Hufnagel Lars, Teleman Aurelio A, Rouault Hervé, Cohen Stephen M, Shraiman Boris I
Kavli Institute for Theoretical Physics, Kohn Hall, University of California-Santa Barbara, Santa Barbara, CA 93106, USA.
Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):3835-40. doi: 10.1073/pnas.0607134104. Epub 2007 Feb 28.
A fundamental and unresolved problem in animal development is the question of how a growing tissue knows when it has achieved its correct final size. A widely held view suggests that this process is controlled by morphogen gradients, which adapt to tissue size and become flatter as tissue grows, leading eventually to growth arrest. Here, we present evidence that the decapentaplegic (Dpp) morphogen distribution in the developing Drosophila wing imaginal disk does not adapt to disk size. We measure the distribution of a functional Dpp-GFP transgene and the Dpp signal transduced by phospho-Mad and show that the characteristic length scale of the Dpp profile remains approximately constant during growth. This finding suggests an alternative scenario of size determination, where disk size is determined relative to the fixed morphogen distribution by a certain threshold level of morphogen required for growth. We propose that when disk boundary reaches the threshold the arrest of cell proliferation throughout the disk is induced by mechanical stress in the tissue. Mechanical stress is expected to arise from the nonuniformity of morphogen distribution that drives growth. This stress, through a negative feedback on growth, can compensate for the nonuniformity of morphogen, achieving uniform growth with the rate that vanishes when disk boundary reaches the threshold. The mechanism is demonstrated through computer simulations of a tissue growth model that identifies the key assumptions and testable predictions. This analysis provides an alternative hypothesis for the size determination process. Novel experimental approaches will be needed to test this model.
动物发育中一个基本且尚未解决的问题是,正在生长的组织如何知道它何时达到了正确的最终大小。一种广泛持有的观点认为,这个过程由形态发生素梯度控制,形态发生素梯度会根据组织大小进行调整,并随着组织生长而变得更平缓,最终导致生长停滞。在此,我们提供证据表明,在发育中的果蝇翅成虫盘里,“驼背”(Dpp)形态发生素的分布并不随盘的大小而调整。我们测量了功能性Dpp-GFP转基因的分布以及由磷酸化Mad转导的Dpp信号,结果表明,在生长过程中,Dpp分布的特征长度尺度大致保持恒定。这一发现提示了一种大小确定的替代情形,即盘的大小是相对于固定的形态发生素分布,由生长所需的某个形态发生素阈值水平来确定的。我们提出,当盘边界达到该阈值时,整个盘中细胞增殖的停滞是由组织中的机械应力诱导的。机械应力预计源于驱动生长的形态发生素分布的不均匀性。这种应力通过对生长的负反馈,可以补偿形态发生素的不均匀性,以在盘边界达到阈值时速率消失的方式实现均匀生长。通过对一个组织生长模型的计算机模拟验证了该机制,该模拟确定了关键假设和可检验的预测。这一分析为大小确定过程提供了一个替代假说。需要新的实验方法来检验这个模型。