Joshi Bhupali, Chatterji Anil, Bhonde Ramesh
National Centre for Cell Science, NCCS Complex, Ganaeshkhind, Pune 411007, India.
In Vitro Cell Dev Biol Anim. 2002 May;38(5):255-7. doi: 10.1290/1071-2690(2002)038<0255:LTIVGO>2.0.CO;2.
Amoebocyte is the single type of cell circulating in the horseshoe crab hemolymph, which plays a major role in the defense system of the animal. Granules present in these cells are sensitive to nanogram quantities of bacterial endotoxins, which form the basis of the Limulus amoebocyte lysate (LAL) test. Normally, amoebocytes for the production of the LAL are collected by cardiac puncture; hence, development of the in vitro culture system for amoebocytes will reduce the variability of the lysate and help to conserve the 400 million-yr-old living fossil. In the present investigation we have attempted organ culture of gill flaps that have been shown to be the source of amoebocytes. The gill flaps were cultured at 28 degrees C on a rocker platform in a modified L-15 medium supplemented with 10% v/v horseshoe crab serum. This led to the release of amoebocytes outside the gill flaps for a period of 6-8 wk with a more or less steady number of amoebocytes during the weekly harvest. No significant difference was seen in the yield of amoebocytes from male and female horseshoe crabs. Confocal laser microscopy studies revealed significant difference in the size of amoebocytes released in vitro as compared with those obtained in vivo. Thus, we have optimized the culture conditions for the long-term generation of amoebocytes in vitro from the Indian horseshoe crab Tachypleus gigas by reducing the incidence of contamination, simulating in vivo conditions for the organ culture of gill flaps, and improvising the nutritional status using the modified L-15 medium, providing the desired osmolarity and pH.
变形细胞是鲎血淋巴中循环的唯一细胞类型,在该动物的防御系统中起主要作用。这些细胞中的颗粒对纳克量的细菌内毒素敏感,这构成了鲎试剂(LAL)检测的基础。通常,用于生产LAL的变形细胞是通过心脏穿刺收集的;因此,变形细胞体外培养系统的开发将减少裂解物的变异性,并有助于保护这种有着4亿年历史的活化石。在本研究中,我们尝试对已被证明是变形细胞来源的鳃瓣进行器官培养。将鳃瓣在28摄氏度下于摇床上在添加了10%(体积/体积)鲎血清的改良L-15培养基中培养。这导致鳃瓣外释放变形细胞长达6至8周,每周收获时变形细胞数量或多或少保持稳定。雌雄鲎产生的变形细胞产量没有显著差异。共聚焦激光显微镜研究显示,与体内获得的变形细胞相比,体外释放的变形细胞大小存在显著差异。因此,我们通过降低污染发生率、模拟鳃瓣器官培养的体内条件以及使用改良L-15培养基改善营养状况,提供所需的渗透压和pH值,优化了从印度鲎巨鲎体外长期生成变形细胞的培养条件。