Developmental biology and the redirection or replacement of cells

被引:1
作者
Gurdon, J
机构
[1] Wellcome CRC Inst, Cambridge CB2 1QR, England
[2] Univ Cambridge, Dept Zool, Cambridge CB2 1TN, England
基金
英国惠康基金;
关键词
cloning; nuclear transplantaion; stem cells; genome; ricin; Prometheus;
D O I
10.1098/rstb.1999.0536
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The aim of developmental biology is to understand how an egg converts itself into a complete organism through the processes of cell differentiation, morphogenesis and size regulation. The principles that have emerged over recent decades include the constancy of the genome in nearly all cells of an individual, the existence of stem cells in many organs and the overwhelming importance of signalling between cells for the determination of their fate. These and other characteristics of development are discussed here in relation to the prospect of achieving cell and tissue correction or replacement with thr help of nuclear transplantation and signalling factors. Nuclear transplantation offers a one-step procedure for generating multipotent embryo cells from the cells of an adult tissue such as skin. It should be possible to proliferate the resulting cells as carl be done for mouse embryonic stem cells. Embryo cells can be made to differentiate in many directions by exposing them to various agents or to different concentrations of a single factor such as the transforming growth factor beta class signalling molecule activin. The possibility of a cancerous condition being acquired during these experimental manipulations can be guarded against by transfecting cells with a conditional suicide gene. Thus it may be possible to generate replacement cells or tissues from an adult human for trans plantation back to the original donor, without the disadvantage of any genetic incompatibility.
引用
收藏
页码:1967 / 1976
页数:10
相关论文
共 28 条
[1]  
ANDREW C, 1991, KGB INSIDE STORY, P664
[2]   Amphibian limb regeneration: Rebuilding a complex structure [J].
Brockes, JP .
SCIENCE, 1997, 276 (5309) :81-87
[3]   Size control in animal development [J].
Conlon, I ;
Raff, M .
CELL, 1999, 96 (02) :235-244
[4]  
Davidson EH., 1986, GENE ACTIVITY EARLY
[5]   ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156
[6]  
Gilbert SF., 1997, DEV BIOL, V5th
[7]   Control of translation initiation in animals [J].
Gray, NK ;
Wickens, M .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :399-458
[8]   RESPONSES OF EMBRYONIC XENOPUS CELLS TO ACTIVIN AND FGF ARE SEPARATED BY MULTIPLE DOSE THRESHOLDS AND CORRESPOND TO DISTINCT AXES OF THE MESODERM [J].
GREEN, JBA ;
NEW, HV ;
SMITH, JC .
CELL, 1992, 71 (05) :731-739
[9]  
GURDON JB, 1986, J CELL SCI, P287
[10]  
HESIOD, THEOGONY, P523