Maine Medical Center Research Institute, MaineHealth, Scarborough, Maine, USA.
Department of Biological Sciences, University of Southern Maine, Portland, Maine, USA.
J Vasc Res. 2022;59(1):43-49. doi: 10.1159/000517178. Epub 2021 Nov 4.
Quantification of adipocyte size and number is routinely performed for white adipose tissues using existing image analysis software. However, thermogenic adipose tissue has multilocular adipocytes, making it difficult to distinguish adipocyte cell borders and to analyze lipid proportion using existing methods. We developed a simple, standardized method to quantify lipid content of mouse thermogenic adipose tissue. This method, using FIJI analysis of hematoxylin/eosin stained sections, was highly objective and highly reproducible, with ∼99% inter-rater reliability. The method was compared to direct lipid staining of adipose tissue, with comparable results. We used our method to analyze perivascular adipose tissue (PVAT) from C57BL/6 mice on a normal chow diet, compared to calorie restriction or a high fat diet, where lipid storage phenotypes are known. Results indicate that lipid content can be estimated within mouse PVAT in a quantitative and reproducible manner, and shows correlation with previously studied molecular and physiological measures.
定量分析白色脂肪组织中的脂肪细胞大小和数量通常使用现有的图像分析软件进行。然而,产热脂肪组织中的脂肪细胞具有多房性,这使得使用现有的方法难以区分脂肪细胞边界和分析脂质比例。我们开发了一种简单、标准化的方法来定量分析小鼠产热脂肪组织中的脂质含量。该方法使用 FIJI 分析苏木精/伊红染色切片,具有高度的客观性和可重复性,组内相关系数约为 99%。该方法与直接脂肪染色的结果具有可比性。我们使用该方法分析了正常饮食的 C57BL/6 小鼠的血管周脂肪组织(PVAT),并与热量限制或高脂肪饮食进行了比较,因为后者的脂肪存储表型是已知的。结果表明,可以以定量和可重复的方式估计小鼠 PVAT 中的脂质含量,并且与之前研究的分子和生理测量结果相关。