tissues and the impact of disrupted cilia signaling on tooth development in ciliopathies.
Návaznosti
GA17-14886S, projekt VaV |
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