Centre for Reproductive Medicine and Andrology, University of Münster, Münster, Germany.
Biology of Reproduction and Stem Cell Group, Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra, Portugal.
PLoS One. 2018 Nov 20;13(11):e0207786. doi: 10.1371/journal.pone.0207786. eCollection 2018.
Raman Microspectroscopy represents an innovative tool for the assessment of sperm biochemical features otherwise undetectable by routine semen analysis. Previously, it was shown that induced DNA damage can be detected in smeared sperm by this technique. This novel readout may be of value for clinical settings especially if it can be transferred to living cells. Yet, starting with living sperms this study was carried-out using a variety of conditions to disclose the Raman features of sperm nuclei under different hydration conditions and UV exposure. Human sperm were immobilized and Raman spectra were obtained from individual sperm as repeated measurements. To create conditions with controlled DNA damage, sperm samples were exposed to ultraviolet light. Several media were used to evaluate their effect on Raman spectra in aqueous conditions. To substantiate differences between the experimental conditions, the spectra were analyzed by Principal Component Analysis. We observed that spectra of sperm nuclei obtained in different solutions showed a qualitatively unchanged spectral pattern showing the principal signals related to DNA. Evaluating the effect of ultraviolet light generated the finding that spectra representing DNA damage were only observed in dry conditions but not in aqueous medium. Thus, Raman microspectroscopy was successfully applied for sperm analysis in different conditions, among them in live spermatozoa in aqueous solution during the initial measurement, revealing the principle use of this technique. However, implementation of Raman spectroscopy as a technique for clinical sperm analysis and selection may be especially relevant when DNA evaluation can be established using live sperm.
拉曼微光谱分析代表了一种评估精子生化特征的创新工具,这些特征是常规精液分析无法检测到的。此前,已经证明该技术可以检测到涂抹精子中的诱导 DNA 损伤。这种新的检测方法可能对临床应用具有价值,特别是如果它可以应用于活细胞的话。然而,从活精子开始,本研究使用了多种条件来揭示不同水合条件和紫外线暴露下精子核的拉曼特征。将人类精子固定,并对单个精子进行重复测量以获得精子的拉曼光谱。为了创建具有受控 DNA 损伤的条件,将精子样本暴露于紫外线下。使用了几种介质来评估它们在水介质中的对拉曼光谱的影响。为了证实实验条件之间的差异,通过主成分分析对光谱进行了分析。我们观察到,在不同溶液中获得的精子核光谱显示出定性上不变的光谱模式,显示出与 DNA 相关的主要信号,表明在不同溶液中获得的精子核光谱显示出定性上不变的光谱模式,表明与 DNA 相关的主要信号。评估紫外线的影响发现,只有在干燥条件下才能观察到代表 DNA 损伤的光谱,而在水介质中则观察不到。因此,拉曼微光谱分析成功地应用于不同条件下的精子分析,包括在初始测量期间在水介质中的活精子中,揭示了该技术的主要用途。然而,当可以使用活精子进行 DNA 评估时,拉曼光谱作为一种临床精子分析和选择技术的实施可能特别相关。