Lakowicz J R, Sheppard J R
Am J Hum Genet. 1981 Mar;33(2):155-65.
Using fluorescence spectroscopic methods, we compared the membrane properties of intact fibroblasts from both normal subjects and patients with Huntington disease (HD). Cells were stained with various fluorophores, including 1-anilino-8-naphthalene sulfonic acid (ANS), 2-toluidinyl-6-naphthalene sulfonic acid (TNS), 1,6-diphenyl-1,3,5-hexatriene (DPH), and 6-lauroyl-2-(dimethylamino)-naphthalene (LAURDAN). Using these labeled cells, we measured fluorescence yields and emission maxima (ANS, TNS, and LAURDAN), polarizations (TNS, DPH, and LAURDAN), lifetimes (TNS), and differential polarized lifetimes (DPH). In each instance, comparisons were made between cells from normal and from HD individuals. These cultures were controlled for passage number in culture and for age of donor. We found no significant differences between the HD and the control fibroblasts in experiments using the above-mentioned probes and spectroscopic parameters.
我们使用荧光光谱法比较了正常受试者和亨廷顿病(HD)患者完整成纤维细胞的膜特性。细胞用各种荧光团染色,包括1-苯胺基-8-萘磺酸(ANS)、2-甲苯胺基-6-萘磺酸(TNS)、1,6-二苯基-1,3,5-己三烯(DPH)和6-月桂酰基-2-(二甲基氨基)萘(LAURDAN)。使用这些标记细胞,我们测量了荧光产率和发射最大值(ANS、TNS和LAURDAN)、偏振(TNS、DPH和LAURDAN)、寿命(TNS)和差分偏振寿命(DPH)。在每种情况下,都对正常个体和HD个体的细胞进行了比较。这些培养物在培养中的传代次数和供体年龄方面进行了控制。我们发现在使用上述探针和光谱参数的实验中,HD成纤维细胞和对照成纤维细胞之间没有显著差异。