灵长类动物视网膜细胞发生的时空梯度。

D H Rapaport, P Rakic, M M LaVail
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引用次数: 0

摘要

在所有大脑结构的发育过程中,一个重要的事件是祖细胞离开细胞周期并开始分化的时间。我们用放射性胸腺嘧啶([3H]TdR)标记正在分裂的细胞,并利用它们在长时间存活后剩余的放射性标记,跟踪它们在分裂末期的命运,研究了猕猴(Macaca mulatta)视网膜中的细胞发生。观察到许多不同的细胞发生模式。视神经泡生成的视网膜色素上皮和神经视网膜这两种组织在时间和空间上具有密切一致的细胞发生模式,表明这一过程可能受到共同机制的控制。虽然在不同程度上重叠,但在神经视网膜内的特定细胞类型之间揭示了一个明确的发生顺序:首先产生神经节细胞,其次是水平细胞,锥状光感受器,无突细胞,m ller细胞,双极细胞,最后是杆状光感受器。不同体细胞直径的视网膜神经节细胞在不同的时间出生——最小的细胞产生得早,最大的细胞产生得晚,这表明猴子视网膜神经节细胞的功能分类有进一步的精细顺序(首先是P γ,然后是P β,最后是P α)。此外,在均匀的细胞群体拥挤并相互堆叠的位置(分别为锥体细胞和神经节细胞的中央凹和中央凹周围),有一个玻璃体到巩膜的层内模式[3H]TdR标记的细胞放置,这反映了发生时间和中央凹期间的运动模式。这些梯度提示了视网膜中细胞命运规范的几种情况,其中许多可能在哺乳动物中不明显,因为哺乳动物发育更快,视网膜结构不太特殊。因此,来自高度特化且发育缓慢的猕猴视网膜的数据可以帮助理解人类的视觉发育,并为未来在其他物种的实验研究指明有用的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatiotemporal gradients of cell genesis in the primate retina.

A cardinal event in the development of all brain structures is the time at which progenitor cells leave the cell cycle and begin to differentiate. We examined cell genesis in the retina of the macaque monkey (Macaca mulatta) by labeling dividing cells with radioactive thymidine ([3H]TdR) and following their fate at terminal division by virtue of their remaining radiolabeled after a long survival period. A number of distinct patterns of cell genesis were observed. The two tissues generated by the optic vesicle, the retinal pigment epithelium and neuroretina, share closely coincident temporal and spatial patterns of cell genesis, indicating that this process may be controlled by a common mechanism. Although overlapping to varying degrees, a clear sequence of genesis was revealed between specific cell types within the neuroretina: ganglion cells are generated first, followed by horizontal cells, cone photoreceptors, amacrine cells, Müller cells, bipolar cells, and, finally, rod photoreceptors. Retinal ganglion cells of differing soma diameter are born at different times-the smallest cells are generated early, the largest late, suggesting a further refined sequence of the functional classes of monkey retinal ganglion cells (first P gamma, then P beta, last P alpha). In addition, at sites where a homogeneous population of cells are crowded and stacked on top of each other (the foveola and perifovea for cones and ganglion cells, respectively) there is a vitreal-to-scleral intralaminar pattern of [3H]TdR labeled cell placement, which reflects both time of genesis and pattern of movement during foveation. These gradients suggest several scenarios for cell fate specification in the retina, many of which might not be obvious in mammals that develop more quickly and have less specialized retinal structure. Thus, data from the highly specialized and slowly developing macaque retina can help to understand visual development in humans and indicate useful avenues for future experimental studies in other species.

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