Cornet M
Laboratoire d'Océanographie biologique, Université de Bordeaux-I, Talence.
C R Acad Sci III. 1992;315(1):7-12.
Explants from mantle and foot tissues of adult mussel were grown in culture tubes containing a medium composed of Eagle's Basal Medium supplemented with salts, Hepes buffer, egg yolk and antibiotics. The cultures were maintained at 18 degrees C and pH 7.50, without medium renewal. After 6-7 days, the cultures were stopped and harvested for slide preparation. Numerous metaphase spreads that were good enough for karyotyping were consistently obtained. This method may prove to be a reliable source of actively dividing cells that is a prerequisite for extensive chromosome structure analyses in the bivalves.
将成年贻贝外套膜和足部组织的外植体接种于装有由伊格尔基础培养基添加盐类、羟乙基哌嗪乙磺酸缓冲液、蛋黄和抗生素组成的培养基的培养管中。培养物维持在18℃、pH 7.50的条件下,不更换培养基。6 - 7天后,停止培养并收获用于制备玻片。始终能获得大量足以进行核型分析的中期染色体铺展。该方法可能被证明是一个可靠的活跃分裂细胞来源,而活跃分裂细胞是双壳贝类广泛染色体结构分析的一个先决条件。