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幼蛙视网膜中神经元生成的细胞特异性调控。

Cell-specific regulation of neuronal production in the larval frog retina.

作者信息

Reh T A

机构信息

Department of Medical Physiology, University of Calgary, Alberta, Canada.

出版信息

J Neurosci. 1987 Oct;7(10):3317-24. doi: 10.1523/JNEUROSCI.07-10-03317.1987.

DOI:10.1523/JNEUROSCI.07-10-03317.1987
PMID:3499488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6569163/
Abstract

We have previously postulated the existence of a feedback mechanism from differentiated neurons that regulates the production of new neurons. Evidence for such regulatory feedback comes from experiments in which dopamine-containing amacrine cells, ablated in the developing retina by 6-hydroxydopamine (6-OHDA), were up-regulated in their production. To determine whether this is a general phenomenon of the developing retina, the neurotoxin kainic acid (KA) was injected intraocularly in midlarval-stage Rana pipiens tadpoles to produce selective lesions of certain retinal cell types. After periods of 1-21 d, the animals received intraperitoneal injections of 3H-thymidine. Animals were then allowed to survive for periods of up to 3 weeks and were then fixed, the eyes embedded in plastic, sectioned at 3 micron, and processed for autoradiography by standard methods. At the dosage used, the KA produced a 52% decline in the cell density of the inner nuclear layer (INL), a 37% decline in the retinal ganglion cell layer (RGC), and no significant change in the density of cells in the outer nuclear layer (ONL). The 3H-thymidine allowed us to detect any changes in the number of new cells added to the retina after the KA lesion. Within the first week after the KA injection, there was a decrease in the number of 3H-thymidine (3H-Thy)-labeled cells in the lesioned eye as compared to in the control retina; however, KA treatment of slice cultures demonstrated that the toxin does not affect proliferating neuroblasts directly.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前曾推测,已分化的神经元存在一种反馈机制,可调节新神经元的产生。这种调节性反馈的证据来自以下实验:在发育中的视网膜中,用6-羟基多巴胺(6-OHDA)消融含多巴胺的无长突细胞后,其产生量上调。为了确定这是否是发育中视网膜的普遍现象,将神经毒素红藻氨酸(KA)眼内注射到中幼体阶段的牛蛙蝌蚪体内,以对某些视网膜细胞类型产生选择性损伤。在1至21天的时间段后,给动物腹腔注射3H-胸腺嘧啶核苷。然后让动物存活长达3周,随后固定,将眼睛包埋在塑料中,切成3微米厚的切片,并通过标准方法进行放射自显影处理。在所使用的剂量下,KA使内核层(INL)的细胞密度下降了52%,视网膜神经节细胞层(RGC)的细胞密度下降了37%,而外核层(ONL)的细胞密度没有显著变化。3H-胸腺嘧啶核苷使我们能够检测KA损伤后视网膜中新添加细胞数量的任何变化。在KA注射后的第一周内,与对照视网膜相比,损伤眼中3H-胸腺嘧啶核苷(3H-Thy)标记的细胞数量减少;然而,KA对切片培养物的处理表明,该毒素不会直接影响增殖的成神经细胞。(摘要截于250字)

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