Hey2 Regulation by FGF Provides a Notch-Independent Mechanism for Maintaining Pillar Cell Fate in the Organ of Corti

被引:235
作者
Doetzlhofer, Angelika [1 ]
Basch, Martin L. [1 ]
Ohyama, Takahiro [1 ]
Gessler, Manfred [3 ]
Groves, Andrew K. [1 ,2 ]
Segil, Neil [1 ,2 ]
机构
[1] House Ear Res Inst, Gonda Dept Cell & Mol Biol, Los Angeles, CA 90057 USA
[2] Univ So Calif, Keck Sch Med, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
[3] Univ Wurzburg, Bioctr, Dept Physiol Chem 1, D-97074 Wurzburg, Germany
基金
美国国家卫生研究院;
关键词
CHICK INNER-EAR; GAMMA-SECRETASE; HAIR-CELLS; INTRAMEMBRANE PROTEOLYSIS; COCHLEAR DEVELOPMENT; VASCULAR DEVELOPMENT; PROSENSORY PATCHES; MAMMALIAN COCHLEA; SIGNALING PATHWAY; GENE-EXPRESSION;
D O I
10.1016/j.devcel.2008.11.008
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The organ of Corti, the auditory organ of the inner ear, contains two types of sensory hair cells and at least seven types of supporting cells. Most of these supporting cell types rely on Notch-dependent expression of Hes/Hey transcription factors to maintain the supporting cell fate. Here, we show that Notch signaling is not necessary for the differentiation and maintenance of pillar cell fate, that pillar cells are distinguished by Hey2 expression, and that-unlike other Hes/Hey factors-Hey2 expression is Notch independent. Hey2 is activated by FGF and blocks hair cell differentiation, whereas mutation of Hey2 leaves pillar cells sensitive to the loss of Notch signaling and allows them to differentiate as hair cells. We speculate that co-option of FGF signaling to render Hey2 Notch independent also liberated pillar cells from the need for direct contact with surrounding hair cells, and enabled evolutionary remodeling of the complex cellular mosaic of the inner ear.
引用
收藏
页码:58 / 69
页数:12
相关论文
共 65 条
[1]
Adam J, 1998, DEVELOPMENT, V125, P4645
[2]
Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[3]
From placode to polarization: new tunes in inner ear development [J].
Barald, KF ;
Kelley, MW .
DEVELOPMENT, 2004, 131 (17) :4119-4130
[4]
Math1:: An essential gene for the generation of inner ear hair cells [J].
Bermingham, NA ;
Hassan, BA ;
Price, SD ;
Vollrath, MA ;
Ben-Arie, N ;
Eatock, RA ;
Bellen, HJ ;
Lysakowski, A ;
Zoghbi, HY .
SCIENCE, 1999, 284 (5421) :1837-1841
[5]
Expression of Prox1 during mouse cochlear development [J].
Bermingham-McDonogh, O ;
Oesterle, EC ;
Stone, JS ;
Hume, CR ;
Huynh, HM ;
Hayashi, T .
JOURNAL OF COMPARATIVE NEUROLOGY, 2006, 496 (02) :172-186
[6]
Notch ligands with contrasting functions: Jagged1 and Delta1 in the mouse inner ear [J].
Brooker, R ;
Hozumi, K ;
Lewis, J .
DEVELOPMENT, 2006, 133 (07) :1277-1286
[7]
Chen P, 1999, DEVELOPMENT, V126, P1581
[8]
Notch2, but not Notch1, is required for proximal fate acquisition in the mammalian nephron [J].
Cheng, Hui-Teng ;
Kim, Mijin ;
Valerius, M. Todd ;
Surendran, Kameswaran ;
Schuster-Gossler, Karin ;
Gossler, Achim ;
McMahon, Andrew P. ;
Kopan, Raphael .
DEVELOPMENT, 2007, 134 (04) :801-811
[9]
Two contrasting roles for Notch activity in chick inner ear development: specification of prosensory patches and lateral inhibition of hair-cell differentiation [J].
Daudet, N ;
Lewis, J .
DEVELOPMENT, 2005, 132 (03) :541-551
[10]
Notch signalling is needed to maintain, but not to initiate, the formation of prosensory patches in the chick inner ear [J].
Daudet, Nicolas ;
Ariza-McNaughton, Linda ;
Lewis, Julian .
DEVELOPMENT, 2007, 134 (12) :2369-2378