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Alas1 对斑马鱼中性粒细胞的成熟是必需的。

Alas1 is essential for neutrophil maturation in zebrafish.

机构信息

Key Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases of Guangdong Higher Education Institutes, Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University.

Division of Cell, Developmental and Integrative Biology, School of Medicine, South China University of Technology, Guangzhou, P.R. China.

出版信息

Haematologica. 2018 Nov;103(11):1785-1795. doi: 10.3324/haematol.2018.194316. Epub 2018 Jun 28.

Abstract

Neutrophils play essential roles in innate immunity and are the first responders to kill foreign micro-organisms, a function that partially depends on their granule content. The complicated regulatory network of neutrophil development and maturation remains largely unknown. Here we utilized neutrophil-deficient zebrafish to identify a novel role of Alas1, a heme biosynthesis pathway enzyme, in neutrophil development. We showed that Alas1-deficient zebrafish exhibited proper neutrophil initiation, but further neutrophil maturation was blocked due to heme deficiency, with lipid storage and granule formation deficiencies, and loss of heme-dependent granule protein activities. Consequently, Alas1-deficient zebrafish showed impaired bactericidal ability and augmented inflammatory responses when challenged with These findings demonstrate the important role of Alas1 in regulating neutrophil maturation and physiological function through the heme. Our study provides an model of Alas1 deficiency and may be useful to evaluate the progression of heme-related disorders in order to facilitate the development of drugs and treatment strategies for these diseases.

摘要

中性粒细胞在先天免疫中发挥着重要作用,是杀死外来微生物的第一反应者,这一功能部分依赖于其颗粒内容物。中性粒细胞发育和成熟的复杂调控网络在很大程度上仍不清楚。在这里,我们利用中性粒细胞缺陷斑马鱼来鉴定血红素生物合成途径酶 Alas1 在中性粒细胞发育中的新作用。我们发现 Alas1 缺陷斑马鱼表现出适当的中性粒细胞起始,但由于血红素缺乏,进一步的中性粒细胞成熟被阻断,伴有脂质储存和颗粒形成缺陷,以及丧失血红素依赖性颗粒蛋白活性。因此,当受到细菌感染时, Alas1 缺陷斑马鱼的杀菌能力受损,炎症反应增强。这些发现表明 Alas1 通过血红素在调节中性粒细胞成熟和生理功能方面发挥着重要作用。我们的研究为 Alas1 缺陷提供了一个模型,可能有助于评估血红素相关疾病的进展,从而为这些疾病的药物和治疗策略的发展提供便利。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa61/6278962/f2fe05f4c964/1031785.fig1.jpg

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