Rachinsky A, Hartfelder K
USDA Bee Research Laboratory, Beltsville, Maryland 20705, USA.
In Vitro Cell Dev Biol Anim. 1998 Sep;34(8):646-8. doi: 10.1007/s11626-996-0014-x.
We have formulated a tissue culture medium based on the components of larval honey bee hemolymph. Using an in vitro radiochemical assay to measure juvenile hormone biosynthesis, we compared our larval-based medium to four commercially available media (Grace's, Medium-199; Shields and Sang M3, and Minimum Essential Medium), and a medium based on adult honey bee hemolymph. All media were formulated without methionine. There was no significant difference in the amounts of juvenile hormone produced by the larval medium and Grace's; both of these media, however, were more suitable than the remaining four. Our larval-based tissue culture medium should prove useful in studies aimed at elucidating the underlying hormonal mechanism(s) of caste development in honey bees.
我们基于幼虫蜜蜂血淋巴的成分配制了一种组织培养基。使用体外放射化学分析法来测量保幼激素的生物合成,我们将我们的幼虫培养基与四种市售培养基(格雷斯培养基、199培养基、希尔兹和桑格M3培养基以及最低限度基本培养基)以及一种基于成年蜜蜂血淋巴的培养基进行了比较。所有培养基的配方中均不含蛋氨酸。幼虫培养基和格雷斯培养基产生的保幼激素量没有显著差异;然而,这两种培养基都比其余四种更合适。我们基于幼虫的组织培养基在旨在阐明蜜蜂品级发育潜在激素机制的研究中应该会证明是有用的。