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从尖吻鲈的脊髓中建立原代细胞培养及鉴定。

Development and characterization of primary cell culture from the spinal cord of Asian seabass, Lates calcarifer.

机构信息

Aquatic Animal Health Laboratory, PG & Research Department of Zoology, C. Abdul Hakeem College (Affiliated Thiruvalluvar University), Melvisharam, 632509, Tamil Nadu, India.

Department of Biochemistry, Saveetha Medical College and Hospital, Saveetha Institute of Medical and Technical Sciences (SIMATS), Thandalam, Chennai, 602105, India.

出版信息

In Vitro Cell Dev Biol Anim. 2024 Sep;60(8):825-831. doi: 10.1007/s11626-024-00938-8. Epub 2024 Aug 5.

Abstract

Asian seabass, Lates calcarifer, is one of the most important fish species in aquaculture. An attempt was made to develop a primary cell culture from the spinal cord of Lates calcarifer by the enzymatic and mechanical dissociation method. The primary cell culture was sub-cultured for 20 times in Leibovitz's L-15 medium with 20% fetal bovine serum (FBS) and 0.5 nM of human neurotrophin-3 at 28°C. The primary cell culture was cryopreserved at different passage levels and recovery of cells after long-term storage was estimated about 75-85%. The authenticity of origin of primary cell culture from L. calcarifer was confirmed by polymerase chain reaction assay using species-specific mitochondrial 12S rRNA primer. The primary cell culture was designated as seabass spinal cord cells (SBSC). The cells morphologically resembled the neurons due to their neural-like prolongations and star-like structure. Immunophenotypic analysis of the SBSC revealed that they are of neuronal origin. The SBSC were found to be highly susceptible to striped jack nervous necrosis virus (SJNNV) and infection in the cells was confirmed by RT-PCR. In conclusion, this is the first innovative euryhaline fish neuronal primary cell culture of L. calcarifer now available for neurophysiological and neurotoxicological studies.

摘要

尖吻鲈,又称亚洲海鲈,是水产养殖中最重要的鱼类之一。本研究尝试通过酶消化和机械分离的方法,从尖吻鲈的脊髓中建立原代细胞培养。原代细胞在含有 20%胎牛血清(FBS)和 0.5nM 人神经营养因子-3 的 Leibovitz's L-15 培养基中于 28°C 下传代 20 次。原代细胞在不同的传代数下进行冻存,长期储存后的细胞回收率约为 75-85%。通过使用种特异性线粒体 12S rRNA 引物的聚合酶链反应分析,证实了原代细胞培养物来自尖吻鲈的真实性。将原代细胞培养物命名为尖吻鲈脊髓细胞(SBSC)。由于其类似神经元的突起和星形结构,细胞形态上类似于神经元。SBSC 的免疫表型分析表明它们起源于神经元。SBSC 对条纹鲈神经坏死病毒(SJNNV)高度敏感,通过 RT-PCR 证实了病毒在细胞中的感染。总之,这是首例尖吻鲈神经原代细胞培养物,适用于神经生理学和神经毒理学研究。

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