Dar Ashaq Sultan, Ahmad Fayaz, Shah Feroz Ahmad, Qadiri Syed Shariq Nazir, Khurshid Keezia
Advanced Research Laboratory, Department of Zoology, University of Kashmir, Hazratbal-190006, Jammu and Kashmir, India.
Division of Aquatic Animal Health and Management (AAHM), Faculty of Fisheries (FoFy), SKUAST Kashmir: Sher-E-Kashmir University of Agricultural Sciences and Technology of Kashmir, Rangil-190006, Jammu and Kashmir, India.
In Vitro Cell Dev Biol Anim. 2025 Feb 5. doi: 10.1007/s11626-025-01018-1.
Here, we successfully grew the SNCF (Schizothorax niger caudal fin) cell line from the caudal fin explants of S. niger, an important cold-water fish of the Himalayas. The cells were successfully grown up to 22 passages by planting explant tissues in DMEM medium supplemented with FBS. We observed optimal cell growth at a concentration of 18% FBS. We observed the steady generation of cells from explants from days 2 to 5 of seeding, and obtained a complete monolayer at days 7-10. We tested various temperatures, including 10 °C, 13 °C, 16 °C, 19 °C, 22 °C, 25 °C, and 28 °C, and found that 22 °C was the optimal temperature for cell growth. We examined the response to various doses of epidermal growth factor (EGF) and fibroblast growth factor (FGF) (0, 2, 4, 6, 8, and 10 ng/mL) on cell colony growth at an optimal temperature of 22 °C. We characterized the cell line using karyotyping at the 14th and 20th passages. The cell line showed epithelial cell-like growth by morphology, which was confirmed by immunotyping. We further used the cell line to study the impact of three pesticides (chlorpyrifos, dimethoate, and endosulfan), and a fungicide (mancozeb) and bacterial extracellular product (ECP). The DAPI stain assay and MTT assay confirmed the pesticides toxic effects on the cells, revealing disintegration of the cell nuclei by the formation of micronuclei and LC concentrations. ECP treatment showed disruption of the monolayer within 0-36 hrs.
在此,我们成功地从喜马拉雅山重要冷水鱼黑裂腹鱼(Schizothorax niger)的尾鳍外植体中培养出了SNCF(黑裂腹鱼尾鳍)细胞系。通过将外植体组织接种于添加了胎牛血清(FBS)的杜氏改良Eagle培养基(DMEM)中,细胞成功传代至22代。我们观察到在FBS浓度为18%时细胞生长最佳。在接种后的第2至5天,我们观察到外植体稳定地产生细胞,并在第7至10天形成完整的单层细胞。我们测试了包括10℃、13℃、16℃、19℃、22℃、25℃和28℃在内的各种温度,发现22℃是细胞生长的最佳温度。在22℃的最佳温度下,我们检测了不同剂量的表皮生长因子(EGF)和成纤维细胞生长因子(FGF)(0、2、4、6、8和10 ng/mL)对细胞集落生长的影响。我们在第14代和第20代时通过核型分析对该细胞系进行了特征鉴定。通过形态学观察,该细胞系呈现上皮样细胞生长,免疫分型进一步证实了这一点。我们进一步使用该细胞系研究了三种农药(毒死蜱、乐果和硫丹)、一种杀菌剂(代森锰锌)和细菌胞外产物(ECP)的影响。4',6-二脒基-2-苯基吲哚(DAPI)染色试验和噻唑蓝(MTT)试验证实了农药对细胞的毒性作用,通过微核形成和半数致死浓度(LC)揭示了细胞核的解体。ECP处理在0至36小时内导致单层细胞破坏。