In vivo cell biology:: following the zebrafish trend

被引:125
作者
Beis, D
Stainier, DYR
机构
[1] Univ Calif San Francisco, Inst Cardiovasc Res, Dept Biochem & Biophys, Program Genet & Human Genet, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Inst Cardiovasc Res, Dept Biochem & Biophys, Program Dev Biol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tcb.2005.12.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A deeper understanding of the mechanisms of cell behavior is essential if we want to comprehend how an organism develops and functions. Changes in cellular processes, including the orientation of cell divisions, cell shape, polarity, differentiation and migration, account for tissue rearrangements during development and homeostasis. The in vivo relevance of in vitro findings is being constantly debated and the need for in vivo systems becoming more pressing. The zebrafish (Danio rerio) might become the vertebrate system of choice for a wide spectrum of biological questions that need to be investigated in vivo at cellular and subcellular resolutions. Here, we discuss some recent studies in which the zebrafish was used to gain insight into cell-biological mechanisms. Although this model system has been predominantly appreciated for its amenability to forward genetics, current advances in imaging technology and an increasing number of transgenic lines are bringing it closer to its full potential.
引用
收藏
页码:105 / 112
页数:8
相关论文
共 66 条
[1]   A molecular pathway leading to endoderm formation in zebrafish [J].
Alexander, J ;
Stainier, DYR .
CURRENT BIOLOGY, 1999, 9 (20) :1147-1157
[2]   The T box transcription factor no tail in ciliated cells controls zebrafish left-right asymmetry [J].
Amack, JD ;
Yost, HJ .
CURRENT BIOLOGY, 2004, 14 (08) :685-690
[3]   Genetic and cellular analyses of zebrafish atrioventricular cushion and valve development [J].
Beis, D ;
Bartman, T ;
Jin, SW ;
Scott, IC ;
D'Amico, LA ;
Ober, EA ;
Verkade, H ;
Frantsve, J ;
Field, HA ;
Wehman, A ;
Baier, H ;
Tallafuss, A ;
Bally-Cuif, L ;
Chen, JN ;
Stainier, DYR ;
Jungblut, B .
DEVELOPMENT, 2005, 132 (18) :4193-4204
[4]   Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D [J].
Bolz, H ;
von Brederlow, B ;
Ramírez, A ;
Bryda, EC ;
Kutsche, K ;
Nothwang, HG ;
Seeliger, M ;
Cabrera, MDS ;
Vila, MC ;
Molina, OP ;
Gal, A ;
Kubisch, C .
NATURE GENETICS, 2001, 27 (01) :108-112
[5]   The zebrafish Nodal signal Squint functions as a morphogen [J].
Chen, Y ;
Schier, AF .
NATURE, 2001, 411 (6837) :607-610
[6]   Production of maternal-zygotic mutant zebrafish by germ-line replacement [J].
Ciruna, B ;
Weidinger, G ;
Knaut, H ;
Thisse, B ;
Thisse, C ;
Raz, E ;
Schier, AF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (23) :14919-14924
[7]   Asymmetric cell division in C-elegans:: Cortical polarity and spindle positioning [J].
Cowan, CR ;
Hyman, AA .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2004, 20 :427-453
[8]   Delta-Notch signalling controls commitment to a secretory fate in the zebrafish intestine [J].
Crosnier, C ;
Vargesson, N ;
Gschmeissner, S ;
Ariza-McNaughton, L ;
Morrison, A ;
Lewis, J .
DEVELOPMENT, 2005, 132 (05) :1093-1104
[9]   An integrin-dependent role of pouch endoderm in hyoid cartilage development [J].
Crump, JG ;
Swartz, ME ;
Kimmel, CB .
PLOS BIOLOGY, 2004, 2 (09) :1432-1445
[10]   In vivo time-lapse imaging of cell divisions during neurogenesis in the developing zebrafish retina [J].
Das, T ;
Payer, B ;
Cayouette, M ;
Harris, WA .
NEURON, 2003, 37 (04) :597-609