Cilia Structure and Function in Human Disease.
Journal
Current opinion in endocrine and metabolic research
ISSN: 2451-9650
Titre abrégé: Curr Opin Endocr Metab Res
Pays: England
ID NLM: 101722894
Informations de publication
Date de publication:
Mar 2024
Mar 2024
Historique:
pmc-release:
01
03
2025
medline:
5
6
2024
pubmed:
5
6
2024
entrez:
5
6
2024
Statut:
ppublish
Résumé
Ciliary dysfunction causes a large group of developmental and degenerative human diseases known as ciliopathies. These diseases reflect the critical roles that cilia play in sensing the environment and in force generation for motility. Sensory functions include our senses of vision and olfaction. In addition, primary and motile cilia throughout our body monitor the environment allowing cells to coordinate their biology with the cells around them. This coordination is critical to organ development and maintenance, and ciliary dysfunction causes diverse structural birth defects and degenerative diseases. Defects in motility cause lung disease due to the failure of mucociliary clearance, male infertility due to the failure of sperm motility and the ability of sperm to move through the efferent ducts, and disturbances of the left-right axis due to a failure of nodal cilia to establish proper left-right cues.
Identifiants
pubmed: 38836197
doi: 10.1016/j.coemr.2024.100509
pmc: PMC11147146
pii:
doi:
Types de publication
Journal Article
Langues
eng
Déclaration de conflit d'intérêts
Declarations of interest: none.