Structural diversity and function of the granulocyte colony-stimulating factor in medaka fish.

IF 2.5 4区 医学 Q2 HEMATOLOGY
Ayame Ogawa, Shungo Konno, Satoshi Ansai, Kiyoshi Naruse, Takashi Kato
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引用次数: 0

Abstract

Diversity in the granulocyte repertoire, including neutrophils, basophils, and eosinophils, has been reported in vertebrate species. Medaka fish (Oryzias latipes) have only neutrophils; however, the storage pool of granulopoiesis tissues and the molecular mechanism of granulopoiesis in medaka fish have not been explored. Granulocyte colony-stimulating factor (G-CSF) is a cytokine responsible for neutrophil differentiation, survival, and proliferation. We performed in silico analysis to molecularly characterize the medaka G-CSF and G-CSF receptor (G-CSFR) genes. This study showed that medaka G-CSF differs considerably from human and mouse G-CSF in terms of the primary protein structure; however, the predicted tertiary structure was largely conserved. Analyses of lipopolysaccharide stimulation and G-CSF knockout and overexpression in medaka revealed that G-CSF mobilizes neutrophils into the peripheral blood. The analysis of G-CSF-deficient medaka revealed that G-CSF is involved in erythropoiesis. These findings represent an important first step toward understanding granulocyte hematopoiesis in non-mammalian species.

青鳉体内粒细胞集落刺激因子的结构多样性与功能
据报道,脊椎动物中的粒细胞具有多样性,包括中性粒细胞、嗜碱性粒细胞和嗜酸性粒细胞。青鳉鱼(Oryzias latipes)只有中性粒细胞;然而,青鳉鱼中粒细胞生成组织的储存库和粒细胞生成的分子机制尚未得到探索。粒细胞集落刺激因子(G-CSF)是一种细胞因子,负责中性粒细胞的分化、存活和增殖。我们对青鳉的 G-CSF 和 G-CSF 受体(G-CSFR)基因进行了分子分析。研究结果表明,青鳉 G-CSF 与人类和小鼠 G-CSF 的一级蛋白结构有很大不同,但预测的三级结构基本保持一致。对脂多糖刺激和青鳉体内 G-CSF 基因敲除和过表达的分析表明,G-CSF 能动员中性粒细胞进入外周血。对 G-CSF 缺陷青鳉的分析表明,G-CSF 参与红细胞生成。这些发现为了解非哺乳动物的粒细胞造血迈出了重要的第一步。
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来源期刊
Experimental hematology
Experimental hematology 医学-血液学
CiteScore
5.30
自引率
0.00%
发文量
84
审稿时长
58 days
期刊介绍: Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.
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