Uehara Ren, Takeda Shinji, Oku Daichi, Sasaki Ryo, Murakami Masaru, Shiba Hajime, Katakura Fumihiko, Moritomo Tadaaki
Department of Veterinary Medicine, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, 252-0880, Japan.
Laboratory of Molecular Biology, Azabu University School of Veterinary Medicine, Sagamihara, Kanagawa, 252-5201, Japan.
Dev Comp Immunol. 2025 Jan;162:105290. doi: 10.1016/j.dci.2024.105290. Epub 2024 Nov 19.
The clonal triploid ginbuna crucian carp Carassius auratus langsdorfii, a naturally occurring gynogenetic fish, is suitable for cell transplantation studies to reveal the roles of stem cells and immune cells. To ensure long-term traceability of donor cells within recipient fish, we have established a transgenic ginbuna line that expresses green fluorescent protein (GFP). The Xenopus laevis ef1a promoter was introduced for regulating GFP expression. Tol2 transposon-based transgenesis to ginbuna embryos resulted in producing a putative founder fish (F0) in a mosaic fluorescent fashion; the frequency of germline transmission was 14.9%. All embryos of GFP-positive offspring (F1)-derived F2 generation expressed GFP widely across the body. The result of Southern blot analysis showed that the transgene was present on a single DNA fragment of equivalent size among F1 and F2 individuals tested, indicating that the transgene was stably transmitted without translocation. Analysis of the fluorescence intensity of organs obtained from F1 and F2 juveniles using fluorescence microscope showed that eyes, brain, skeletal muscle, heart and gonad exhibited a strong GFP fluorescence while gill, spleen and intestine gave a weak signal; no fluorescence was observed in erythrocytes. Flow cytometric analyses of peripheral leukocytes from F1 and F2 adult fish revealed all cell populations expressed GFP. Scale grafts from the transgenic fish to the wild-type fish exhibited persistent engraftment. Together, our transgenic line can be a powerful tool for studying cellular dynamics by cell transplantation and provide a solid basis for further immunological research advances in teleost.
克隆三倍体银鲫(Carassius auratus langsdorfii)是一种自然发生的雌核发育鱼类,适合用于细胞移植研究以揭示干细胞和免疫细胞的作用。为了确保供体细胞在受体鱼体内的长期可追踪性,我们建立了一个表达绿色荧光蛋白(GFP)的转基因银鲫品系。引入非洲爪蟾(Xenopus laevis)的ef1a启动子来调控GFP的表达。基于Tol2转座子的转基因技术应用于银鲫胚胎,产生了一条以镶嵌荧光方式存在的假定奠基鱼(F0);种系传递频率为14.9%。GFP阳性后代(F1)的F2代所有胚胎在全身广泛表达GFP。Southern印迹分析结果表明,在所测试的F1和F2个体中,转基因存在于大小相当的单个DNA片段上,这表明转基因能够稳定传递且无易位现象。使用荧光显微镜对F1和F2幼鱼的器官荧光强度进行分析,结果显示眼睛、大脑、骨骼肌、心脏和性腺呈现强烈的GFP荧光,而鳃、脾脏和肠道发出微弱信号;红细胞中未观察到荧光。对F1和F2成年鱼外周白细胞进行流式细胞术分析,结果显示所有细胞群体均表达GFP。将转基因鱼的鳞片移植到野生型鱼上,移植效果持久。总之,我们的转基因品系可以成为通过细胞移植研究细胞动态的有力工具,并为硬骨鱼进一步的免疫学研究进展提供坚实基础。