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描述从小鼠胚胎干细胞体外生成Rax阳性视泡的数据。

Data describing Rax positive optic-vesicle generation from mouse embryonic stem cells in vitro.

作者信息

Takata Nozomu, Eiraku Mototsugu, Sakakura Eriko

机构信息

Laboratory for in vitro Histogenesis, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan; Center for Vascular and Developmental Biology, Feinberg Cardiovascular Research Institute, Northwestern University Feinberg School of Medicine, 303 East Superior Street, Chicago 60611, IL, USA.

Laboratory for in vitro Histogenesis, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.

出版信息

Data Brief. 2016 Jun 3;8:465-9. doi: 10.1016/j.dib.2016.05.070. eCollection 2016 Sep.

DOI:10.1016/j.dib.2016.05.070
PMID:27358906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4915947/
Abstract

This article contains data related to the research article entitled "Specification of embryonic stem cell-derived tissues into eye fields by Wnt signaling using rostral diencephalic tissue-inducing culture" Sakakura (2016) [1]. Mouse embryonic stem cells (ESC) were used for the generation of optic vesicle-like tissues in vitro. In this article we described data in which a Rax::GFP knock-in ESC line was used to monitor the formation of optic tissues. In addition, we also described the data of regional marker expression of Rax, Sox2 and Pax6 in vivo around the forebrain and the eye tissues for comparative purposes. These data can be valuable to researchers interested in investigating forebrain and eye tissue development.

摘要

本文包含与研究论文相关的数据,该研究论文题为《利用头侧间脑组织诱导培养通过Wnt信号通路将胚胎干细胞衍生组织定向分化为眼区》,作者坂仓(2016年)[1]。小鼠胚胎干细胞(ESC)被用于体外生成类视泡组织。在本文中,我们描述了使用Rax::GFP基因敲入ESC系来监测视组织形成的数据。此外,为了进行比较,我们还描述了体内前脑和眼组织周围Rax、Sox2和Pax6区域标记物表达的数据。这些数据对于有兴趣研究前脑和眼组织发育的研究人员可能有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b70d/4915947/ab77050a95b0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b70d/4915947/afdbdb2db6f4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b70d/4915947/ab77050a95b0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b70d/4915947/afdbdb2db6f4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b70d/4915947/ab77050a95b0/gr2.jpg

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本文引用的文献

1
Specification of embryonic stem cell-derived tissues into eye fields by Wnt signaling using rostral diencephalic tissue-inducing culture.利用前脑间脑组织诱导培养,通过Wnt信号通路将胚胎干细胞衍生组织定向分化为眼区。
Mech Dev. 2016 Aug;141:90-99. doi: 10.1016/j.mod.2016.05.001. Epub 2016 May 3.
2
Activation of Wnt/ß-catenin signaling in ESC promotes rostral forebrain differentiation in vitro.胚胎干细胞中Wnt/β-连环蛋白信号的激活在体外促进前脑嘴侧分化。
In Vitro Cell Dev Biol Anim. 2016 Mar;52(3):374-382. doi: 10.1007/s11626-015-9975-y. Epub 2015 Nov 12.
3
Mouse embryonic stem cell culture for generation of three-dimensional retinal and cortical tissues.
用于生成三维视网膜和皮质组织的小鼠胚胎干细胞培养。
Nat Protoc. 2011 Dec 15;7(1):69-79. doi: 10.1038/nprot.2011.429.
4
Minimization of exogenous signals in ES cell culture induces rostral hypothalamic differentiation.在胚胎干细胞培养中最小化外源性信号可诱导下丘脑前部分化。
Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11796-801. doi: 10.1073/pnas.0803078105. Epub 2008 Aug 12.
5
Comparative expression of the mouse Sox1, Sox2 and Sox3 genes from pre-gastrulation to early somite stages.从原肠胚形成前期到早期体节阶段小鼠Sox1、Sox2和Sox3基因的表达比较
Mech Dev. 1999 Aug;86(1-2):197-201. doi: 10.1016/s0925-4773(99)00116-1.
6
rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina.Rax是一种新型的配对型同源盒基因,在前神经褶和发育中的视网膜中表达。
Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3088-93. doi: 10.1073/pnas.94.7.3088.
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Developmental appearance, species and tissue specificity of mouse 23-kDa, a retinal calcium-binding protein (recoverin).
Exp Eye Res. 1993 Aug;57(2):189-97. doi: 10.1006/exer.1993.1114.
8
Pax-6, a murine paired box gene, is expressed in the developing CNS.Pax-6是一种小鼠配对盒基因,在发育中的中枢神经系统中表达。
Development. 1991 Dec;113(4):1435-49. doi: 10.1242/dev.113.4.1435.
9
Cloning and sequencing of the 23 kDa mouse photoreceptor cell-specific protein.23千道尔顿小鼠光感受器细胞特异性蛋白的克隆与测序
FEBS Lett. 1992 May 11;302(2):172-6. doi: 10.1016/0014-5793(92)80433-h.