Primary cell cultures isolated from Penaeus monodon prawns.

L West, T Mahony, F McCarthy, J Watanabe, D Hewitt, S Hansford
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引用次数: 14

Abstract

We have devised a cell culture system for Penaeus monodon prawn cells that uses a defined synthetic medium. Organs were removed from adult prawns ranging in size from 13--19cm rostrum-to-telson length. Cultures consisted of either a blend of hematopoietic and lymphoid cells or ovarian cells. The cells divide rapidly in culture, doubling on average once per week for 5 to 6 weeks. These cultures continue to survive for at least 5 months but the rates of cell division are low after the first 5--6 weeks. In the literature, unicellular eukaryotic marine organisms such as chytrids may contaminate marine cell cultures. In some cases these eukaryotic contaminants may be difficult to distinguish from prawn cells unless detailed ultrastructure or characteristic developmental stages such as zoospores can be observed. Alternatively, we prepared molecular probes from repeated DNA sequences 100--400 bp in length in the P. monodon genome. These species-specific probes were hybridised to genomic DNA from cell culture to confirm proliferation of P. monodon cells in our cultures.

单节对虾原代细胞培养物的分离。
我们设计了一种使用特定合成培养基的单对虾细胞培养系统。从成年对虾的体长从13- 19厘米不等的器官被切除。培养包括造血细胞和淋巴细胞或卵巢细胞的混合。细胞在培养中分裂迅速,平均每周翻倍一次,持续5至6周。这些培养物持续存活至少5个月,但在最初的5- 6周后细胞分裂率很低。在文献中,单细胞真核海洋生物如壶菌可能污染海洋细胞培养物。在某些情况下,这些真核污染物可能很难从对虾细胞中区分出来,除非能观察到详细的超微结构或典型的发育阶段,如游动孢子。另外,我们从单齿疟原虫基因组中长度为100- 400 bp的重复DNA序列中制备分子探针。我们将这些物种特异性探针与细胞培养的基因组DNA杂交,以证实单胞疟原虫细胞在我们的培养中增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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