Romay-Tallon Raquel, Rivera-Baltanas Tania, Allen Josh, Olivares Jose M, Kalynchuk Lisa E, Caruncho Hector J
College of Pharmacy and Nutrition, University of Saskatchewan, 107 Wiggins Road, Saskatoon, SK S7N 5E5 Canada.
Neuroscience Cluster, University of Saskatchewan, Saskatoon, Canada.
Biomark Res. 2017 Sep 22;5:27. doi: 10.1186/s40364-017-0107-6. eCollection 2017.
The pattern of serotonin transporter clustering on the plasma membrane of lymphocytes extracted from human whole blood samples has been identified as a putative biomarker of therapeutic efficacy in major depression. Here we evaluated the possibility of performing a similar analysis using blood smears obtained from rats, and from control human subjects and depression patients. We hypothesized that we could optimize a protocol to make the analysis of serotonin protein clustering in blood smears comparable to the analysis of serotonin protein clustering using isolated lymphocytes.
Our data indicate that blood smears require a longer fixation time and longer times of incubation with primary and secondary antibodies. In addition, one needs to optimize the image analysis settings for the analysis of smears. When these steps are followed, the quantitative analysis of both the number and size of serotonin transporter clusters on the plasma membrane of lymphocytes is similar using both blood smears and isolated lymphocytes.
The development of this novel protocol will greatly facilitate the collection of appropriate samples by eliminating the necessity and cost of specialized personnel for drawing blood samples, and by being a less invasive procedure. Therefore, this protocol will help us advance the validation of membrane protein clustering in lymphocytes as a biomarker of therapeutic efficacy in major depression, and bring it closer to its clinical application.
从人类全血样本中提取的淋巴细胞质膜上血清素转运体聚集模式已被确定为重度抑郁症治疗效果的一种假定生物标志物。在此,我们评估了使用从大鼠、对照人类受试者和抑郁症患者获取的血涂片进行类似分析的可能性。我们假设能够优化方案,使血涂片中血清素蛋白聚集分析与使用分离淋巴细胞进行的血清素蛋白聚集分析具有可比性。
我们的数据表明,血涂片需要更长的固定时间以及与一抗和二抗更长的孵育时间。此外,需要针对涂片分析优化图像分析设置。遵循这些步骤后,使用血涂片和分离淋巴细胞对淋巴细胞质膜上血清素转运体簇的数量和大小进行定量分析结果相似。
这种新方案的开发将极大地促进合适样本的采集,消除采集血样所需专业人员的必要性和成本,且侵入性更小。因此,该方案将有助于我们推进淋巴细胞中膜蛋白聚集作为重度抑郁症治疗效果生物标志物的验证,并使其更接近临床应用。