Loss of primary cilia in late pituitary organogenesis does not cause endocrine dysfunction

Abstract

Cilia are finger‐like organelles protruding from the cell membrane, and dysfunction of cilia can cause human diseases called ciliopathies with a range of phenotypes. Some ciliopathies include pituitary phenotypes, and previous studies have shown a role for non‐motile primary cilia in pituitary organogenesis. In this study, we generated a pituitary gland‐conditional knockout of the ciliary basal body protein CEP164 to investigate the role of primary cilia in pituitary development and postnatal function. Our mouse model shows a loss of pituitary primary cilia between e14.5 and e18.5, although pituitary organogenesis and morphology appear normal in late embryos and postpubertal mice of both sexes. No physiological defects were noted in postpubertal mice, although there were minor changes in the expression of Sox2 and Prl transcripts. We conclude that primary cilia are dispensable in late pituitary organogenesis, therefore suggesting the role of primary cilia occurs during early pituitary development. Further studies may investigate whether cilia are required for specific responses to physiological or pathological conditions where endocrine needs are altered.