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通过质谱成像技术评估珊瑚枝中共生微藻的分子定位。

Assessing Molecular Localization of Symbiont Microalgae in Coral Branches Through Mass Spectrometry Imaging.

机构信息

Department of Marine Science and Resources, College of Bioresource Sciences, Nihon University, 1866 Kameino, , Fujisawa, Kanagawa, 252-0880, Japan.

Department of Biosciences, Faculty of Science and Engineering, Teikyo University, 1-1 Toyosatodai, Utsunomiya-Shi, Tochigi, 320-8551, Japan.

出版信息

Mar Biotechnol (NY). 2024 Apr;26(2):223-229. doi: 10.1007/s10126-024-10294-z. Epub 2024 Feb 12.

Abstract

Reef-building corals are a fundamental pillar of coral reef ecosystems in tropical and subtropical shallow environments. Corals harbor symbiotic dinoflagellates belonging to the family Symbiodiniaceae, commonly known as zooxanthellae. Extensive research has been conducted on this symbiotic relationship, yet the fundamental information about the distribution and localization of Symbiodiniaceae cells in corals is still limited. This information is crucial to understanding the mechanism underlying the metabolite exchange between corals and their algal symbionts, as well as the metabolic flow within holobionts. To examine the distribution of Symbiodiniaceae cells within corals, in this study, we used fluorescence imaging and matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MS-Imaging) on branches of the Acropora tenuis coral. We successfully prepared frozen sections of the coral for molecular imaging without fixing or decalcifying the coral branches. By combining the results of MS-Imaging with that of the fluorescence imaging, we determined that the algal Symbiodiniaceae symbionts were not only localized in the tentacle and surface region of the coral branches but also inhabited the in inner parts. Therefore, the molecular imaging technique used in this study could be valuable to further investigate the molecular dynamics between corals and their symbionts.

摘要

造礁石珊瑚是热带和亚热带浅海环境中珊瑚礁生态系统的重要支柱。珊瑚体内共生着属于虫黄藻科的共生鞭毛藻,通常被称为虫黄藻。目前已经对这种共生关系进行了广泛的研究,但珊瑚体内共生鞭毛藻细胞的分布和定位的基本信息仍然有限。这些信息对于理解珊瑚与其藻类共生体之间代谢物交换的机制以及整个共生体的代谢流至关重要。为了研究珊瑚体内共生鞭毛藻细胞的分布,本研究采用荧光成像和基质辅助激光解吸/电离(MALDI)质谱成像(MS-Imaging)技术对软珊瑚的分支进行了研究。我们成功地在不固定或脱钙珊瑚分支的情况下制备了珊瑚的冷冻切片,用于分子成像。通过将 MS-Imaging 的结果与荧光成像的结果相结合,我们确定藻类共生鞭毛藻不仅定位于珊瑚分支的触须和表面区域,还栖息在内部。因此,本研究中使用的分子成像技术可能有助于进一步研究珊瑚与其共生体之间的分子动态。

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