Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.
Cold Spring Harb Perspect Biol. 2009 Sep;1(3):a002493. doi: 10.1101/cshperspect.a002493.
During development, secreted morphogens such as Wnt, Hedgehog (Hh), and BMP emit from their producing cells in a morphogenetic field, and specify different cell fates in a direct concentration-dependent manner. Understanding how morphogens form their concentration gradients to pattern tissues has been a central issue in developmental biology. Various experimental studies from Drosophila have led to several models to explain the formation of morphogen gradients. Over the past decade, one of the main findings in this field is the characterization of heparan sulfate proteoglycan (HSPG) as an essential regulator for morphogen gradient formation. Genetic and cell biological studies have showed that HSPGs can regulate morphogen activities at various steps including control of morphogen movement, signaling, and intracellular trafficking. Here, we review these data, highlighting recent findings that reveal mechanistic roles of HSPGs in controlling morphogen gradient formation.
在发育过程中,分泌形态发生素,如 Wnt、Hedgehog(Hh)和 BMP,从其产生细胞中以形态发生场的形式发出,并以直接浓度依赖的方式特异性地决定不同的细胞命运。了解形态发生素如何形成浓度梯度来模式化组织一直是发育生物学的核心问题。来自果蝇的各种实验研究提出了几个模型来解释形态发生素梯度的形成。在过去的十年中,该领域的主要发现之一是将肝素硫酸蛋白聚糖(HSPG)鉴定为形态发生素梯度形成的必需调节剂。遗传和细胞生物学研究表明,HSPG 可以在包括控制形态发生素运动、信号转导和细胞内运输在内的各种步骤中调节形态发生素的活性。在这里,我们回顾这些数据,强调最近的发现,这些发现揭示了 HSPG 在控制形态发生素梯度形成中的机制作用。