Suppr超能文献

微藻细胞周期动力学:光照时间和药物的影响。

Cell Cycle Dynamics in the Microalga : Influence of Light Duration and Drugs.

机构信息

Laboratoire GenAlg Nantes, Unité Physiologie et Toxines des Microalgues Toxine (PHYTOX), IFREMER F-44311 Nantes, France.

Laboratoire PhysAlg Nantes, Unité Physiologie et Toxines des Microalgues Toxine (PHYTOX), IFREMER F-44311 Nantes, France.

出版信息

Cells. 2024 Nov 20;13(22):1925. doi: 10.3390/cells13221925.

Abstract

Our investigation into 's cell cycle regulation involved natural and chemical synchronization methods to maximize their proportion at the division phase (G). Hence, cultures were grown under different light/dark cycles (24:0, 12:12, and 8:16 h) to assess the impact of extended dark periods on cell division. Flow cytometry analyses of the cell cycle revealed that extending the dark phase resulted in a higher number of cells entering G. However, this remained a minority within the overall culture (peaking at 19.36% ± 0.17 under an 8:16 h L/D cycle). To further enhance synchronization, chemical agents (nocodazole, hydroxyurea, and aphidicolin) were tested for their efficacy in blocking specific cell cycle stages. Only aphidicolin successfully induced significant G accumulation (>90%). The commitment point for cell division was examined by exposing cultures to varying light durations (0 to 8 h) and measuring cell concentration and size distribution every 4 h. Our findings identified a critical minimum cell size ("sizer") of approximately 56.2 ± 0.6 µm and a required minimal light exposure ("timer") of 4 h to reliably trigger cell division. These findings highlight key conditions needed for optimal division of , offering more controlled and efficient cultivation strategies for future biotechnological applications.

摘要

我们对's 的细胞周期调控的研究涉及自然和化学同步化方法,以最大限度地提高其在分裂期(G 期)的比例。因此,我们在不同的光照/黑暗周期(24:0、12:12 和 8:16 h)下培养细胞,以评估延长黑暗期对细胞分裂的影响。细胞周期的流式细胞术分析表明,延长黑暗期会导致更多的细胞进入 G 期。然而,在整个培养物中,这仍然是少数(在 8:16 h L/D 周期下达到峰值,为 19.36%±0.17)。为了进一步增强同步性,我们测试了化学试剂(诺考达唑、羟基脲和阿非迪霉素)在阻断特定细胞周期阶段的效果。只有阿非迪霉素成功地诱导了显著的 G 期积累(>90%)。我们通过暴露培养物于不同的光照持续时间(0 至 8 h)并每隔 4 h测量细胞浓度和大小分布来检查细胞分裂的决定点。我们的研究结果确定了一个关键的最小细胞大小(“定标器”)约为 56.2±0.6 µm,以及一个最小的光照暴露(“定时器”)4 h,以可靠地触发细胞分裂。这些发现突出了细胞最佳分裂所需的关键条件,为未来生物技术应用提供了更具控制性和高效性的培养策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d298/11592524/c0b09c97ad64/cells-13-01925-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验