Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency

• Published in: The journal of clinical endocrinology and metabolism 2020-09, Vol.105 (9), p.e3183-e3196
• Main Authors: Hamdi-Rozé, Houda, Ware, Michelle, Guyodo, Hélène, Rizzo, Aurélie, Ratié, Leslie, Rupin, Maïlys, Carré, Wilfrid, Kim, Artem, Odent, Sylvie, Dubourg, Christèle, David, Véronique, de Tayrac, Marie, Dupé, Valérie
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Brain; Cells, Cultured; Chick Embryo; Cohort Studies; Disease Models, Animal; Embryo, Mammalian; Endocrinology and metabolism; Female; Forebrain; Genetic variability; Haploinsufficiency; Haploinsufficiency - genetics; Hedgehog protein; Hedgehog Proteins - genetics; Hedgehog Proteins - metabolism; Holoprosencephaly; Holoprosencephaly - genetics; Holoprosencephaly - metabolism; Holoprosencephaly - pathology; Holoprosencephaly - physiopathology; Human health and pathology; Humans; Hypopituitarism; Hypothalamo-Hypophyseal System - metabolism; Hypothalamo-Hypophyseal System - pathology; Hypothalamus (anterior); Life Sciences; Male; Mice; Mice, Transgenic; Molecular modelling; Pituitary; Pituitary gland; Pregnancy; Receptors, Notch - deficiency; Receptors, Notch - genetics; Retrospective Studies; Signal transduction; Signal Transduction - genetics
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/clinem/dgaa249

In human, Sonic hedgehog (SHH) haploinsufficiency is the predominant cause of holoprosencephaly, a structural malformation of the forebrain midline characterized by phenotypic heterogeneity and incomplete penetrance. The NOTCH signaling pathway has recently been associated with holoprosencephaly in humans, but the precise mechanism involving NOTCH signaling during early brain development remains unknown. The aim of this study was to evaluate the relationship between SHH and NOTCH signaling to determine the mechanism by which NOTCH dysfunction could cause midline malformations of the forebrain. In this study, we have used a chemical inhibition approach in the chick model and a genetic approach in the mouse model. We also reported results obtained from the clinical diagnosis of a cohort composed of 141 holoprosencephaly patients. We demonstrated that inhibition of NOTCH signaling in chick embryos as well as in mouse embryos induced a specific downregulation of SHH in the anterior hypothalamus. Our data in the mouse also revealed that the pituitary gland was the most sensitive tissue to Shh insufficiency and that haploinsufficiency of the SHH and NOTCH signaling pathways synergized to produce a malformed pituitary gland. Analysis of a large holoprosencephaly cohort revealed that some patients possessed multiple heterozygous mutations in several regulators of both pathways. These results provided new insights into molecular mechanisms underlying the extreme phenotypic variability observed in human holoprosencephaly. They showed how haploinsufficiency of the SHH and NOTCH activity could contribute to specific congenital hypopituitarism that was associated with a sella turcica defect.