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本文引用的文献

1
mpeg1 promoter transgenes direct macrophage-lineage expression in zebrafish.mpeg1 启动子转基因在斑马鱼中指导巨噬细胞谱系表达。
Blood. 2011 Jan 27;117(4):e49-56. doi: 10.1182/blood-2010-10-314120. Epub 2010 Nov 17.
2
Clonal analyses reveal roles of organ founding stem cells, melanocyte stem cells and melanoblasts in establishment, growth and regeneration of the adult zebrafish fin.克隆分析揭示了成体斑马鱼鳍的建立、生长和再生过程中器官起始干细胞、黑素细胞干细胞和黑素前体细胞的作用。
Development. 2010 Dec;137(23):3931-9. doi: 10.1242/dev.057075. Epub 2010 Oct 27.
3
MAZe: a tool for mosaic analysis of gene function in zebrafish.MAZe:一种用于斑马鱼基因功能马赛克分析的工具。
Nat Methods. 2010 Mar;7(3):219-23. doi: 10.1038/nmeth.1423. Epub 2010 Feb 7.
4
Molecular signaling networks that choreograph epimorphic fin regeneration in zebrafish - a mini-review.分子信号网络在斑马鱼肢体再生中的时空调控作用——一篇小综述。
Gerontology. 2010;56(2):231-40. doi: 10.1159/000259327. Epub 2009 Nov 18.
5
Limb blastema cell: a stem cell for morphological regeneration.肢体芽基细胞:形态再生的干细胞。
Dev Growth Differ. 2010 Jan;52(1):89-99. doi: 10.1111/j.1440-169X.2009.01144.x. Epub 2009 Nov 5.
6
Normal table of postembryonic zebrafish development: staging by externally visible anatomy of the living fish.正常斑马鱼胚胎发育表:根据活体鱼的外部可见解剖结构进行分期。
Dev Dyn. 2009 Dec;238(12):2975-3015. doi: 10.1002/dvdy.22113.
7
Cells keep a memory of their tissue origin during axolotl limb regeneration.在蝾螈肢体再生过程中,细胞保留着它们组织起源的记忆。
Nature. 2009 Jul 2;460(7251):60-5. doi: 10.1038/nature08152.
8
Collagen IX is required for the integrity of collagen II fibrils and the regulation of vascular plexus formation in zebrafish caudal fins.IX型胶原蛋白对于斑马鱼尾鳍中II型胶原蛋白纤维的完整性以及血管丛形成的调节是必需的。
Dev Biol. 2009 Aug 15;332(2):360-70. doi: 10.1016/j.ydbio.2009.06.003. Epub 2009 Jun 6.
9
Development of diverse lateral line patterns on the teleost caudal fin.硬骨鱼尾鳍上多样侧线模式的发育。
Dev Dyn. 2008 Oct;237(10):2889-902. doi: 10.1002/dvdy.21710.
10
Gene expression analysis on sections of zebrafish regenerating fins reveals limitations in the whole-mount in situ hybridization method.对斑马鱼再生鳍切片进行的基因表达分析揭示了整体原位杂交方法的局限性。
Dev Dyn. 2008 Feb;237(2):417-25. doi: 10.1002/dvdy.21417.

斑马鱼鳍的生长和再生中的命运限制。

Fate restriction in the growing and regenerating zebrafish fin.

机构信息

Department of Genetics, Washington University Medical School, St Louis, MO 63110, USA.

出版信息

Dev Cell. 2011 May 17;20(5):725-32. doi: 10.1016/j.devcel.2011.04.013.

DOI:10.1016/j.devcel.2011.04.013
PMID:21571228
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3096007/
Abstract

We use transposon-based clonal analysis to identify the lineage classes that make the adult zebrafish caudal fin. We identify nine distinct lineage classes, including epidermis, melanocyte/xanthophore, iridophore, intraray glia, lateral line, osteoblast, dermal fibroblast, vascular endothelium, and resident blood. These lineage classes argue for distinct progenitors, or organ founding stem cells (FSCs), for each lineage, which retain fate restriction throughout growth of the fin. Thus, distinct FSCs exist for the four neuroectoderm lineages, and dermal fibroblasts are not progenitors for fin ray osteoblasts; however, artery and vein cells derive from a shared lineage in the fin. Transdifferentiation of cells or lineages in the regeneration blastema is often postulated. However, our studies of single progenitors or FSCs reveal no transfating or transdifferentiation between these lineages in the regenerating fin. This result shows that, the same as in growth, lineages retain fate restriction when passed through the regeneration blastema.

摘要

我们使用转座子克隆分析来鉴定构成成年斑马鱼尾鳍的谱系类群。我们确定了九个不同的谱系类群,包括表皮、黑素细胞/黄色素细胞、虹彩细胞、间 ray 神经胶质细胞、侧线、成骨细胞、真皮成纤维细胞、血管内皮细胞和固有血细胞。这些谱系类群表明每个谱系都有独特的祖细胞或器官起始干细胞(FSCs),它们在 fin 的生长过程中保持命运限制。因此,四个神经外胚层谱系存在不同的 FSCs,而真皮成纤维细胞不是 fin 射线成骨细胞的祖细胞;然而,动脉和静脉细胞来源于 fin 中的共享谱系。细胞或谱系在再生芽基中的转分化经常被假设。然而,我们对单个祖细胞或 FSCs 的研究表明,在再生的 fin 中,这些谱系之间没有转分化或转分化。这个结果表明,与生长一样,谱系在通过再生芽基时保持命运限制。