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Distribution and Characterization of Rhogocyte Cell Types in the Mantle Tissue of Haliotis laevigata

机译:拟南芥(Haliotis laevigata)的地幔组织中的红细胞类型和分布特征。

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Molluscan rhogocytes are known to be the only cells able to synthesize hemocyanin that is one of the largest respiratory proteins in nature. However, investigation of rhogocyte cells in vitro is limited due to difficulty in isolating and establishing marine cell culture. The aim of this study was to investigate the nature and distribution of rhogocyte cells of Haliotis laevigata in the mantle tissue with respect to the expression of the two known isoforms of hemocyanin. Rhogocyte cells were identified using immunofluorescence-fluorescence in situ hybridization (IF-FISH) that involved simultaneous staining of localized hemocyanin by a polyclonal antibody while the mRNA was hybridized with FISH probes. The distribution of rhogocyte cells was demonstrated using flow cytometry, followed by cell sorting with fluorescence-activated cell sorter (FACS) and confocal microscope imaging for further characterization. Our results suggested that the mantle tissue is dominated by two distinct populations of rhogocyte cells that synthesize hemocyanin type 1. Observation with confocal microscopy of both populations revealed hemocyanin localization in the periphery of the cell membrane. Cell population with higher antibody signal had irregular and elongated cell morphology with punctate mRNA probe signals. The second population with lower antibody signal had ovoid morphology and wide distribution of mRNA probe signals. We suggest that these populations represent two distinct phases of hemocyanin biosynthesis of a single isoform, which is closely related to Haliotis tuberculata type 1 hemocyanin (HtH1). The knowledge acquired in this study enhances the understanding of the biology of rhogocyte cells and biosynthesis of hemocyanin.
机译:已知软体动物的流变细胞是唯一能够合成血色素的细胞,而血色素是自然界中最大的呼吸蛋白之一。然而,由于难以分离和建立海洋细胞培养物,体外对白细胞的研究受到限制。这项研究的目的是调查血红蛋白的两种已知同工型的表达情况,研究披风鲍氏藻在套层组织中的特性和分布。使用免疫荧光-荧光原位杂交(IF-FISH)鉴定了流血细胞,该杂交涉及通过多克隆抗体同时染色局部血蓝蛋白,同时将mRNA与FISH探针杂交。流式细胞仪证实了流纹细胞的分布,随后用荧光激活细胞分选仪(FACS)进行了细胞分选和共聚焦显微镜成像以进一步表征。我们的研究结果表明,套细胞组织由合成血红蛋白1型的两个不同的流血细胞群体控制。用共聚焦显微镜观察这两个群体发现血红蛋白位于细胞膜的外围。抗体信号较高的细胞群体具有点状mRNA探针信号的不规则和延长的细胞形态。具有较低抗体信号的第二群体具有卵形形态和mRNA探针信号的广泛分布。我们建议这些人群代表单一同工型的血蓝蛋白生物合成的两个不同阶段,这与结核杆菌Haliotis tuberculata 1型血蓝蛋白(HtH1)密切相关。在这项研究中获得的知识增进了对流血细胞生物学和血蓝蛋白生物合成的理解。

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