Boyle Scott, de Caestecker Mark
Nephrology Division and Department of Cell and Developmental Biology, Vanderbilt University, 1161 21st St. South S3223, Medical Ctr. North, Nashville, TN 37232, USA.
Am J Physiol Renal Physiol. 2006 Jul;291(1):F1-8. doi: 10.1152/ajprenal.00447.2005.
Many of the signaling pathways that regulate tissue specification and coordinate cellular differentiation during embryogenesis have been identified over the last decade. These pathways are integrated at the transcriptional level, enabling activation of specific developmental programs in a temporally and spatially restricted fashion. Such developmental events are usually thought of in terms of hierarchical relationships, in which the expression of upstream factors leads to the sequential activation of a linear cascade of downstream genes. Whereas these models provide a simplistic approach to understand complex cellular events, genetic and biochemical studies in mice and other model organisms provide ample evidence that many of these factors interact at multiple levels in vivo and emphasize the importance of considering these linear events in context. The purpose of this review is to emphasize the complexity of these regulatory networks during the early phases of mammalian kidney development, outlining some of the limitations and alternative approaches that are being used to explore the complex nature of these networks in vivo. Before describing these networks in detail, we will provide a brief overview of the main structural changes and tissue interactions involved in mammalian kidney development, and go on to describe some of the limitations of our current approaches to evaluate the role of these developmental pathways in vivo.
在过去十年中,已经确定了许多在胚胎发育过程中调节组织特化和协调细胞分化的信号通路。这些通路在转录水平上整合,能够以时间和空间受限的方式激活特定的发育程序。此类发育事件通常按照层级关系来考虑,其中上游因子的表达会导致下游基因线性级联的顺序激活。虽然这些模型为理解复杂的细胞事件提供了一种简单的方法,但在小鼠和其他模式生物中的遗传学和生物化学研究提供了充分的证据,表明这些因子中的许多在体内会在多个层面相互作用,并强调了在实际情况中考虑这些线性事件的重要性。本综述的目的是强调哺乳动物肾脏发育早期这些调控网络的复杂性,概述一些用于在体内探索这些网络复杂性质的局限性和替代方法。在详细描述这些网络之前,我们将简要概述哺乳动物肾脏发育中涉及的主要结构变化和组织相互作用,并继续描述我们目前在体内评估这些发育通路作用的方法的一些局限性。