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一种量化再生水螅芽生长的简单方法。

A Simple Method for Quantifying Blastema Growth in Regenerating Planarians.

机构信息

Department of Biology, Swarthmore College, Swarthmore, Pennsylvania.

Department of Physics and Astronomy, Swarthmore College, Swarthmore, Pennsylvania.

出版信息

Curr Protoc. 2023 Mar;3(3):e684. doi: 10.1002/cpz1.684.

Abstract

Due to their strong regenerative capabilities, freshwater planarians are a well-suited model system for studying the effects of chemicals on stem cell biology and regeneration. After amputation, a planarian will regenerate the missing body parts within 1 to 2 weeks. Because planarians have a distinct head morphology that can be easily identified, head and eye regeneration has been a popular qualitative measure of toxicity. However, qualitative measures can only detect strong defects. Here, we present protocols for quantifying the rate of blastema growth to measure regeneration defects for assessment of chemical toxicity. Following amputation, a regenerative blastema forms at the wound site. Over the course of several days, the blastema grows and subsequently re-forms the missing anatomical structures. This growth can be measured by imaging the regenerating planarian. As the blastema tissue is unpigmented, it can be easily distinguished from the remaining pigmented body using standard image analysis techniques. Basic Protocol 1 provides a step-by-step guide for imaging regenerating planarians over several days of regeneration. Basic Protocol 2 describes the necessary steps for the quantification of blastema size using freeware. It is accompanied by video tutorials to facilitate adaptation. Basic Protocol 3 shows how to calculate the growth rate using linear curve fitting in a spreadsheet. The ease of implementation and low cost make this procedure suitable for an undergraduate laboratory teaching setting, in addition to typical research settings. Although we focus on head regeneration in Dugesia japonica, these protocols are adaptable to other wound sites and planarian species. © 2023 Wiley Periodicals LLC. Basic Protocol 1: Imaging planarians during regeneration Basic Protocol 2: Quantitative analysis of blastema size with ImageJ Basic Protocol 3: Quantification of blastema growth rate.

摘要

由于其强大的再生能力,淡水涡虫是研究化学物质对干细胞生物学和再生影响的理想模型系统。在截肢后,涡虫将在 1 到 2 周内再生缺失的身体部位。由于涡虫具有明显的头部形态,很容易识别,头部和眼睛再生一直是毒性的一种常用定性测量方法。然而,定性测量只能检测到强烈的缺陷。在这里,我们提供了量化芽基生长率的方案,以测量再生缺陷,用于评估化学毒性。截肢后,在伤口部位形成再生芽基。在几天的时间里,芽基生长并随后重新形成缺失的解剖结构。可以通过对再生涡虫进行成像来测量这种生长。由于芽基组织没有色素,因此可以使用标准的图像分析技术很容易地将其与剩余的色素化身体区分开来。基本方案 1 提供了在再生的几天内对再生涡虫进行成像的逐步指导。基本方案 2 描述了使用免费软件量化芽基大小的必要步骤。它还附有视频教程,以方便适应。基本方案 3 展示了如何在电子表格中使用线性曲线拟合来计算生长速率。该程序易于实施且成本低廉,除了典型的研究环境外,还适合于本科生实验室教学环境。尽管我们专注于日本涡虫的头部再生,但这些方案适用于其他伤口部位和涡虫物种。 © 2023 Wiley Periodicals LLC. 基本方案 1:在再生过程中对涡虫进行成像 基本方案 2:使用 ImageJ 对芽基大小进行定量分析 基本方案 3:量化芽基生长率。

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本文引用的文献

2
Model systems for regeneration: planarians.再生模型系统:涡虫。
Development. 2019 Sep 11;146(17):dev167684. doi: 10.1242/dev.167684.

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