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建立腔肠动物 Nematostella vectensis 和 Pocillopora damicornis 全身原代细胞培养的新方法。

Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis.

机构信息

Rosenstiel School of Marine and Atmospheric Science, University of Miami, 4600 Rickenbacker Causeway, Miami, FL, 33149, USA.

Biology Department, University of Maryland, 4094 Campus Drive, College Park, MD, 20742, USA.

出版信息

Sci Rep. 2021 Feb 18;11(1):4086. doi: 10.1038/s41598-021-83549-7.

Abstract

Cnidarians are emerging model organisms for cell and molecular biology research. However, successful cell culture development has been challenging due to incomplete tissue dissociation and contamination. In this report, we developed and tested several different methodologies to culture primary cells from all tissues of two species of Cnidaria: Nematostella vectensis and Pocillopora damicornis. In over 170 replicated cell cultures, we demonstrate that physical dissociation was the most successful method for viable and diverse N. vectensis cells while antibiotic-assisted dissociation was most successful for viable and diverse P. damicornis cells. We also demonstrate that a rigorous antibiotic pretreatment results in less initial contamination in cell cultures. Primary cultures of both species averaged 12-13 days of viability, showed proliferation, and maintained high cell diversity including cnidocytes, nematosomes, putative gastrodermal, and epidermal cells. Overall, this work will contribute a needed tool for furthering functional cell biology experiments in Cnidaria.

摘要

刺胞动物是细胞和分子生物学研究的新兴模式生物。然而,由于组织解离不完全和污染,成功的细胞培养发展一直具有挑战性。在本报告中,我们开发并测试了几种不同的方法来培养两种刺胞动物(Nemastostella vectensis 和 Pocillopora damicornis)所有组织的原代细胞。在超过 170 个重复的细胞培养中,我们证明物理解离是获得活力和多样性的 N. vectensis 细胞的最成功方法,而抗生素辅助解离是获得活力和多样性的 P. damicornis 细胞的最成功方法。我们还证明,严格的抗生素预处理可减少细胞培养物中的初始污染。两种物种的原代培养物的平均存活时间为 12-13 天,显示出增殖,并保持高细胞多样性,包括刺细胞、神经体、假定的胃皮和表皮细胞。总的来说,这项工作将为刺胞动物的功能细胞生物学实验提供一个急需的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed6/7893170/355f9da69380/41598_2021_83549_Fig1_HTML.jpg

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