RRC ID 11832
Author Kita A, Imayoshi I, Hojo M, Kitagawa M, Kokubu H, Ohsawa R, Ohtsuka T, Kageyama R, Hashimoto N.
Title Hes1 and Hes5 control the progenitor pool, intermediate lobe specification, and posterior lobe formation in the pituitary development.
Journal Mol. Endocrinol.
Abstract The pituitary gland is composed of two distinct entities: the adenohypophysis, including the anterior and intermediate lobes, and the neurohypophysis, known as the posterior lobe. This critical endocrine organ is essential for homeostasis, metabolism, reproduction, and growth. The pituitary development requires the control of proliferation and differentiation of progenitor cells. Although multiple signaling molecules and transcription factors are required for the proper pituitary development, the mechanisms that regulate the fate of progenitor cells remain to be elucidated. Hes genes, known as Notch effectors, play a crucial role in specifying cellular fates during the development of various tissues and organs. Here, we report that mice deficient for Hes1 and Hes5 display severe pituitary hypoplasia caused by accelerated differentiation of progenitor cells. In addition, this hypoplastic pituitary gland (adenohypophysis) lacks the intermediate lobe and exhibits the features of the anterior lobe only. Hes1 and Hes5 double-mutant mice also lack the neurohypophysis (the posterior lobe), probably due to incomplete evagination of the diencephalon. Thus, Hes genes control not only maintenance of progenitor cells but also intermediate vs. anterior lobe specification during the adenohypophysis development. Hes genes are also essential for the formation of the neurohypophysis.
Volume 21(6)
Pages 1458-66
Published 2007-6
DOI 10.1210/me.2007-0039
PII me.2007-0039
PMID 17426285
MeSH Animals Basic Helix-Loop-Helix Transcription Factors / analysis Basic Helix-Loop-Helix Transcription Factors / genetics Basic Helix-Loop-Helix Transcription Factors / metabolism* Cell Differentiation / genetics Homeodomain Proteins / analysis Homeodomain Proteins / genetics Homeodomain Proteins / metabolism* Mice Mice, Mutant Strains Organogenesis / genetics* Pituitary Gland, Posterior / abnormalities* Pituitary Gland, Posterior / growth & development* Pituitary Gland, Posterior / metabolism Repressor Proteins / analysis Repressor Proteins / genetics Repressor Proteins / metabolism* Stem Cells / cytology Stem Cells / metabolism Stem Cells / physiology* Transcription Factor HES-1
IF 3.678
Times Cited 58
WOS Category ENDOCRINOLOGY & METABOLISM
Resource
Mice Emx1-Cre