| Literature DB >> 31205030 |
Bill Chaudhry, Deborah J Henderson.
Abstract
Motile cilia provide propulsion, and immotile ones are enriched with receptors. Both are required to establish left-right identity in the developing embryo and are also implicated in a wide range of human diseases. Abnormalities in cilial function underlie heterotaxy congenital heart disease (CHD) occurring in individuals with laterality disturbance. Mitochondrial function and cellular energetics, through mTOR and autophagy, are now linked with cilial function, revealing new mechanisms and candidate genes for syndromic human disease. In the current issue of the JCI, Burkhalter et al. ask the question: Can mitochondrial disturbances produce ciliopathy and does this explain some cases of heterotaxy?Entities:
Mesh:
Year: 2019 PMID: 31205030 PMCID: PMC6597205 DOI: 10.1172/JCI129827
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808