Dbx1-Expressing Cells Are Necessary for the Survival of the Mammalian Anterior Neural and Craniofacial Structures

被引:18
作者
Causeret, Frederic [1 ]
Ensini, Monica [1 ]
Teissier, Anne [1 ]
Kessaris, Nicoletta [2 ,3 ]
Richardson, William D. [2 ,3 ]
de Couville, Thibaut Lucas [1 ]
Pierani, Alessandra [1 ]
机构
[1] Univ Paris Diderot, Inst Jacques Monod, CNRS, UMR 7592, Paris, France
[2] UCL, Dept Cell & Dev Biol, London, England
[3] UCL, Wolfson Inst Biomed Res, London, England
来源
PLOS ONE | 2011年 / 6卷 / 04期
关键词
BRAIN-DEVELOPMENT; MOUSE EMBRYOS; SPINAL-CORD; CREST; FOREBRAIN; GENE; MORPHOGENESIS; EXPRESSION; MALFORMATION; RECOMBINASE;
D O I
10.1371/journal.pone.0019367
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Development of the vertebrate forebrain and craniofacial structures are intimately linked processes, the coordinated growth of these tissues being required to ensure normal head formation. In this study, we identify five small subsets of progenitors expressing the transcription factor dbx1 in the cephalic region of developing mouse embryos at E8.5. Using genetic tracing we show that dbx1-expressing cells and their progeny have a modest contribution to the forebrain and face tissues. However, their genetic ablation triggers extensive and non cell-autonomous apoptosis as well as a decrease in proliferation in surrounding tissues, resulting in the progressive loss of most of the forebrain and frontonasal structures. Targeted ablation of the different subsets reveals that the very first dbx1-expressing progenitors are critically required for the survival of anterior neural tissues, the production and/or migration of cephalic neural crest cells and, ultimately, forebrain formation. In addition, we find that the other subsets, generated at slightly later stages, each play a specific function during head development and that their coordinated activity is required for accurate craniofacial morphogenesis. Our results demonstrate that dbx1-expressing cells have a unique function during head development, notably by controlling cell survival in a non cell-autonomous manner.
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页数:13
相关论文
共 36 条
[1]   Multiple origins of Cajal-Retzius cells at the borders of the developing pallium [J].
Bielle, F ;
Griveau, A ;
Narboux-Nême, N ;
Vigneau, S ;
Sigrist, M ;
Arber, S ;
Wassef, M ;
Pierani, A .
NATURE NEUROSCIENCE, 2005, 8 (08) :1002-1012
[2]   Patterning the cerebral cortex: traveling with morphogens [J].
Borello, Ugo ;
Pierani, Alessandra .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2010, 20 (04) :408-415
[3]  
Brault V, 2001, DEVELOPMENT, V128, P1253
[4]  
Chai Y, 2000, DEVELOPMENT, V127, P1671
[5]   The genetic basis of mammalian neurulation [J].
Copp, AJ ;
Greene, NDE ;
Murdoch, JN .
NATURE REVIEWS GENETICS, 2003, 4 (10) :784-793
[6]   Reciprocal relationships between Fgf8 and neural crest cells in facial and forebrain development [J].
Creuzet, S ;
Schuler, B ;
Couly, G ;
Le Douarin, NM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4843-4847
[7]   The cephalic neural crest exerts a critical effect on forebrain and midbrain development [J].
Creuzet, Sophie E. ;
Martinez, Salvador ;
Le Douarin, Nicole M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (38) :14033-14038
[8]   Regulation of pre-otic brain development by the cephalic neural crest [J].
Creuzet, Sophie E. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (37) :15774-15779
[9]   Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase [J].
Danielian, PS ;
Muccino, D ;
Rowitch, DH ;
Michael, SK ;
McMahon, AP .
CURRENT BIOLOGY, 1998, 8 (24) :1323-1326
[10]  
Etchevers HC, 1999, DEVELOPMENT, V126, P3533