Theodossiou Anna, Martinez Jocelyn, Walsh Alex J
Texas A&M University, Department of Biomedical Engineering, College Station, Texas, United States.
J Biomed Opt. 2024 Dec;29(12):126501. doi: 10.1117/1.JBO.29.12.126501. Epub 2024 Dec 19.
Cellular metabolic dynamics can occur within milliseconds, yet there are no optimal tools to spatially and temporally capture these events. Autofluorescence imaging can provide metabolic information on the cellular level due to the intrinsic fluorescence of reduced nicotinamide adenine dinucleotide (phosphate) [NAD(P)H] and flavin adenine dinucleotide (FAD).
Our goal is to build and evaluate a widefield microscope optimized for rapid autofluorescence imaging of metabolic changes in cells.
A widefield, fluorescence microscope was assembled from an inverted microscope base, an light-emitting diode (LED) for excitation, and an image splitter for simultaneous but separate imaging of two bandwidths of emission (451/106 and 560/94 nm) on a single scientific complementary metal-oxide-semiconductor (sCMOS) camera. MCF-7 cells and primary murine hippocampal neurons were metabolically perturbed using cyanide and imaged to optimize illumination and camera exposure. To capture a rapid change in metabolism, MCF-7 cells were starved for 1 h and imaged while reintroduced to glucose.
Significant differences in the optical redox ratio (ORR) and intensity of NAD(P)H divided by the summed intensities of NAD(P)H and FAD were quantified for cyanide-treated neurons and MCF-7 cells at illumination powers above 0.30 mW and camera exposures as low as 5 ms; however, low illumination and camera exposures hindered the ability to identify subcellular features. Minimal photobleaching was quantified for 30 s of continuous imaging for illuminations at 4.14 mW and below. Using the optimized illumination power of 4.14 mW and an exposure of 10 ms, continuous autofluorescence imaging of starved MCF-7 cells demonstrated a rapid, yet heterogeneous, increase in the ORR of cells upon exposure to glucose.
Ultimately, this widefield autofluorescence imaging system allowed for dynamic imaging and quantification of cellular metabolism at 99.6 Hz.
细胞代谢动力学能在毫秒内发生,但尚无在空间和时间上捕捉这些事件的理想工具。由于还原型烟酰胺腺嘌呤二核苷酸(磷酸)[NAD(P)H]和黄素腺嘌呤二核苷酸(FAD)的固有荧光,自发荧光成像可在细胞水平提供代谢信息。
我们的目标是构建并评估一台针对细胞代谢变化的快速自发荧光成像进行优化的宽视场显微镜。
一台宽视场荧光显微镜由倒置显微镜底座、用于激发的发光二极管(LED)以及用于在单个科学互补金属氧化物半导体(sCMOS)相机上同时但分别成像两个发射带宽(451/106和560/94纳米)的图像分离器组装而成。使用氰化物对MCF-7细胞和原代小鼠海马神经元进行代谢扰动,并成像以优化照明和相机曝光。为了捕捉代谢的快速变化,将MCF-7细胞饥饿1小时,在重新引入葡萄糖时进行成像。
在照明功率高于0.30毫瓦且相机曝光低至5毫秒的情况下,对经氰化物处理的神经元和MCF-7细胞的光学氧化还原比(ORR)以及NAD(P)H强度除以NAD(P)H和FAD的总强度进行了定量分析;然而,低照明和相机曝光阻碍了识别亚细胞特征的能力。对于4.14毫瓦及以下的照明,连续成像30秒的光漂白量最小。使用4.14毫瓦的优化照明功率和10毫秒的曝光,对饥饿的MCF-7细胞进行连续自发荧光成像显示,细胞在接触葡萄糖后ORR迅速但不均匀地增加。
最终,这个宽视场自发荧光成像系统能够以99.6赫兹的频率对细胞代谢进行动态成像和定量分析。