Role of cilia in the pathogenesis of congenital heart disease

Semin Cell Dev Biol. 2021 Feb:110:2-10. doi: 10.1016/j.semcdb.2020.04.017. Epub 2020 May 14.

Abstract

An essential role for cilia in the pathogenesis of congenital heart disease (CHD) has emerged from findings of a large-scale mouse forward genetic screen. High throughput screening with fetal ultrasound imaging followed by whole exome sequencing analysis recovered a preponderance of cilia related genes and cilia transduced cell signaling genes among mutations identified to cause CHD. The perturbation of left-right patterning in CHD pathogenesis is suggested by the association of CHD with heterotaxy, but also by the finding of the co-occurrence of laterality defects with CHD in birth defect registries. Many of the cilia and cilia cell signaling genes recovered were found to be related to Hedgehog signaling. Studies in mice showed cilia transduced hedgehog signaling coordinates left-right patterning with heart looping and differentiation of the heart tube. Cilia transduced Shh signaling also regulates later events in heart development, including outflow tract septation and formation of the atrioventricular septum. More recent work has shown mutations in cilia related genes may also contribute to valve disease that largely manifest in adult life. Overall, these and other findings show cilia play an important role in CHD and also in more common valve diseases.

Keywords: Cilia; Congenital heart disease; Fetal ultrasound imaging; Forward genetics; Mouse models; Mutagenesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Body Patterning / genetics
  • Cilia / metabolism*
  • Cilia / pathology
  • Cilia / ultrastructure
  • Disease Models, Animal
  • Exome Sequencing
  • Fetus
  • Gene Expression Regulation
  • Heart Defects, Congenital / diagnostic imaging
  • Heart Defects, Congenital / genetics*
  • Heart Defects, Congenital / metabolism
  • Heart Defects, Congenital / pathology
  • Humans
  • Kinesins / genetics
  • Kinesins / metabolism
  • Low Density Lipoprotein Receptor-Related Protein-2 / genetics
  • Low Density Lipoprotein Receptor-Related Protein-2 / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Ultrasonography, Prenatal
  • Ventricular Septum / diagnostic imaging
  • Ventricular Septum / metabolism*
  • Ventricular Septum / pathology
  • Wnt Signaling Pathway / genetics*

Substances

  • Jbts17 protein, mouse
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Lrp2 protein, mouse
  • Membrane Proteins
  • Repressor Proteins
  • Sufu protein, mouse
  • Kif7 protein, mouse
  • Kinesins