GATA factor Serpent promotes phagocytosis in non-professional phagocytes during Drosophila oogenesis.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-03-26 DOI:10.1242/dev.204464
Baosheng Zeng, Haley Grayson, Jianjun Sun
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引用次数: 0

Abstract

Clearance of dying cells is essential for tissue homeostasis and requires both professional and non-professional phagocytes; however, it is unclear what promotes phagocytosis by non-professional phagocytes. Follicle cells of Drosophila egg chambers function as non-professional phagocytes to clear large germ cell debris in mid and late oogenesis, providing an excellent model for the study of non-professional phagocytes. Here we demonstrate that GATA factor Serpent (Srp) plays an indispensable role in promoting the phagocytic capacity of follicle cells in both processes. Srp is upregulated in follicle cells of degenerating mid-stage egg chambers, and its knockdown results in incomplete clearance of germ cell debris and premature follicle cell death. In addition, Srp is upregulated in stretch follicle cells and essential for clearing the nurse cell nuclei in late oogenesis. Genetic analysis reveals that Srp acts downstream of JNK signaling to upregulate the expression of the phagocytic receptor Draper (Drpr) as well as other components in the corpse processing machinery. Our findings highlight the crucial role for Srp in non-professional phagocytes during Drosophila oogenesis, which may also be conserved across species.

GATA因子Serpent在果蝇卵发生过程中促进非专业吞噬细胞的吞噬。
死亡细胞的清除对组织稳态至关重要,需要专业和非专业的吞噬细胞;然而,目前尚不清楚是什么促进了非专业吞噬细胞的吞噬作用。果蝇卵室卵泡细胞作为非专业吞噬细胞,在卵发生中后期清除较大的生殖细胞碎片,为非专业吞噬细胞的研究提供了良好的模型。在这两个过程中,GATA因子Serpent (Srp)在促进卵泡细胞的吞噬能力中起着不可或缺的作用。Srp在变性中期卵室的卵泡细胞中上调,其下调导致生殖细胞碎片的不完全清除和卵泡细胞过早死亡。此外,Srp在拉伸卵泡细胞中表达上调,对于卵子发生后期清除护理细胞核至关重要。遗传分析表明,Srp作用于JNK信号的下游,上调吞噬受体Drpr(吞噬受体Drpr)以及尸体处理机制中其他成分的表达。我们的研究结果强调了Srp在果蝇卵发生过程中对非专业吞噬细胞的关键作用,这也可能在物种间保守。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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