School of Medicine, Deakin University, Geelong, Victoria, Australia.
Institute of Mental and Physical Health and Clinical Translation (IMPACT), Deakin University, Geelong, Victoria, Australia.
J Innate Immun. 2024;16(1):262-282. doi: 10.1159/000538364. Epub 2024 Apr 24.
Signal transducer and activator of transcription (STAT) 3 is extensively involved in the development, homeostasis, and function of immune cells, with STAT3 disruption associated with human immune-related disorders. The roles ascribed to STAT3 have been assumed to be due to its canonical mode of action as an inducible transcription factor downstream of multiple cytokines, although alternative noncanonical functional modalities have also been identified. The relative involvement of each mode was further explored in relevant zebrafish models.
Genome editing with CRISPR/Cas9 was used to generate mutants of the conserved zebrafish Stat3 protein: a loss of function knockout (KO) mutant and a mutant lacking C-terminal sequences including the transactivation domain (ΔTAD). Lines harboring these mutations were analyzed with respect to blood and immune cell development and function in comparison to wild-type zebrafish.
The Stat3 KO mutant showed perturbation of hematopoietic lineages throughout primitive and early definitive hematopoiesis. Neutrophil numbers did not increase in response to lipopolysaccharide (LPS) or granulocyte colony-stimulating factor (G-CSF) and their migration was significantly diminished, the latter correlating with abrogation of the Cxcl8b/Cxcr2 pathway, with macrophage responses perturbed. Intriguingly, many of these phenotypes were not shared by the Stat3 ΔTAD mutant. Indeed, only neutrophil and macrophage development were disrupted in these mutants with responsiveness to LPS and G-CSF maintained, and neutrophil migration actually increased.
This study has identified roles for zebrafish Stat3 within hematopoietic stem cells impacting multiple lineages throughout primitive and early definitive hematopoiesis, myeloid cell responses to G-CSF and LPS and neutrophil migration. Many of these roles showed conservation, but notably several involved noncanonical modalities, providing additional insights for relevant diseases.
信号转导子和转录激活子(STAT)3 广泛参与免疫细胞的发育、稳态和功能,STAT3 破坏与人类免疫相关疾病有关。STAT3 的作用归因于其作为多种细胞因子下游诱导转录因子的经典作用模式,尽管也已经确定了替代的非经典功能模式。在相关的斑马鱼模型中进一步探讨了每种模式的相对参与度。
使用 CRISPR/Cas9 进行基因组编辑,生成保守的斑马鱼 Stat3 蛋白的突变体:功能丧失敲除(KO)突变体和缺失包括转录激活域(ΔTAD)在内的 C 端序列的突变体。与野生型斑马鱼相比,分析这些突变体的血液和免疫细胞发育以及功能。
Stat3 KO 突变体在原始和早期确定性造血过程中造血谱系受到干扰。脂多糖(LPS)或粒细胞集落刺激因子(G-CSF)刺激后中性粒细胞数量没有增加,其迁移明显减少,后者与 Cxcl8b/Cxcr2 途径的阻断有关,巨噬细胞反应受到干扰。有趣的是,这些表型中的许多并不为 Stat3 ΔTAD 突变体所共有。事实上,只有中性粒细胞和巨噬细胞发育在这些突变体中受到干扰,对 LPS 和 G-CSF 的反应保持不变,并且中性粒细胞迁移实际上增加。
本研究确定了斑马鱼 Stat3 在造血干细胞中的作用,影响原始和早期确定性造血过程中的多个谱系,髓样细胞对 G-CSF 和 LPS 的反应以及中性粒细胞迁移。其中许多作用具有保守性,但值得注意的是,一些作用涉及非经典模式,为相关疾病提供了更多的见解。