Polgár Tamás F, Spisák Krisztina, Kádár Zalán, Alodah Nora, Szebeni Gabor J, Klein Kata, Patai Roland, Siklós László, Nógrádi Bernát
Institute of Biophysics, HUN-REN Biological Research Centre, Szeged, Hungary.
Theoretical Medicine Doctoral School, University of Szeged, Szeged, Hungary.
Pathol Oncol Res. 2025 Apr 4;31:1612087. doi: 10.3389/pore.2025.1612087. eCollection 2025.
Photobleaching of immunofluorescence signal is a well-known phenomenon, however, its impact on derived parameters characterizing number and shape of different cell types in tissue sections is less understood. Our aim was to determine whether the duration of illumination and the type of fluorophore (Alexa Fluor 546 (A546), and Alexa Fluor 488 Plus (A488)) can influence the acquired morphometric parameters of cells in the nervous system. Immunofluorescent staining of microglia and neurons was performed on mouse spinal cord sections. Mean color intensity in a field of view, number of detectable neuronal cell profiles, partial coverage of microglial profiles, and fractal geometrical parameters were determined. All measurements were made using epifluorescence microscopy with identical acquisition parameters. Most of the measured parameters suffered significant alternation after 30-60 s of illumination. The data-altering effect of photobleaching was most prominent in the case of mean fluorescent intensity. Thus, while immunofluorescent staining is useful for co-localizing different groups of cells, cell-specific quantitative morphological measurements require photostable staining. Possibility of the combination of these methods on the same section in order to achieve multi-channel localization without photobleaching is exemplified.
免疫荧光信号的光漂白是一种众所周知的现象,然而,其对组织切片中表征不同细胞类型数量和形状的衍生参数的影响却鲜为人知。我们的目的是确定光照持续时间和荧光团类型(Alexa Fluor 546(A546)和Alexa Fluor 488 Plus(A488))是否会影响神经系统中细胞的形态学参数。对小鼠脊髓切片进行了小胶质细胞和神经元的免疫荧光染色。测定了视野中的平均颜色强度、可检测到的神经元细胞轮廓数量、小胶质细胞轮廓的部分覆盖率以及分形几何参数。所有测量均使用具有相同采集参数的落射荧光显微镜进行。在光照30 - 60秒后,大多数测量参数发生了显著变化。光漂白对数据的改变作用在平均荧光强度方面最为显著。因此,虽然免疫荧光染色可用于不同细胞群的共定位,但细胞特异性定量形态学测量需要光稳定染色。文中举例说明了在同一切片上组合这些方法以实现无光漂白的多通道定位的可能性。