Boston University, Department of Biomedical Engineering, Boston, Massachusetts 02215, USA.
J Biomed Opt. 2011 Nov;16(11):117002. doi: 10.1117/1.3644911.
Elastic scattering spectroscopy (ESS), in the form of wavelength-dependent backscattering measurements, can be used to monitor apoptosis in cell cultures. Early changes in backscattering upon apoptosis induction are characterized by an overall decrease in spectral slope and begin as early as 10 to 15 min post-treatment, progressing over the next 6 to 8 h. The timescale of early scattering changes is consistent with reports of the onset of apoptotic volume decrease (AVD). Modeling cellular scattering with a fixed distribution of sizes and a decreasing index ratio, as well as an increased contribution of the whole cell to cellular scattering, resulting from increased cytoplasmic density, is also consistent with observed spectral changes. Changes in ESS signal from cells undergoing osmotically-induced volume decrease in the absence of apoptosis were similar, but smaller in magnitude, to those of apoptotic cells. Further, blockage of Cl(-) channels, which blocks AVD and delays apoptosis, blocked the early scattering changes, indicating that the early scattering changes during apoptosis result, at least partially, from AVD. Work continues to identify the additional sources of early spectral scattering changes that result from apoptosis induction.
弹性散射光谱学(ESS)以波长相关的背散射测量的形式,可以用于监测细胞培养物中的细胞凋亡。细胞凋亡诱导后,背散射的早期变化特征是光谱斜率整体下降,最早在处理后 10 到 15 分钟开始,并在接下来的 6 到 8 小时内逐渐发展。早期散射变化的时间尺度与报道的凋亡性体积减小(AVD)的开始时间一致。用固定大小分布和指数比减小以及来自细胞质密度增加的整个细胞对细胞散射的贡献增加来模拟细胞散射,也与观察到的光谱变化一致。在没有细胞凋亡的情况下,渗透压诱导的细胞体积减小引起的 ESS 信号变化与凋亡细胞的变化相似,但幅度较小。此外,阻断 Cl(-)通道(阻止 AVD 和延迟细胞凋亡)阻断了早期散射变化,表明凋亡过程中的早期散射变化至少部分是由 AVD 引起的。目前正在继续识别由细胞凋亡诱导引起的早期光谱散射变化的其他来源。