Department of zoology, Goa University, Taleigao plateau, Goa, 403206, India.
Cytotechnology. 2008 Mar;56(3):161-9. doi: 10.1007/s10616-008-9152-1. Epub 2008 Jun 7.
This paper reports for the first time, the Primary cell culture of hepatopancreas from edible crab Scylla serrata using crab saline, L-15 (Leibovitz), 1 x L-15 + crab saline, 2 x L-15 + crab saline, 3 x L-15 and citrate buffer without any serum. We could isolate and maintain E (Embryonalzellen), F (Fibrenzellen), B (Blasenzellen), R (Restzellen) and G (Granular cells). Upon seeding the hepatopancreatic E, F, B, and R cells showed different survival pattern over time than granular cells. A modified L-15 (3x) medium supported the best survival of hepatopancreatic E, F B, and R cells in in-vitro culture. However granular cells could be maintained for 184 days with L-15 (1x) + crab saline. Fetal bovine serum was not effective additive and hampered cell viability in present study.
本文首次报道了使用蟹盐水、L-15(Leibovitz)、1 x L-15 + 蟹盐水、2 x L-15 + 蟹盐水、3 x L-15 和柠檬酸盐缓冲液,在无任何血清的情况下从食用蟹锯缘青蟹(Scylla serrata)的肝胰腺中进行原代细胞培养。我们可以分离并维持 E(胚胎细胞)、F(纤维细胞)、B(囊泡细胞)、R(休止细胞)和 G(颗粒细胞)。在接种肝胰腺 E、F、B 和 R 细胞后,它们的存活模式随时间呈现出与颗粒细胞不同的特点。改良的 L-15(3x)培养基在体外培养中最有利于肝胰腺 E、F、B 和 R 细胞的存活。然而,颗粒细胞可以在 L-15(1x)+蟹盐水的条件下维持 184 天。在本研究中,胎牛血清不是有效的添加剂,反而会损害细胞活力。