Costa María M, Paredes Estefania, Peleteiro Mercedes, Sánchez-Ruiloba Lucía, Gambón Francisco, Dios Sonia, Gestal Camino
Instituto de Investigaciones Marinas (IIM), CSIC, Vigo, Spain.
Coastal Ecology Research Group (ECOCOST), Department of Ecology and Animal Biology, Marine Research Center, University of Vigo, Vigo, Spain.
Front Immunol. 2025 Mar 21;16:1543587. doi: 10.3389/fimmu.2025.1543587. eCollection 2025.
The common octopus, Cuvier 1797, as all cephalopods, presents highly evolved characteristics compared to other classes of molluscs and the whole invertebrate phyla. However, to date, there is not much information about its immune system, and studying the defense mechanisms is a key step in understanding their response to external aggressions, having the tools to anticipate animal health problems and ensure their welfare. The lack of cell cultures in molluscs is a major problem when carrying out assays that help to deepen our knowledge of this species' main immune cells. Cryopreservation becomes an alternative to maintaining viable and functional cells after freezing/thawing processes. Having access to good high-quality cells for long periods allows cover a wider repertoire of studies, time courses, and the avoidance of logistical issues such as loss of viability and/or functionality, time constraints, or sample transport challenges. Additionally, high-quality cell suspensions are essential for successful applications, such as single-cell sequencing, where viability and functionality are the key to optimal identification. The optimal medium, cryoprotective agent, and freezing/thawing protocol for octopus hemocytes have been selected. We show here the first functional results from cryopreserved hemocytes. Cells cryopreserved in MAS medium supplemented with EG maintained viability above 80% after 15 weeks post cryopreservation storage at -80°C, and their functional ability to phagocytize bacteria similar to fresh cells. Moreover, thawed acclimated cells exhibited a gene expression pattern comparable to fresh cells, as opposed to directly thawed cells. The acclimation process after thawing was essential to recover the functional activity of the cells and to return to levels of gene expression involved in oxidative stress similar to fresh cells.The results presented here will facilitate functional studies of octopus immune cells and provide tools for cell preservation in other molluscs species.
普通章鱼(居维叶,1797年)与所有头足类动物一样,与其他类别的软体动物和整个无脊椎动物门相比,具有高度进化的特征。然而,迄今为止,关于其免疫系统的信息并不多,研究防御机制是了解它们对外界侵害反应的关键一步,拥有相关工具对于预测动物健康问题并确保其福利至关重要。在进行有助于深入了解该物种主要免疫细胞的试验时,软体动物缺乏细胞培养是一个主要问题。冷冻保存成为在冷冻/解冻过程后维持细胞存活和功能的一种替代方法。长时间获得优质的细胞能够涵盖更广泛的研究范围、时间进程,并避免诸如活力和/或功能丧失、时间限制或样品运输挑战等后勤问题。此外,高质量的细胞悬液对于成功应用至关重要,例如单细胞测序,其中活力和功能是最佳鉴定的关键。已经选择了章鱼血细胞的最佳培养基、冷冻保护剂和冷冻/解冻方案。我们在此展示了冷冻保存血细胞的首批功能结果。在添加了乙二醇(EG)的MAS培养基中冷冻保存的细胞,在-80°C冷冻保存15周后,活力保持在80%以上,并且它们吞噬细菌的功能能力与新鲜细胞相似。此外,解冻后适应的细胞表现出与新鲜细胞相当的基因表达模式,这与直接解冻的细胞不同。解冻后的适应过程对于恢复细胞的功能活性以及使参与氧化应激的基因表达水平恢复到与新鲜细胞相似的水平至关重要。本文呈现的结果将有助于章鱼免疫细胞的功能研究,并为其他软体动物物种的细胞保存提供工具。