Isolation, Fixation and Characterization of Juvenile Gilthead Seabream Head Kidney Leukocytes by Flow Cytometry.

IF 1.2 4区 综合性期刊 Q3 MULTIDISCIPLINARY SCIENCES
Isa Marmelo, Zélia Silva, Daniel Bolotas, Ricardo N Alves, Paula A Videira, António Marques, Mário Sousa Diniz, Ana Luísa Maulvault
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Abstract

Immunity is crucial for the physiological regulation of organisms, serving as the primary defense against pathogens and environmental stressors. The isolation and analysis of immune cells provide key insights into immune responses to external pressures. However, the lack of harmonized protocols for less studied species, such as marine fish, often leads to technical and analytical challenges that hamper data interpretation and a thorough understanding of species-specific immune responses. This study aimed to set up an optimized flow cytometry-based analytical procedure to characterize and determine the viability of leukocytes from the head kidney (the main hematopoietic organ in teleost fish) of juvenile gilthead seabream (Sparus aurata). The procedure began with the isolation of leukocytes through a homogenization process using Hanks' balanced salt solution, followed by an optimized Percoll density gradient centrifugation method to ensure high recovery rates of leukocytes with minimal erythrocyte contamination required for efficient subsequent flow cytometry analysis. Additionally, a novel technique using a cell-reactive dye (LIVE/DEAD Fixable Dead Cell Stain Kit) was employed to distinguish viable from dead cells based on their fluorescent staining patterns. Fixation was achieved with 3.7% formaldehyde, preserving cell morphology, viability, and staining efficiency. Flow cytometry analysis successfully identified three predominant leukocyte populations: lymphocytes, monocytes, and granulocytes. This method not only allowed viability tests but also the accurate differentiation of cell types. The improvement in flow cytometry protocols represents a step forward in fish immunology by increasing the accuracy and efficiency of immune cell analysis. Furthermore, by allowing the fixation of cells for later analysis, this protocol significantly reduces the time and effort required for immune assessments, making it a valuable tool for both research and practical applications in various fields of research.

幼鱼头肾白细胞的分离、固定及流式细胞术鉴定。
免疫对生物体的生理调节至关重要,是抵御病原体和环境应激源的主要防御手段。免疫细胞的分离和分析提供了对外部压力的免疫反应的关键见解。然而,对海洋鱼类等研究较少的物种缺乏统一的议定书,往往导致技术和分析方面的挑战,妨碍了数据解释和对物种特异性免疫反应的彻底了解。本研究旨在建立一种优化的基于流式细胞术的分析方法,以表征和测定幼鱼头肾(硬骨鱼的主要造血器官)白细胞的活力。首先,使用Hanks平衡盐溶液通过均质过程分离白细胞,然后采用优化的Percoll密度梯度离心方法,以确保白细胞的高回收率和最小的红细胞污染,从而进行高效的后续流式细胞术分析。此外,一种使用细胞活性染料的新技术(LIVE/DEAD Fixable DEAD Cell Stain Kit)被用于根据荧光染色模式区分活细胞和死细胞。3.7%的甲醛固定,保持细胞形态、活力和染色效率。流式细胞术分析成功地鉴定了三种主要的白细胞群:淋巴细胞、单核细胞和粒细胞。这种方法不仅可以进行活力测试,而且可以准确地区分细胞类型。流式细胞术方案的改进通过提高免疫细胞分析的准确性和效率,代表了鱼类免疫学向前迈进了一步。此外,通过允许细胞固定以供以后分析,该方案大大减少了免疫评估所需的时间和精力,使其成为研究和实际应用于各个研究领域的宝贵工具。
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来源期刊
Jove-Journal of Visualized Experiments
Jove-Journal of Visualized Experiments MULTIDISCIPLINARY SCIENCES-
CiteScore
2.10
自引率
0.00%
发文量
992
期刊介绍: JoVE, the Journal of Visualized Experiments, is the world''s first peer reviewed scientific video journal. Established in 2006, JoVE is devoted to publishing scientific research in a visual format to help researchers overcome two of the biggest challenges facing the scientific research community today; poor reproducibility and the time and labor intensive nature of learning new experimental techniques.
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