Matsuda Miho, Chitnis Ajay B
Laboratory of Molecular Genetics, Section on Neural Developmental Dynamics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Development. 2009 Jan;136(2):197-206. doi: 10.1242/dev.027938. Epub 2008 Dec 4.
Mind bomb1 (Mib1)-mediated endocytosis of the Notch ligand DeltaD is essential for activation of Notch in a neighboring cell. Although most DeltaD is localized in cytoplasmic puncta in zebrafish neural tissue, it is on the plasma membrane in mib1 mutants because Mib1-mediated endocytosis determines the normal subcellular localization of DeltaD. Knockdown of Notch increases cell surface DeltaA and DeltaD, but not DeltaC, suggesting that, like Mib1, Notch regulates endocytosis of specific ligands. Transplant experiments show that the interaction with Notch, both in the same cell (in cis) and in neighboring cells (in trans), regulates DeltaD endocytosis. Whereas DeltaD endocytosis following interaction in trans activates Notch in a neighboring cell, endocytosis of DeltaD and Notch following an interaction in cis is likely to inhibit Notch signaling by making both unavailable at the cell surface. The transplantation experiments reveal a heterogeneous population of progenitors: in some, cis interactions are more important; in others, trans interactions are more important; and in others, both cis and trans interactions are likely to contribute to DeltaD endocytosis. We suggest that this heterogeneity represents the process by which effective lateral inhibition leads to diversification of progenitors into cells that become specialized to deliver or receive Delta signals, where trans and cis interactions with Notch play differential roles in DeltaD endocytosis.
Mind bomb1(Mib1)介导的Notch配体DeltaD的内吞作用对于相邻细胞中Notch的激活至关重要。尽管大多数DeltaD定位于斑马鱼神经组织的细胞质点状结构中,但在mib1突变体中它位于质膜上,因为Mib1介导的内吞作用决定了DeltaD正常的亚细胞定位。Notch的敲低增加了细胞表面的DeltaA和DeltaD,但不影响DeltaC,这表明与Mib1一样,Notch调节特定配体的内吞作用。移植实验表明,在同一细胞内(顺式)和相邻细胞间(反式)与Notch的相互作用均调节DeltaD的内吞作用。反式相互作用后DeltaD的内吞作用会激活相邻细胞中的Notch,而顺式相互作用后DeltaD和Notch的内吞作用可能会通过使两者在细胞表面均不可用来抑制Notch信号传导。移植实验揭示了祖细胞群体的异质性:在一些祖细胞中,顺式相互作用更重要;在另一些中,反式相互作用更重要;还有一些中,顺式和反式相互作用可能都对DeltaD的内吞作用有贡献。我们认为这种异质性代表了有效侧向抑制导致祖细胞分化为专门传递或接收Delta信号的细胞的过程,其中与Notch的反式和顺式相互作用在DeltaD内吞作用中发挥不同作用。