Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland.
Doctoral School of Exact and Natural Sciences, Jagiellonian University, Prof. Stanislawa Lojasiewicza 11, 30-348 Krakow, Poland.
Int J Mol Sci. 2024 Nov 15;25(22):12274. doi: 10.3390/ijms252212274.
Adipocytes derived from 3T3-L1 cells are a gold standard for analyses of adipogenesis processes and the metabolism of fat cells. A widely used histological and immunohistochemical staining and mass spectrometry lipidomics are mainly aimed for examining lipid droplets (LDs). Visualizing other cellular compartments contributing to the cellular machinery requires additional cell culturing for multiple labeling. Here, we present the localization of the intracellular structure of the 3T3-L1-derived adipocytes utilizing vibrational spectromicroscopy, which simultaneously illustrates the cellular compartments and provides chemical composition without extensive sample preparation and in the naïve state. Both vibrational spectra (FTIR-Fourier transform infrared and RS-Raman scattering spectroscopy) extended the gathered chemical information. We proved that both IR and RS spectra provide distinct chemical information about lipid content and their structure. Despite the expected presence of triacylglycerols and cholesteryl esters in lipid droplets, we also estimated the length and unsaturation degree of the fatty acid acyl chains that were congruent with known MS lipidomics of these cells. In addition, the clustering of spectral images revealed that the direct surroundings around LDs attributed to lipid-associated proteins and a high abundance of mitochondria. Finally, by using quantified markers of biomolecules, we showed that the fixative agents, paraformaldehyde and glutaraldehyde, affected the cellular compartment differently. We concluded that PFA preserves LDs better, while GA fixation is better for cytochromes and unsaturated lipid analysis. The proposed analysis of the spectral images constitutes a complementary tool for investigations into the structural and molecular features of fat cells.
3T3-L1 细胞来源的脂肪细胞是分析脂肪生成过程和脂肪细胞代谢的金标准。广泛使用的组织学和免疫组织化学染色以及质谱脂质组学主要针对脂滴 (LDs) 进行检测。要观察对细胞机制有贡献的其他细胞区室,需要进行额外的细胞培养以进行多重标记。在这里,我们利用振动光谱显微镜研究了 3T3-L1 衍生的脂肪细胞的细胞内结构的定位,该方法同时说明了细胞区室并提供了无需广泛的样品制备和在自然状态下的化学组成。两种振动光谱(FTIR-傅里叶变换红外和 RS-Raman 散射光谱)扩展了收集的化学信息。我们证明,IR 和 RS 光谱都提供了有关脂质含量及其结构的独特化学信息。尽管在脂滴中预期存在三酰基甘油和胆固醇酯,但我们还估计了脂肪酸酰基链的长度和不饱和度,这与这些细胞的已知 MS 脂质组学一致。此外,光谱图像的聚类表明,LDs 的直接周围环境归因于与脂质相关的蛋白质和大量线粒体。最后,通过使用生物分子的定量标记物,我们表明固定剂多聚甲醛和戊二醛对细胞区室的影响不同。我们得出结论,PFA 更好地保存 LDs,而 GA 固定更适合细胞色素和不饱和脂质分析。对光谱图像的分析构成了对脂肪细胞结构和分子特征进行研究的补充工具。