...
首页> 外文期刊>In Vitro Cellular & Developmental Biology - Animal >Separation and viability of gill and hepatopancreatic cells of a mangrove crab Ucides cordatus
【24h】

Separation and viability of gill and hepatopancreatic cells of a mangrove crab Ucides cordatus

机译:红树林蟹U和肝胰腺of细胞和肝胰腺细胞的分离和生存力

获取原文
获取原文并翻译 | 示例

摘要

The gills contain essential cells for respiration and osmoregulation, whereas the hepatopancreas is the site of digestion, absorption, and nutrients storage. The aim of this work was to separate and characterize gill and hepatopancreatic cells of the mangrove crab, Ucides cordatus. For gills, the methodology consisted of an enzymatic cellular dissociation using Trypsin at 0.5%, observation of cellular viability with Tripan Blue, and separation of cells using discontinuous sucrose gradient at concentrations of 10%, 20%, 30%, and 40%. The hepatopancreatic cells were dissociated by magnetic stirring, with posterior separation by sucrose gradient at the same concentrations above. For gills, a high cellular viability was observed (92.5±2.1%), with hemocyte cells in 10% sucrose layer (57.99 ± 0.17%, *P < 0.05), principal cells in the 20% sucrose layer (57.33 ± 0.18, *P < 0.05), and thick cells and pillar cells in the 30% and 40% sucrose layers, respectively (39.54 ± 0.05%, *P < 0.05; and 41.81 ± 0.04%, *P < 0.05). The hepatopancreatic cells also showed good viability (79.22 ± 0.02%), with the observation of embryonic (E) cells in the 10% sucrose layer (67.87 ± 0.06%, **P < 0.001), resorptive (R) and fibrillar (F) cells in the 20% and 30% sucrose layers (44.71 ± 0.06%, **P < 0.001, and 43.25 ± 0.01%, *P < 0.05; respectively), and blister (B) cells in the 40% sucrose layer (63.09 ± 0.03%, **P < 0.001). The results are a starting point for in vitro studies of heavy metal transport in isolated cells of the mangrove crab U. cordatus, subjected to contamination by metals in the mangrove habitat where they are found.
机译:contain含有呼吸和渗透调节所需的细胞,而肝胰脏则是消化,吸收和养分储存的场所。这项工作的目的是分离和表征美洲红树蟹(Ucides cordatus)的g和肝胰腺细胞。对于g,该方法包括使用胰蛋白酶0.5%进行酶促细胞解离,使用Tripan Blue观察细胞活力以及使用浓度为10%,20%,30%和40%的不连续蔗糖梯度分离细胞。通过磁力搅拌使肝胰脏细胞解离,并通过蔗糖梯度以相同的浓度在后方分离。对于g,观察到较高的细胞生存力(92.5±2.1%),其中10%蔗糖层中的血细胞为(57.99±0.17%,* P <0.05),20%蔗糖层中的主细胞为(57.33±0.18,*) P <0.05),以及分别在30%和40%蔗糖层中的厚细胞和柱状细胞(39.54±0.05%,* P <0.05;和41.81±0.04%,* P <0.05)。肝胰腺细胞也显示出良好的活力(79.22±0.02%),在10%蔗糖层中观察到了胚胎(E)细胞(67.87±0.06%,** P <0.001),吸收性(R)和原纤维(F )20%和30%蔗糖层中的细胞(分别为44.71±0.06%,** P <0.001和43.25±0.01%,* P <0.05;)和40%蔗糖层中的起泡(B)细胞( 63.09±0.03%,** P <0.001)。该结果是体外研究红树林蟹脐带分离细胞中重金属迁移的起点,该重金属在发现它们的红树林生境中受到金属的污染。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号