用咪唑-锇(C3H4N2/OsO4)染色吸血蜱(蜱螨目:伊蚊科)雌蜱唾液腺组织切片的脂质

IF 1.1 Q3 BIOLOGY
M.C. Pereira, E.F. Nodari, L.A. Anholeto, M.I. Camargo-Mathias
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引用次数: 1

摘要

在无脊椎动物组织学中用于脂质染色的组织学技术有时无法证明细胞中这些元素的存在,一旦这些方法留下残留的背景,使得脂质从剩余的细胞质内容物中分离出来变得困难。在透射电子显微镜(TEM)中使用咪唑锇是很常见的,它提供了非常准确的脂质标记。为了优化组织化学分析,本研究提出了一种使用咪唑-锇技术的脂质染色方案,改进后可以在光镜下观察组织学切片中的脂质。本实验采用1%和2%浓度的咪唑锇对血鼻蜱(Rhipicephalus sanguineus sensu lato)的唾液腺切片进行处理。结果表明,这两种浓度都可以准确地检测细胞、细胞膜和质膜中的脂质含量。此外,在这里观察到不同的染色强度,根据不同的喂养周期(2,4和6天),一旦唾液腺分泌周期发生变化。与1%咪唑锇浓度的细胞相比,2%咪唑锇浓度的细胞在脂质染色强度上表现出更大的变化,这表明该方法在常规光学显微镜下可以作为分析无脊椎动物细胞和组织的有效替代方法,与其他技术相比,提供了更清晰和更具体的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of imidazole-osmium (C3H4N2/OsO4) to stain lipids in salivary gland histological sections of Rhipicephalus sanguineus sensu lato (Acari: Ixodidae) female ticks

Histological techniques used to stain lipids in invertebrate histology are sometimes inefficient to demonstrate the presence of these elements in cells, once these methods leave a residual background, making the separation of lipid from the remaining cytoplasmic content difficult. The use of imidazole-osmium is common in transmission electron microscopy (TEM), and it has provided very accurate label of the lipid. Aiming to optimize histochemical analyses, this study proposes a lipid staining protocol using the imidazole-osmium technique, modified to allow the observation of lipids in histological sections under light microscopy. In this experiment, two concentrations of imidazole-osmium (1% and 2%) were applied in salivary glands sections from Rhipicephalus sanguineus sensu lato (s.l.) ticks. The results showed that both concentrations allow accurate detection of the lipid content in cells, in the endomembranes in general and in the plasma membrane as well. In addition, different staining intensities were observed here, varying according to the different feeding periods (2, 4 and 6 days), once the salivary glands undergo alterations in the secretory cycle. The cells submitted to the concentration of 2% imidazole-osmium displayed a greater variation in the lipid staining intensity when compared with those exposed to 1%, indicating that this methodology under conventional light microscopy can be pointed as an efficient alternative for the analysis of invertebrate cells and tissues, providing clearer and more specific results in comparison with other techniques.

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