TY - JOUR
T1 - Isolation, Fixation and Characterization of Juvenile Gilthead Seabream Head Kidney Leukocytes by Flow Cytometry
AU - Marmelo, Isa
AU - Silva, Zélia
AU - Bolotas, Daniel
AU - Alves, Ricardo N.
AU - Videira, Paula A.
AU - Marques, António
AU - Diniz, Mário Sousa
AU - Maulvault, Ana Luísa
N1 - info:eu-repo/grantAgreement/FCT/Concurso de Projetos IC&DT em Todos os Domínios Científicos/PTDC%2FCTA-AMB%2F0592%2F2021/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04378%2F2020/PT#
info:eu-repo/grantAgreement/FCT/Concurso de avaliação no âmbito do Programa Plurianual de Financiamento de Unidades de I&D (2017%2F2018) - Financiamento Base/UIDB%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0140%2F2020/PT#
info:eu-repo/grantAgreement/FCT/3599-PPCDT/2022.04607.PTDC/PT#
info:eu-repo/grantAgreement/FCT/OE/2020.04413.BD/PT#
doi.org/10.54499/PTDC/CTA-AMB/0592/2021#
https://doi.org/10.54499/2020.04413.BD#
Funding Information:
This work was supported by Fundação Portuguesa para a Ciência e Tecnologia (FCT I.P.), under the framework of the project Aqua-CLIMADAPT (PTDC/CTA-AMB/0592/2021, https://doi.org/10.54499/PTDC/CTA-AMB/0592/2021). We acknowledge the BioLab supported by the Applied Molecular Biosciences Unit (UCIBIO) and the Associated Laboratory for Green Chemistry Research Unit-LAQV, which are financed by national funds from FCT/MCTES (UIDB/04378/2020 and UIDB/50006/2020, respectively), as well as the Associate Laboratory Institute for Health and Bioeconomy-i4HB (LA/P/0140/2020). This work was also supported by the European Commission through the GLYCOT winning project (Grant Agreement No. 101079417) and FCT through InnoGlyco (2022.04607.PTDC). Isa Marmelo also acknowledges FCT I.P. for the PhD grant (2020.04413.BD, https://doi.org/10.54499/2020.04413.BD).
Publisher Copyright:
© 2025 JoVE Journal of Visualized Experiments.
PY - 2025/5/9
Y1 - 2025/5/9
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105010355357
U2 - 10.3791/67978
DO - 10.3791/67978
M3 - Article
AN - SCOPUS:105010355357
SN - 1940-087X
VL - 2025-May
JO - Journal of Visualized Experiments
JF - Journal of Visualized Experiments
IS - 219
M1 - e67978
ER -