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Irx1 regulates dental outer enamel epithelial and lung alveolar type II epithelial differentiation.

Authors :
Yu W
Li X
Eliason S
Romero-Bustillos M
Ries RJ
Cao H
Amendt BA
Source :
Developmental biology [Dev Biol] 2017 Sep 01; Vol. 429 (1), pp. 44-55. Date of Electronic Publication: 2017 Jul 23.
Publication Year :
2017

Abstract

The Iroquois genes (Irx) appear to regulate fundamental processes that lead to cell proliferation, differentiation, and maturation during development. In this report, the Iroquois homeobox 1 (Irx1) transcription factor was functionally disrupted using a LacZ insert and LacZ expression demonstrated stage-specific expression during embryogenesis. Irx1 is highly expressed in the brain, lung, digits, kidney, testis and developing teeth. Irx1 null mice are neonatal lethal and this lethality it due to pulmonary immaturity. Irx1 <superscript>-/-</superscript> mice show delayed lung maturation characterized by defective surfactant protein secretion and Irx1 marks a population of SP-C expressing alveolar type II cells. Irx1 is specifically expressed in the outer enamel epithelium (OEE), stellate reticulum (SR) and stratum intermedium (SI) layers of the developing tooth. Irx1 mediates dental epithelial cell differentiation in the lower incisors resulting in delayed growth of the lower incisors. Irx1 is specifically and temporally expressed during developmental stages and we have focused on lung and dental development in this report. Irx1+ cells are unique to the development of the incisor outer enamel epithelium, patterning of Lef-1+ and Sox2+ cells as well as a new marker for lung alveolar type II cells. Mechanistically, Irx1 regulates Foxj1 and Sox9 to control cell differentiation during development.<br /> (Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1095-564X
Volume :
429
Issue :
1
Database :
MEDLINE
Journal :
Developmental biology
Publication Type :
Academic Journal
Accession number :
28746823
Full Text :
https://doi.org/10.1016/j.ydbio.2017.07.011