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首页> 外文期刊>BMC Developmental Biology >Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
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Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration

机译:长期延时实时成像显示,在脊髓灰质炎再生期间大量细胞迁移

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Background Time-lapse imaging has proven highly valuable for studying development, yielding data of much finer resolution than traditional “still-shot” studies and allowing direct examination of tissue and cell dynamics. A major challenge for time-lapse imaging?of animals is keeping specimens immobile yet healthy for extended periods of time. Although this is often feasible for embryos, the difficulty of immobilizing typically motile juvenile and adult stages remains a persistent obstacle to time-lapse imaging of post-embryonic development. Results Here we describe a new method for long-duration time-lapse imaging of adults of the small freshwater annelid Pristina leidyi and use this method to investigate its regenerative processes. Specimens are immobilized with tetrodotoxin, resulting in irreversible paralysis yet apparently normal regeneration, and mounted in agarose surrounded by culture water or halocarbon oil, to prevent dehydration but allowing gas exchange. Using this method, worms can be imaged continuously and at high spatial-temporal resolution for up to 5?days, spanning the entire regeneration process. We performed a fine-scale analysis of regeneration growth rate and characterized cell migration dynamics during early regeneration. Our studies reveal the migration of several putative cell types, including one strongly resembling published descriptions of annelid neoblasts, a cell type suggested to be migratory based on “still-shot” studies and long hypothesized to be linked to regenerative success in annelids. Conclusions Combining neurotoxin-based paralysis, live mounting techniques and a starvation-tolerant study system has allowed us to obtain the most extensive high-resolution longitudinal recordings of full anterior and posterior regeneration in an invertebrate, and to detect and characterize several cell types undergoing extensive migration during this process. We expect the tetrodotoxin paralysis and time-lapse imaging methods presented here to be broadly useful in studying other animals and of particular value for studying post-embryonic development.
机译:背景技术延时成像已被证明对研究发育非常有价值,其产生的数据分辨率比传统的“静态”研究好得多,并且可以直接检查组织和细胞动力学。对动物进行延时成像的一个主要挑战是要保持标本不动,但要长期保持健康。尽管这对于胚胎通常是可行的,但是固定通常活动的少年和成年阶段的困难仍然是胚胎发育后延时成像的持续障碍。结果在这里,我们描述了一种新的方法,用于小型淡水无核小虾Pristina leidyi的成年成年人的长时间延时成像,并使用该方法研究其再生过程。标本固定在河豚毒素中,导致不可逆的瘫痪,但显然可正常再生,并安装在琼脂糖中,并用培养水或卤化碳油包围,以防止脱水但允许气体交换。使用这种方法,可以在整个再生过程中连续5天内以高时空分辨率连续成像蠕虫。我们进行了再生生长速率的精细分析,并表征了早期再生过程中的细胞迁移动力学。我们的研究揭示了几种假定的细胞类型的迁移,其中包括一种与已发表的关于肘状成瘤细胞的描述非常相似的细胞,这种细胞类型根据“静态射击”研究被认为具有迁徙性,并且长期以来被认为与此类细胞的再生成功有关。结论结合基于神经毒素的麻痹,活体固定技术和耐饥饿研究系统,我们获得了无脊椎动物中最全面的前,后再生的最高分辨率高分辨率纵向记录,并能够检测和鉴定经历广泛分化的几种细胞类型在此过程中迁移。我们希望这里介绍的河豚毒素麻痹和延时成像方法在研究其他动物方面具有广泛的用途,对研究胚胎后的发育特别有价值。

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