Rel governs loser elimination during stem cell competition in the Drosophila testis

IF 4.5 3区 生物学 Q2 CELL BIOLOGY
Silvana Hof-Michel , Ljubinka Cigoja , Sabina Huhn , Christian Bökel
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引用次数: 0

Abstract

In the Drosophila testis, a group of stromal cells termed hub provides multiple niche signals for the surrounding germline and somatic stem cells. Stem cells of both populations compete for physical retention in the niche, and clones unable to transduce any one niche signal are rapidly eliminated from the stem cell pool by differentiation. We have mapped the transcriptomes of isolated somatic cyst stem cells and differentiated cyst cells, and found that the stem cells but not their differentiated progeny exhibit the signature of an innate immune response including the NF-κB transcription factor Relish (Rel). Related signalling pathways had previously implicated in cell competition in larval epithelia, prompting the question of whether NF-κB signalling was, despite the clear differences between the two competition scenarios, also involved in stem cell competition in the testis. Here we show i) that in the testis Rel is dispensable for stemness, ii) that loss of Rel or the upstream receptor Toll suppresses loser elimination following a variety of different triggers used to induce loser fate, and iii) that clonal Rel activation is sufficient for the displacement of neutral or winner cells from the niche, even if these cells otherwise retain stem cell properties.

Rel控制果蝇睾丸中干细胞竞争过程中的失败者淘汰。
在果蝇的睾丸中,一组被称为hub的基质细胞为周围的种系和体细胞干细胞提供多种生态位信号。两种群体的干细胞为了在生态位中的物理保留而竞争,不能转导任何一个生态位信号的克隆通过分化迅速从干细胞库中消除。我们绘制了分离的体细胞囊肿干细胞和分化的囊肿细胞的转录组图,发现干细胞而不是其分化的后代表现出包括NF-κB转录因子(Rel)在内的先天免疫反应的特征。相关信号通路先前涉及幼虫上皮细胞竞争,这引发了一个问题,即尽管两种竞争情况存在明显差异,NF-κB信号是否也参与睾丸干细胞竞争。在这里,我们证明了1)在睾丸中,Rel对于干细胞是不可缺少的,ii) Rel或上游受体Toll的缺失抑制了在各种不同的触发因素诱导失败者命运后的失败者消除,iii)克隆Rel激活足以使中性细胞或赢家细胞从生态位中位移,即使这些细胞保留了干细胞特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European journal of cell biology
European journal of cell biology 生物-细胞生物学
CiteScore
7.30
自引率
1.50%
发文量
80
审稿时长
38 days
期刊介绍: The European Journal of Cell Biology, a journal of experimental cell investigation, publishes reviews, original articles and short communications on the structure, function and macromolecular organization of cells and cell components. Contributions focusing on cellular dynamics, motility and differentiation, particularly if related to cellular biochemistry, molecular biology, immunology, neurobiology, and developmental biology are encouraged. Manuscripts describing significant technical advances are also welcome. In addition, papers dealing with biomedical issues of general interest to cell biologists will be published. Contributions addressing cell biological problems in prokaryotes and plants are also welcome.
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