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IL7-hCD25 and IL7-Cre BAC transgenic mouse lines: new tools for analysis of IL-7 expressing cells.IL7-hCD25和IL7-Cre BAC转基因小鼠品系:用于分析表达IL-7细胞的新工具。
Genesis. 2009 Apr;47(4):281-7. doi: 10.1002/dvg.20497.
2
Increased thymus- and decreased parathyroid-fated organ domains in Splotch mutant embryos.斑纹突变胚胎中胸腺注定器官域增加而甲状旁腺注定器官域减少。
Dev Biol. 2009 Mar 1;327(1):216-27. doi: 10.1016/j.ydbio.2008.12.019. Epub 2008 Dec 25.
3
Alterations in the thymocyte phenotype of EphB-deficient mice largely affect the double negative cell compartment.EphB基因缺陷小鼠胸腺细胞表型的改变主要影响双阴性细胞区室。
Immunology. 2008 Sep;125(1):131-43. doi: 10.1111/j.1365-2567.2008.02828.x. Epub 2008 Apr 4.
4
Neural crest origin of perivascular mesenchyme in the adult thymus.成年胸腺中血管周围间充质的神经嵴起源
J Immunol. 2008 Apr 15;180(8):5344-51. doi: 10.4049/jimmunol.180.8.5344.
5
Contribution of neural crest-derived cells in the embryonic and adult thymus.神经嵴衍生细胞在胚胎期和成年期胸腺中的作用。
J Immunol. 2008 Mar 1;180(5):3183-9. doi: 10.4049/jimmunol.180.5.3183.
6
EphrinB1-EphB signaling regulates thymocyte-epithelium interactions involved in functional T cell development.EphrinB1-EphB信号传导调节参与功能性T细胞发育的胸腺细胞与上皮细胞间的相互作用。
Eur J Immunol. 2007 Sep;37(9):2596-605. doi: 10.1002/eji.200737097.
7
Specific expression of lacZ and cre recombinase in fetal thymic epithelial cells by multiplex gene targeting at the Foxn1 locus.通过在Foxn1基因座进行多重基因靶向,使lacZ和cre重组酶在胎儿胸腺上皮细胞中特异性表达。
BMC Dev Biol. 2007 Jun 18;7:69. doi: 10.1186/1471-213X-7-69.
8
EphrinA1 activates a Src/focal adhesion kinase-mediated motility response leading to rho-dependent actino/myosin contractility.埃弗林A1激活一种由Src/粘着斑激酶介导的运动反应,导致依赖于rho的肌动蛋白/肌球蛋白收缩。
J Biol Chem. 2007 Jul 6;282(27):19619-28. doi: 10.1074/jbc.M701319200. Epub 2007 Apr 22.
9
Ephrin-B2 forward signaling regulates somite patterning and neural crest cell development.埃菲林-B2正向信号传导调节体节模式形成和神经嵴细胞发育。
Dev Biol. 2007 Apr 1;304(1):182-93. doi: 10.1016/j.ydbio.2006.12.028. Epub 2006 Dec 19.
10
Defective ALK5 signaling in the neural crest leads to increased postmigratory neural crest cell apoptosis and severe outflow tract defects.神经嵴中ALK5信号缺陷会导致迁移后神经嵴细胞凋亡增加以及严重的流出道缺陷。
BMC Dev Biol. 2006 Nov 1;6:51. doi: 10.1186/1471-213X-6-51.

EphB-ephrin-B2 相互作用是器官发生过程中胸腺迁移所必需的。

EphB-ephrin-B2 interactions are required for thymus migration during organogenesis.

机构信息

Molecular Immunology, National Institute of Medical Research, London NW7 1AA, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13414-9. doi: 10.1073/pnas.1003747107. Epub 2010 Jul 8.

DOI:10.1073/pnas.1003747107
PMID:20616004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2922182/
Abstract

Thymus organogenesis requires coordinated interactions of multiple cell types, including neural crest (NC) cells, to orchestrate the formation, separation, and subsequent migration of the developing thymus from the third pharyngeal pouch to the thoracic cavity. The molecular mechanisms driving these processes are unclear; however, NC-derived mesenchyme has been shown to play an important role. Here, we show that, in the absence of ephrin-B2 expression on thymic NC-derived mesenchyme, the thymus remains in the cervical area instead of migrating into the thoracic cavity. Analysis of individual NC-derived thymic mesenchymal cells shows that, in the absence of ephrin-B2, their motility is impaired as a result of defective EphB receptor signaling. This implies a NC-derived cell-specific role of EphB-ephrin-B2 interactions in the collective migration of the thymic rudiment during organogenesis.

摘要

胸腺器官发生需要多种细胞类型的协调相互作用,包括神经嵴 (NC) 细胞,以协调发育中的胸腺从第三咽囊到胸腔的形成、分离和随后的迁移。驱动这些过程的分子机制尚不清楚;然而,已经表明 NC 衍生的间充质在其中发挥了重要作用。在这里,我们表明,在胸腺 NC 衍生的间充质上缺乏 Ephrin-B2 表达的情况下,胸腺仍然位于颈部区域,而不是迁移到胸腔中。对单个 NC 衍生的胸腺间充质细胞的分析表明,在缺乏 Ephrin-B2 的情况下,由于 EphB 受体信号的缺陷,它们的迁移能力受损。这意味着 EphB-ephrin-B2 相互作用在器官发生过程中胸腺原基的集体迁移中具有 NC 衍生的细胞特异性作用。