Isolation of coelomocyte from sea urchin Echinometra mathaei: optimization of culture condition.

IF 1.7 4区 生物学 Q4 CELL BIOLOGY
Fatemeh Piryaei, Pargol Ghavam Mostafavi, Razieh Dalirfardouei, Fahimeh Piryaei
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Abstract

Rapid growth of the aquaculture industry is hampered by infectious diseases in marine invertebrates, causing economic losses. Marine invertebrate cell cultures offer tools to evaluate biological properties and cellular responses in different conditions. Long-term culture aims to isolate tissue-specific cells and identify bioactive compounds from stem cells. Echinometra mathaei, known as Persian Gulf sea urchin, has lots of benefits in various fields including aquaculture, embryology, and evolutionary biology. However, its cell culture faces challenges due to poorly characterized microenvironmental and specific cultivation requirements. This study aims to establish and optimize a long-term cell culture for coelomocyte derived from E. mathaei, focusing on the characterization of microenvironment conditions to overcome the limitations of current marine invertebrate cell culture. After the collection of E. mathaei from Lark Island, Persian Gulf, Iran, and their acclimatization in artificial seawater, coelomocytes were isolated from different sources including the coelomic fluid, the coelomic epithelium, and the axial organ. Various cell dissociation methods, culture media, growth supplements, culture dishes, and physical conditions were tested to determine optimal conditions for coelomocyte in vitro culture. Moreover, coelomocytes were differentiated to pigment-producing cells, and naphthoquinone pigments were extracted and identified using spectrophotometry. Light microscopy identified several coelomocyte types, including petaloid, filopodial, vibratile cells, and spherulocytes. The HCCM medium supplemented with coelomic fluid proved most effective for cell growth and viability. Moreover, coelomic fluid is the best culture media for differentiation of coelomocyte into the cell producing naphthoquinone pigments. These findings contribute to developing in vitro cell culture methods for sea urchin, providing a foundation for further research on sea urchin immunology, cell biology, and cellular responses to pathogens and other biological stress.

海胆胆腔细胞的分离及培养条件的优化。
水产养殖业的快速增长受到海洋无脊椎动物传染病的阻碍,造成经济损失。海洋无脊椎动物细胞培养为评估不同条件下的生物特性和细胞反应提供了工具。长期培养旨在分离组织特异性细胞并从干细胞中鉴定生物活性化合物。波斯湾海胆(Echinometra mathaei)在水产养殖、胚胎学和进化生物学等各个领域都有很多好处。然而,由于微环境特征不明确和特定的培养要求,其细胞培养面临挑战。本研究旨在建立并优化mataaei腔骨细胞的长期细胞培养,重点研究微环境条件的表征,以克服目前海洋无脊椎动物细胞培养的局限性。在伊朗云雀岛采集毛蚶,经人工海水驯化后,分别从体腔液、体腔上皮和轴向器官中分离出体腔细胞。我们测试了各种细胞分离方法、培养基、生长补充剂、培养皿和物理条件,以确定体外培养腔胚细胞的最佳条件。此外,体腔细胞分化为色素生成细胞,并通过分光光度法提取和鉴定萘醌色素。光镜下发现了几种体腔细胞类型,包括花瓣状细胞、丝状细胞、振动细胞和球型细胞。经证实,添加体腔液的HCCM培养基对细胞生长和活力最有效。体腔液是体腔细胞向萘醌类色素细胞分化的最佳培养基。这些研究结果有助于建立海胆体外细胞培养方法,为进一步研究海胆免疫学、细胞生物学以及细胞对病原体和其他生物胁迫的反应提供基础。
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来源期刊
CiteScore
3.70
自引率
4.80%
发文量
96
审稿时长
3 months
期刊介绍: In Vitro Cellular & Developmental Biology - Animal is a journal of the Society for In Vitro Biology (SIVB). Original manuscripts reporting results of research in cellular, molecular, and developmental biology that employ or are relevant to organs, tissue, tumors, and cells in vitro will be considered for publication. Topics covered include: Biotechnology; Cell and Tissue Models; Cell Growth/Differentiation/Apoptosis; Cellular Pathology/Virology; Cytokines/Growth Factors/Adhesion Factors; Establishment of Cell Lines; Signal Transduction; Stem Cells; Toxicology/Chemical Carcinogenesis; Product Applications.
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