Department of Anatomy, Cell Biology, and Physiology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Physiol Rep. 2022 Feb;10(3):e15167. doi: 10.14814/phy2.15167.
Label-free fluorescence imaging of kidney sections can provide important morphological information, but its utility has not been tested in a histology processing workflow. We tested the feasibility of label-free imaging of paraffin-embedded sections without deparaffinization and its potential usefulness in generating actionable data. Kidney tissue specimens were obtained during percutaneous nephrolithotomy or via diagnostic needle biopsy. Unstained non-deparaffinized sections were imaged using widefield fluorescence microscopy to capture endogenous fluorescence. Some samples were also imaged with confocal microscopy and multiphoton excitation to collect second harmonic generation (SHG) signal to obtain high-quality autofluorescence images with optical sectioning. To adjudicate the label-free signal, the samples or corresponding contiguous sections were subsequently deparaffinized and stained with Lillie's allochrome. Label-free imaging allowed the recognition of various kidney structures and enabled morphological qualification for adequacy. SHG and confocal imaging yielded quantifiable high-quality images for tissue collagens and revealed specific patterns in glomeruli and various tubules. Disease specimens from patients with diabetic kidney disease and focal segmental glomerulosclerosis showed distinctive signatures compared to specimens from healthy controls with normal kidney function. Quantitative cytometry could also be performed when DAPI is added in situ before imaging. These results show that label-free imaging of non-deparaffinized sections provides useful information about tissue quality that could be beneficial to nephropathologists by maximizing the use of scarce kidney tissue. This approach also provides quantifiable features that could inform on the biology of health and disease.
对未经脱蜡处理的石蜡包埋切片进行无标记荧光成像可以提供重要的形态学信息,但尚未在组织学处理流程中对其进行测试。我们测试了对未经脱蜡处理的石蜡包埋切片进行无标记成像的可行性,以及其在生成可操作数据方面的潜在用途。肾组织标本取自经皮肾镜取石术或诊断性针吸活检。使用宽场荧光显微镜对未经染色的非脱蜡切片进行成像,以捕获内源性荧光。一些样本还使用共聚焦显微镜和多光子激发进行成像,以收集二次谐波产生 (SHG) 信号,从而获得具有光学切片的高质量自发荧光图像。为了判断无标记信号,随后对样本或相应的连续切片进行脱蜡和 Lillie 异染体染色。无标记成像可以识别各种肾脏结构,并进行形态学充分性评估。SHG 和共聚焦成像产生了可量化的高质量组织胶原图像,并揭示了肾小球和各种肾小管的特定模式。与肾功能正常的健康对照者的标本相比,来自糖尿病肾病和局灶节段性肾小球硬化症患者的疾病标本显示出独特的特征。在成像前原位添加 DAPI 也可以进行定量细胞学分析。这些结果表明,对未经脱蜡处理的切片进行无标记成像可以提供有关组织质量的有用信息,通过最大限度地利用稀缺的肾组织,这对肾脏病学家可能是有益的。这种方法还提供了可量化的特征,可以为健康和疾病的生物学提供信息。