β-连环蛋白/Wnt 信号通路控制斑马鱼发育和再生视网膜祖细胞的命运。
β-catenin/Wnt signaling controls progenitor fate in the developing and regenerating zebrafish retina.
机构信息
Department of Biology, Colgate University, Hamilton, NY 13346, USA.
出版信息
Neural Dev. 2012 Aug 24;7:30. doi: 10.1186/1749-8104-7-30.
BACKGROUND
The zebrafish retina maintains two populations of stem cells: first, the germinal zone or ciliary marginal zone (CMZ) contains multipotent retinal progenitors that add cells to the retinal periphery as the fish continue to grow; second, radial glia (Müller cells) occasionally divide asymmetrically to generate committed progenitors that differentiate into rod photoreceptors, which are added interstitially throughout the retina with growth. Retinal injury stimulates Müller glia to dedifferentiate, re-enter the cell cycle, and generate multipotent retinal progenitors similar to those in the CMZ to replace missing neurons. The specific signals that maintain these two distinct populations of endogenous retinal stem cells are not understood.
RESULTS
We used genetic and pharmacological manipulation of the β-catenin/Wnt signaling pathway to show that it is required to maintain proliferation in the CMZ and that hyperstimulation of β-catenin/Wnt signaling inhibits normal retinal differentiation and expands the population of proliferative retinal progenitors. To test whether similar effects occur during regeneration, we developed a method for making rapid, selective photoreceptor ablations in larval zebrafish with intense light. We found that dephosphorylated β-catenin accumulates in Müller glia as they re-enter the cell cycle following injury, but not in Müller glia that remain quiescent. Activation of Wnt signaling is required for regenerative proliferation, and hyperstimulation results in loss of Müller glia from the INL as all proliferative cells move into the ONL.
CONCLUSIONS
β-catenin/Wnt signaling is thus required for the maintenance of retinal progenitors during both initial development and lesion-induced regeneration, and is sufficient to prevent differentiation of those progenitors and maintain them in a proliferative state. This suggests that the β-catenin/Wnt cascade is part of the shared molecular circuitry that maintains retinal stem cells for both homeostatic growth and epimorphic regeneration.
背景
斑马鱼的视网膜维持着两种干细胞群体:首先,生发区或纤毛边缘区(CMZ)包含多能视网膜祖细胞,当鱼继续生长时,这些祖细胞会向视网膜边缘添加细胞;其次,放射状胶质细胞(Müller 细胞)偶尔不对称分裂,产生定向祖细胞,分化为杆状光感受器,这些光感受器在整个视网膜中随着生长而间质添加。视网膜损伤刺激 Müller 胶质细胞去分化,重新进入细胞周期,并产生类似于 CMZ 中的多能视网膜祖细胞,以替代缺失的神经元。维持这两种不同群体的内源性视网膜干细胞的特定信号尚未被理解。
结果
我们使用β-catenin/Wnt 信号通路的遗传和药理学操作来表明,它是维持 CMZ 增殖所必需的,并且过度刺激β-catenin/Wnt 信号会抑制正常的视网膜分化并扩大增殖性视网膜祖细胞的数量。为了测试在再生过程中是否会发生类似的影响,我们开发了一种在幼虫斑马鱼中快速、选择性地进行光感受器消融的方法,使用强光。我们发现,在损伤后 Müller 胶质细胞重新进入细胞周期时,磷酸化的β-catenin 会在 Müller 胶质细胞中积累,但在保持静止的 Müller 胶质细胞中不会积累。Wnt 信号的激活对于再生增殖是必需的,过度刺激会导致 Müller 胶质细胞从 INL 丢失,因为所有增殖细胞都移动到 ONL。
结论
因此,β-catenin/Wnt 信号在初始发育和损伤诱导的再生过程中维持视网膜祖细胞是必需的,足以防止这些祖细胞分化并使其保持增殖状态。这表明β-catenin/Wnt 级联反应是维持视网膜干细胞用于同源生长和胚胎再生的共享分子电路的一部分。