Bryant P J, Simpson P
Q Rev Biol. 1984 Dec;59(4):387-415. doi: 10.1086/414040.
The growth rate and final size of developing organs is controlled by organ-intrinsic mechanisms as well as by hormones and growth factors that originate outside the target organ. Recent work on Drosophila imagined discs and other regenerating systems has led to the conclusion that the intrinsic growth-control mechanism that controls regenerative growth depends on position-specific interactions between cells and their neighbors, and that these interactions also control pattern formation. According to this interpretation, local growth by cell proliferation is stimulated when cells with disparate positional information are confronted as a result of grafting or wound healing. This local growth leads to intercalation of cells with intervening positional values until the positional information discontinuity is eliminated. When all discontinuities have been eliminated from a positional field, growth stops. In this article we consider the possibility that organ growth during normal development may be controlled by an intercalation mechanism similar to that proposed for regenerative growth. Studies of imaginal disc growth are consistent with this suggestion, and in addition they show that the cell interactions thought to control growth are independent of cell lineage. Developing organs of vertebrates also show intrinsic growth-control mechanisms, as demonstrated by the execution of normal growth programs by immature organs that are transplanted to fully grown hosts or to hosts with genetically different growth parameters. Furthermore, these organ-intrinsic mechanisms also appear to be based on position-specific cell interactions, as suggested by the growth stimulation seen after partial extirpation or rearrangement by grafting. In organs of most adult vertebrates, the organ-intrinsic growth-control system seems to be suppressed as shown by the loss of regenerative ability, although it is clearly retained in the limbs, tails and other organs of salamanders. The clearest example of an extrinsic growth regulator is growth hormone, which plays a dominant role along with insulin-like growth factors, thyroid hormone and sex hormones in supporting the growth of bones and other organs in postnatal mammals. These hormones do not appear to regulate prenatal growth, but other hormones and insulin-like growth factors may be important prenatally. The importance of other growth factors in regulating organ growth in vivo remains to be established. It is argued that both intrinsic and extrinsic factors control organ growth, and that there may be important interactions between the two types of control during development.
发育中器官的生长速率和最终大小受器官内在机制以及源自靶器官之外的激素和生长因子控制。最近关于果蝇成虫盘和其他再生系统的研究得出结论,控制再生生长的内在生长控制机制取决于细胞与其邻居之间的位置特异性相互作用,并且这些相互作用也控制模式形成。根据这种解释,当由于移植或伤口愈合而使具有不同位置信息的细胞相遇时,细胞增殖引起的局部生长会受到刺激。这种局部生长导致具有中间位置值的细胞插入,直到位置信息的不连续性被消除。当位置场中的所有不连续性都被消除时,生长停止。在本文中,我们考虑了正常发育过程中器官生长可能受类似于再生生长所提出的插入机制控制的可能性。对成虫盘生长的研究与这一观点一致,并进一步表明,被认为控制生长的细胞相互作用独立于细胞谱系。脊椎动物的发育器官也显示出内在生长控制机制,这一点已通过将未成熟器官移植到完全成熟的宿主或具有不同遗传生长参数的宿主中时正常生长程序的执行得到证明。此外,这些器官内在机制似乎也基于位置特异性细胞相互作用,这一点从部分切除或移植重排后观察到的生长刺激可以看出。在大多数成年脊椎动物的器官中,器官内在生长控制系统似乎因再生能力的丧失而受到抑制,尽管在蝾螈的四肢、尾巴和其他器官中显然保留了该系统。外在生长调节因子最明显的例子是生长激素,它与胰岛素样生长因子、甲状腺激素和性激素一起在支持出生后哺乳动物骨骼和其他器官的生长中起主导作用。这些激素似乎不调节产前生长,但其他激素和胰岛素样生长因子在产前可能很重要。其他生长因子在体内调节器官生长中的重要性仍有待确定。有人认为,内在和外在因素都控制器官生长,并且在发育过程中这两种控制类型之间可能存在重要的相互作用。