Cell and Tissue Culture Laboratory, Hilleshög AB, Box 302, S-261 23, Landskrona, Sweden.
Plant Cell Rep. 1982 Jun;1(4):151-3. doi: 10.1007/BF00269185.
Datura innoxia cell suspension-derived protoplasts were anchored to Cytodex 1 microcarriers pre-swollen in buffered concanavalin A. As many as 34 protoplasts were estimated to attach per microcarrier, in comparison to a potential 47 as determined from a model based on random anchorage. Fluorescein diacetate was used as localizing agent as well as to assess viability. When included in the swelling medium fluorescence was observed almost instantaneously, first in the protoplast at its interface with the microcarrier, and later throughout the cytoplasm. However, the dye was not conjugated with the lectin, and leakage eventually resulted in fluorescence also of non-anchored protoplasts. Fluorescein-labelled concanavalin A on the other hand permitted detection of microcarriers but not of anchored protoplasts, suggesting the use of differentially fluorescing microcarriers, as an aid in identification of fusion partners.
曼陀罗细胞悬浮培养物原生质体附着在预先在缓冲的伴刀豆球蛋白 A 中膨胀的 Cytodex 1 微载体上。与基于随机附着的模型确定的潜在 47 个相比,每个微载体上估计有多达 34 个原生质体附着。荧光素二乙酸酯既用作定位剂,也用作评估活力的试剂。当包含在膨胀介质中时,荧光几乎立即被观察到,首先在与微载体的界面处的原生质体中,然后在整个细胞质中。然而,该染料未与凝集素缀合,并且泄漏最终导致非附着的原生质体也发出荧光。另一方面,荧光素标记的伴刀豆球蛋白 A 允许检测微载体,但不允许检测附着的原生质体,这表明使用具有不同荧光的微载体作为鉴定融合伙伴的辅助手段。