Notch regulation of progenitor cell behavior in quiescent and regenerating auditory epithelium of mature birds

被引:79
作者
Daudet, Nicolas [2 ,3 ]
Gibson, Robin [1 ]
Shang, Jialin
Bernard, Amy [1 ]
Lewis, Julian
Stone, Jennifer [1 ]
机构
[1] Univ Washington, Dept Otolaryngol Head & Neck Surg, Virginia Merrill Bloedel Hearing Res Ctr, Seattle, WA 98195 USA
[2] Canc Res UK, Vertebrate Dev Lab, London, England
[3] UCL, UCL Ear Inst, Ctr Auditory Res, London, England
基金
英国生物技术与生命科学研究理事会;
关键词
Notch; Lateral inhibition; Hair cell; Regeneration; Chicken; Transdifferentiation; Progenitor; AVIAN INNER-EAR; HAIR-CELLS; SENSORY EPITHELIA; ACOUSTIC TRAUMA; CHICK COCHLEA; DIRECT TRANSDIFFERENTIATION; PROSENSORY PATCHES; MAMMALIAN COCHLEA; SIGNALING PATHWAY; FATE CHOICES;
D O I
10.1016/j.ydbio.2008.10.033
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Unlike mammals, birds regenerate auditory hair cells (HCs) after injury. During regeneration, mature nonsensory supporting cells (SCs) leave quiescence and convert into HCs, through non-mitotic or mitotic mechanisms. During embryogenesis, Notch ligands from nascent HCs exert lateral inhibition, restricting HC production. Here, we examined whether Notch signaling (1) is needed in mature birds to maintain the HC/SC pattern in the undamaged auditory epithelium or (2) governs SC behavior once HCs are injured. We show that Notch pathway genes are transcribed in the mature undamaged epithelium, and after HC injury, their transcription is upregulated in the region of highest mitotic activity. In vitro treatment with DAFT, an inhibitor of Notch activity, had no effect on SCs in the undamaged epithelium. Following HC damage, DART had no direct effect on SC division. However, after damage, DAPT caused excessive regeneration of HCs at the expense of SCs, through both mitotic and non-mitotic mechanisms. Conversely, overexpression of activated Notch in SCs after damage caused them to maintain their phenotype and inhibited HC regeneration. Therefore, signaling through Notch is not required for SC quiescence in the healthy epithelium or to initiate HC regeneration after damage. Rather, Notch prevents SCs from regenerating excessive HCs after damage. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:86 / 100
页数:15
相关论文
共 67 条
[31]  
Kruger RP, 1999, J NEUROSCI, V19, P4815
[32]   Regulation of marginal zone B cell development by MINT, a suppressor of Notch/RBP-J signaling pathway [J].
Kuroda, K ;
Han, H ;
Tani, S ;
Tanigaki, K ;
Tun, T ;
Furukawa, T ;
Taniguchi, Y ;
Kurooka, H ;
Hamada, Y ;
Toyokuni, S ;
Honjo, T .
IMMUNITY, 2003, 18 (02) :301-312
[33]   Notch signalling pathway mediates hair cell development in mammalian cochlea [J].
Lanford, PJ ;
Lan, Y ;
Jiang, RL ;
Lindsell, C ;
Weinmaster, G ;
Gridley, T ;
Kelley, MW .
NATURE GENETICS, 1999, 21 (03) :289-292
[34]   Expression of Math1 and HES5 in the cochleae of wildtype and Jag2 mutant mice [J].
Lanford, RJ ;
Shailam, R ;
Norton, CR ;
Gridley, T ;
Kelley, MW .
JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY, 2000, 1 (02) :161-171
[35]   Expression of radical fringe in limb-bud ectoderm regulates apical ectodermal ridge formation [J].
Laufer, E ;
Dahn, R ;
Orozco, OE ;
Yeo, CY ;
Pisenti, J ;
Henrique, D ;
Abbott, UK ;
Fallon, JF ;
Tabin, C .
NATURE, 1997, 386 (6623) :366-373
[36]   Notch signalling and the control of cell fate choices in vertebrates [J].
Lewis, J .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1998, 9 (06) :583-589
[37]   Neurogenic genes and vertebrate neurogenesis [J].
Lewis, J .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (01) :3-10
[38]  
LEWIS J, 1991, REGENERATION VERTEBR, P103
[39]   Notch signaling regulates the extent of hair cell regeneration in the zebrafish lateral line [J].
Ma, Eva Y. ;
Rubel, Edwin W. ;
Raible, David W. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (09) :2261-2273
[40]   Zebrafish atoh1 genes:: classic proneural activity in the inner ear and regulation by Fgf and Notch [J].
Millimaki, Bonny B. ;
Sweet, Elly M. ;
Dhason, Mary S. ;
Riley, Bruce B. .
DEVELOPMENT, 2007, 134 (02) :295-305