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本文引用的文献

1
A short receptor downregulates JAK/STAT signalling to control the Drosophila cellular immune response.短受体下调 JAK/STAT 信号通路以控制果蝇细胞免疫反应。
PLoS Biol. 2010 Aug 3;8(8):e1000441. doi: 10.1371/journal.pbio.1000441.
2
chinmo is a functional effector of the JAK/STAT pathway that regulates eye development, tumor formation, and stem cell self-renewal in Drosophila.Chinmo 是 JAK/STAT 通路的一个功能性效应因子,它在果蝇中调节眼睛发育、肿瘤形成和干细胞自我更新。
Dev Cell. 2010 Apr 20;18(4):556-68. doi: 10.1016/j.devcel.2010.02.006.
3
Hematopoietic stem cells in Drosophila.果蝇中的造血干细胞。
Development. 2010 Jan;137(1):27-31. doi: 10.1242/dev.043943.
4
Upregulation of the Drosophila Friend of GATA gene U-shaped by JAK/STAT signaling maintains lymph gland prohemocyte potency.果蝇中GATA基因U型的朋友基因通过JAK/STAT信号上调维持淋巴腺前血细胞的潜能。
Mol Cell Biol. 2009 Nov;29(22):6086-96. doi: 10.1128/MCB.00244-09. Epub 2009 Sep 8.
5
Genome-wide expression profiling in the Drosophila eye reveals unexpected repression of notch signaling by the JAK/STAT pathway.果蝇眼睛中的全基因组表达谱揭示了JAK/STAT通路对Notch信号的意外抑制。
Dev Dyn. 2009 Sep;238(9):2235-53. doi: 10.1002/dvdy.21989.
6
Partial loss of GATA factor Pannier impairs adult heart function in Drosophila.GATA因子Pannier的部分缺失会损害果蝇的成年心脏功能。
Hum Mol Genet. 2009 Sep 1;18(17):3153-63. doi: 10.1093/hmg/ddp254. Epub 2009 Jun 3.
7
Dual role of wingless signaling in stem-like hematopoietic precursor maintenance in Drosophila.无翅信号在果蝇造血前体细胞维持中的双重作用。
Dev Cell. 2009 May;16(5):756-63. doi: 10.1016/j.devcel.2009.03.003.
8
Sessile hemocytes as a hematopoietic compartment in Drosophila melanogaster.无柄血细胞作为黑腹果蝇的一个造血区室。
Proc Natl Acad Sci U S A. 2009 Mar 24;106(12):4805-9. doi: 10.1073/pnas.0801766106. Epub 2009 Mar 4.
9
Definition of Drosophila hemocyte subsets by cell-type specific antigens.通过细胞类型特异性抗原定义果蝇血细胞亚群。
Acta Biol Hung. 2007;58 Suppl:95-111. doi: 10.1556/ABiol.58.2007.Suppl.8.
10
pannier encodes two structurally related isoforms that are differentially expressed during Drosophila development and display distinct functions during thorax patterning.背篓基因编码两种结构相关的亚型,它们在果蝇发育过程中差异表达,并在胸部模式形成过程中发挥不同功能。
Mech Dev. 2008 Jan-Feb;125(1-2):43-57. doi: 10.1016/j.mod.2007.10.008. Epub 2007 Oct 24.

JAK/STAT 和 GATA 因子 Pannier 控制果蝇血细胞的成熟和分化。

JAK/STAT and the GATA factor Pannier control hemocyte maturation and differentiation in Drosophila.

机构信息

Waksman Institute, Rutgers University, 190 Frelinghuysen Rd Piscataway, NJ 08854, USA.

出版信息

Dev Biol. 2011 Apr 15;352(2):308-16. doi: 10.1016/j.ydbio.2011.01.035. Epub 2011 Feb 3.

DOI:10.1016/j.ydbio.2011.01.035
PMID:21295568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065540/
Abstract

The lymph gland is the major site of hematopoiesis in Drosophila. During late larval stages three types of hemocytes are produced, plasmatocytes, crystal cells, and lamellocytes, and their differentiation is tightly controlled by conserved factors and signaling pathways. JAK/STAT is one of these pathways which have essential roles in vertebrate and fly hematopoiesis. We show that Stat has opposing cell-autonomous and non-autonomous functions in hemocyte differentiation. Using a clonal approach we established that loss of Stat in a set of prohemocytes in the cortical zone induces plasmatocyte maturation in adjacent hemocytes. Hemocytes lacking Stat fail to differentiate into plasmatocytes, indicating that Stat positively and cell-autonomously controls plasmatocyte differentiation. We also identified the GATA factor pannier (pnr) as a downstream target of Stat. By analyzing the phenotypes resulting from clonal loss and over-expression of pnr in lymph glands, we find that Pnr is positively regulated by Stat and specifically required for the differentiation of plasmatocytes. Stat and Pnr represent two essential factors controlling blood cell maturation in the developing lymph gland and exert their functions both in a cell-autonomous and non-cell-autonomous manner.

摘要

淋巴腺是果蝇造血的主要部位。在幼虫后期,会产生三种血细胞,浆细胞、晶体细胞和膜细胞,它们的分化受到保守因子和信号通路的严格控制。JAK/STAT 就是这些通路之一,它在脊椎动物和果蝇的造血中具有重要作用。我们发现 Stat 在血细胞分化中具有自主和非自主的相反作用。我们通过克隆方法确定,在皮质区的一组前血细胞中缺失 Stat 会诱导相邻血细胞中的浆细胞成熟。缺乏 Stat 的血细胞无法分化为浆细胞,这表明 Stat 正向自主地控制浆细胞分化。我们还确定了 GATA 因子 pannier(pnr)是 Stat 的下游靶标。通过分析淋巴腺中 pnr 克隆缺失和过表达的表型,我们发现 Pnr 受 Stat 正向调控,并且是浆细胞分化所必需的。Stat 和 Pnr 是控制发育中淋巴腺血细胞成熟的两个必需因素,它们以自主和非自主的方式发挥作用。