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本文引用的文献

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Vertebrate neural cell-fate determination: lessons from the retina.脊椎动物神经细胞命运的决定:来自视网膜的启示
Nat Rev Neurosci. 2001 Feb;2(2):109-18. doi: 10.1038/35053522.
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Müller cell differentiation in the zebrafish neural retina: evidence of distinct early and late stages in cell maturation.斑马鱼神经视网膜中的米勒细胞分化:细胞成熟过程中不同早期和晚期阶段的证据。
J Comp Neurol. 2001 Jan 22;429(4):530-40. doi: 10.1002/1096-9861(20010122)429:4<530::aid-cne2>3.0.co;2-c.
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Harnessing the power of forward genetics--analysis of neuronal diversity and patterning in the zebrafish retina.利用正向遗传学的力量——斑马鱼视网膜中神经元多样性和模式形成的分析
Trends Neurosci. 2000 Nov;23(11):531-41. doi: 10.1016/s0166-2236(00)01655-6.
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Genetic analysis of eye development in zebrafish.斑马鱼眼睛发育的遗传分析。
Results Probl Cell Differ. 2000;31:257-82. doi: 10.1007/978-3-540-46826-4_13.
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Rhodopsin trafficking and its role in retinal dystrophies.视紫红质的运输及其在视网膜营养不良中的作用。
Int Rev Cytol. 2000;195:215-67. doi: 10.1016/s0074-7696(08)62706-0.
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Retinal degeneration in tulp1-/- mice: vesicular accumulation in the interphotoreceptor matrix.tulp1基因敲除小鼠的视网膜变性:光感受器间基质中的囊泡积聚。
Invest Ophthalmol Vis Sci. 1999 Nov;40(12):2795-802.
7
Genetic disorders of vision revealed by a behavioral screen of 400 essential loci in zebrafish.通过对斑马鱼400个必需基因座的行为筛选揭示的视觉遗传疾病。
J Neurosci. 1999 Oct 1;19(19):8603-15. doi: 10.1523/JNEUROSCI.19-19-08603.1999.
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Retinoic acid promotes rod photoreceptor differentiation in rat retina in vivo.维甲酸在体内促进大鼠视网膜视杆光感受器细胞分化。
Neuroreport. 1999 Aug 2;10(11):2389-94. doi: 10.1097/00001756-199908020-00031.
9
Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice.从abcr基因敲除小鼠的表型深入了解视网膜蛋白在光感受器中的功能及斯塔加特病的病因。
Cell. 1999 Jul 9;98(1):13-23. doi: 10.1016/S0092-8674(00)80602-9.
10
Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3.缺乏环核苷酸门控通道CNG3的小鼠中视锥细胞功能的选择性丧失。
Proc Natl Acad Sci U S A. 1999 Jun 22;96(13):7553-7. doi: 10.1073/pnas.96.13.7553.

早期光感受器发育的一种突变——mikre oko,揭示了斑马鱼光感受器存活和分化过程中涉及的细胞间相互作用。

A mutation of early photoreceptor development, mikre oko, reveals cell-cell interactions involved in the survival and differentiation of zebrafish photoreceptors.

作者信息

Doerre G, Malicki J

机构信息

Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts 02114, USA.

出版信息

J Neurosci. 2001 Sep 1;21(17):6745-57. doi: 10.1523/JNEUROSCI.21-17-06745.2001.

DOI:10.1523/JNEUROSCI.21-17-06745.2001
PMID:11517263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6763086/
Abstract

To gain insight into mechanisms involved in photoreceptor development, we characterized a zebrafish mutation in the mikre oko locus that produces early loss of photoreceptor cells. mikre oko photoreceptors lose their elongated morphology at the time of wild-type outer segment formation and undergo cell death within a few days. To investigate whether this phenotype involves cell-cell interaction defects, we performed analysis of genetically mosaic animals. Interactions of mikre oko photoreceptors with wild-type cells rescue several aspects of the mutant phenotype. When placed in a wild-type environment, mikre oko photoreceptor cells retain elongated morphology and survive longer. Moreover, although mutant mikre oko photoreceptor outer segments develop only infrequently and are usually disorganized, mikre oko cone and rod cells in mosaic retinas develop robust outer segments that closely resemble the wild type. In contrast to the outer segments, the proximal regions of mikre oko photoreceptor cells, including their inner segments, the nuclear regions, and the synaptic termini, retain the mutant appearance. mikre oko outer segment rescue is not mediated by interactions with the retinal pigment epithelium. These studies demonstrate that the differentiation of outer segments is surprisingly independent from the more proximal photoreceptor cell features and that outer segment development includes retinal pigment epithelium-independent cell-cell interactions.

摘要

为深入了解光感受器发育所涉及的机制,我们对mikre oko基因座中的斑马鱼突变进行了表征,该突变导致光感受器细胞早期缺失。在野生型外段形成时,mikre oko光感受器失去其细长形态,并在几天内发生细胞死亡。为研究这种表型是否涉及细胞间相互作用缺陷,我们对基因嵌合体动物进行了分析。mikre oko光感受器与野生型细胞的相互作用挽救了突变体表型的几个方面。当置于野生型环境中时,mikre oko光感受器细胞保持细长形态并存活更长时间。此外,虽然突变的mikre oko光感受器外段很少发育且通常杂乱无章,但嵌合视网膜中的mikre oko视锥细胞和视杆细胞发育出与野生型非常相似的强健外段。与外段不同,mikre oko光感受器细胞的近端区域,包括其内段、核区域和突触末端,保持突变外观。mikre oko外段的挽救不是由与视网膜色素上皮的相互作用介导的。这些研究表明,外段的分化出人意料地独立于更近端的光感受器细胞特征,并且外段发育包括不依赖于视网膜色素上皮的细胞间相互作用。