Roignant Jean-Yves, Treisman Jessica E
Kimmel Center for Biology and Medicine of the Skirball Institute, New York University School of Medicine, Department of Cell Biology, New York, 10016, USA.
Int J Dev Biol. 2009;53(5-6):795-804. doi: 10.1387/ijdb.072483jr.
Differentiation of the Drosophila compound eye from the eye imaginal disc is a progressive process: columns of cells successively differentiate in a posterior to anterior sequence, clusters of cells form at regularly spaced intervals within each column, and individual photoreceptors differentiate in a defined order within each cluster. The progression of differentiation across the eye disc is driven by a positive autoregulatory loop of expression of the secreted molecule Hedgehog, which is temporally delayed by the intercalation of a second signal, Spitz. Hedgehog refines the spatial position at which each column initiates its differentiation by inducing secondary signals that act over different ranges to control the expression of positive and negative regulators. The position of clusters within each column is controlled by secreted inhibitory signals from clusters in the preceding column, and a single founder neuron, R8, is singled out within each cluster by Notch-mediated lateral inhibition. R8 then sequentially recruits surrounding cells to differentiate by producing a short-range signal, Spitz, which induces a secondary short-range signal, Delta. Intrinsic transcription factors act in combination with these two signals to produce cell-type diversity within the ommatidium. The Hedgehog and Spitz signals are transported along the photoreceptor axons and reused within the brain as long-range and local cues to trigger the differentiation and assembly of target neurons.
细胞柱以从后到前的顺序相继分化,细胞簇在每列中以规则间隔形成,并且单个光感受器在每个簇内按特定顺序分化。眼盘上分化的进程由分泌分子刺猬索尼克(Hedgehog)表达的正向自调节环驱动,该环被第二个信号斯皮茨(Spitz)的插入暂时延迟。刺猬索尼克通过诱导在不同范围内起作用以控制正负调节因子表达的次级信号,来细化每列开始分化的空间位置。每列内细胞簇的位置由前一列细胞簇分泌的抑制性信号控制,并且通过Notch介导的侧向抑制在每个簇内挑选出单个起始神经元R8。然后,R8通过产生短程信号斯皮茨来依次招募周围细胞进行分化,斯皮茨会诱导次级短程信号Delta。内在转录因子与这两个信号共同作用,在小眼内产生细胞类型多样性。刺猬索尼克和斯皮茨信号沿着光感受器轴突运输,并在大脑中作为长程和局部线索重新利用,以触发靶神经元的分化和组装。