Institute for Pharmaceutical Biology and Phytochemistry, University of Münster, Germany.
Institute for Pharmaceutical Biology and Phytochemistry, University of Münster, Germany.
J Struct Biol. 2019 Nov 1;208(2):174-181. doi: 10.1016/j.jsb.2019.08.013. Epub 2019 Aug 30.
Assessing the internal morphology of Caenorhabditis elegans by a topographical technique like atomic force microscopy (AFM) is a challenging process. As a prerequisite for a successful image acquisition, direct contact between the structure of interest and the AFM probe needs to be established. To gain this insight into the morphology of cuticle and intestine in C. elegans before and after treatment with a tannin-enriched hydro-ethanolic extract from Combretum mucronatum, we developed an approach based on polyethylene glycol embedding, ultra-sectioning, de-embedding and hexamethyldisilazane-dehydration prior to measuring in ambient conditions by intermittent contact mode AFM. The used experimental protocol allowed a facile and fast insight into the ultrastructure of treated versus untreated C. elegans individuals, directly leading to the identification of treatment-associated morphological alterations in the cuticle but not the intestine of C. elegans. Additionally, the presented ultra-microtomy based protocol could allow future insight into virtually any tissue or organism by AFM.
通过原子力显微镜(AFM)等形貌技术评估秀丽隐杆线虫的内部形态是一个具有挑战性的过程。作为成功获取图像的前提条件,需要建立感兴趣的结构与 AFM 探针之间的直接接触。为了在使用富含单宁的 Combretum mucronatum 水-乙醇提取物处理前后深入了解秀丽隐杆线虫的表皮和肠道形态,我们开发了一种基于聚乙二醇包埋、超薄切片、去包埋和六甲基二硅氮烷脱水的方法,然后在环境条件下通过间歇接触模式 AFM 进行测量。所使用的实验方案允许我们轻松、快速地了解处理过的和未处理的秀丽隐杆线虫个体的超微结构,直接导致我们识别出与处理相关的秀丽隐杆线虫表皮的形态变化,但不是肠道的形态变化。此外,所提出的基于超薄切片的方案将来可能通过 AFM 深入了解几乎任何组织或生物体。