Caenorhabditis elegans as a Model for Stem Cell Biology

被引:59
作者
Joshi, Pradeep M. [1 ]
Riddle, Misty R. [2 ]
Djabrayan, Nareg J. V. [2 ]
Rothman, Joel H. [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Mol Cell & Dev Biol, Santa Barbara, CA 93106 USA
关键词
stem cells; germline; reprogramming; transdifferentiation; microRNA; translational suppressors; TEMPORAL PATTERN-FORMATION; EMBRYONIC-GENE-ACTIVATION; DIRECTED RNA-POLYMERASE; GERM-LINE; SELF-RENEWAL; DEVELOPMENTAL PLASTICITY; CATENIN ASYMMETRY; BETA-CATENIN; SEAM CELL; DIFFERENTIATION;
D O I
10.1002/dvdy.22296
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We review the application of Caenorhabditis elegans as a model system to understand key aspects of stem cell biology. The only bona fide stem cells in C. elegans are those of the germline, which serves as a valuable paradigm for understanding how stem-cell niches influence maintenance and differentiation of stem cells and how somatic differentiation is repressed during germline development. Somatic cells that share stem cell-like characteristics also provide insights into principles in stem-cell biology. The epidermal seam cell lineages lend clues to conserved mechanisms of self-renewal and expansion divisions. Principles of developmental plasticity and reprogramming relevant to stem-cell biology arise from studies of natural transdifferentiation and from analysis of early embryonic progenitors, which undergo a dramatic transition from a pluripotent, reprogrammable condition to a state of committed differentiation. The relevance of these developmental processes to our understanding of stem-cell biology in other organisms is discussed. Developmental Dynamics 239:1539-1554, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:1539 / 1554
页数:16
相关论文
共 146 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   Starvation Protects Germline Stem Cells and Extends Reproductive Longevity in C-elegans [J].
Angelo, Giana ;
Van Gilst, Marc R. .
SCIENCE, 2009, 326 (5955) :954-958
[3]   C-elegans RNA-binding proteins PUF-8 and MEX-3 function redundantly to promote germline stem cell mitosis [J].
Ariz, Mohd ;
Mainpal, Rana ;
Subramaniam, Kuppuswarny .
DEVELOPMENTAL BIOLOGY, 2009, 326 (02) :295-304
[4]  
AUSTIN J, 1994, DEVELOPMENT, V120, P313
[5]   GLP-1 IS REQUIRED IN THE GERM LINE FOR REGULATION OF THE DECISION BETWEEN MITOSIS AND MEIOSIS IN C-ELEGANS [J].
AUSTIN, J ;
KIMBLE, J .
CELL, 1987, 51 (04) :589-599
[6]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]   Composition and dynamics of the Caenorhabditis elegans early embryonic transcriptome [J].
Baugh, LR ;
Hill, AA ;
Slonim, DK ;
Brown, EL ;
Hunter, CP .
DEVELOPMENT, 2003, 130 (05) :889-900
[8]   Dicer is essential for mouse development [J].
Bernstein, E ;
Kim, SY ;
Carmell, MA ;
Murchison, EP ;
Alcorn, H ;
Li, MZ ;
Mills, AA ;
Elledge, SJ ;
Anderson, KV ;
Hannon, GJ .
NATURE GENETICS, 2003, 35 (03) :215-217
[9]  
Berry LW, 1997, DEVELOPMENT, V124, P925
[10]   Translational Repression of Cyclin E Prevents Precocious Mitosis and Embryonic Gene Activation during C. elegans Meiosis [J].
Biedermann, Bjoern ;
Wright, Jane ;
Senften, Mathias ;
Kalchhauser, Irene ;
Sarathy, Gautham ;
Lee, Min-Ho ;
Ciosk, Rafal .
DEVELOPMENTAL CELL, 2009, 17 (03) :355-364