Juratli Mazen A, Menyaev Yulian A, Sarimollaoglu Mustafa, Siegel Eric R, Nedosekin Dmitry A, Suen James Y, Melerzanov Alexander V, Juratli Tareq A, Galanzha Ekaterina I, Zharov Vladimir P
Arkansas Nanomedicine Center, University of Arkansas for Medical Sciences (UAMS), Little Rock, AR, 72205, United States of America.
Department of General and Visceral Surgery, University Hospital Frankfurt, Goethe-University, Frankfurt am Main, Germany.
PLoS One. 2016 May 26;11(5):e0156269. doi: 10.1371/journal.pone.0156269. eCollection 2016.
Thromboembolic events are one of the world's leading causes of death among patients. Embolus or clot formations have several etiologies including paraneoplastic, post-surgery, cauterization, transplantation, or extracorporeal circuits. Despite its medical significance, little progress has been made in early embolus detection, screening and control. The aim of our study is to test the utility of the in vivo photoacoustic (PA) flow cytometry (PAFC) technique for non-invasive embolus detection in real-time. Using in vivo PAFC, emboli were non-invasively monitored in the bloodstream of two different mouse models. The tumor-free mouse model consisted of two groups, one in which the limbs were clamped to produce vessel stasis (7 procedures), and one where the mice underwent surgery (7 procedures). The melanoma-bearing mouse model also consisted of two groups, one in which the implanted tumor underwent compression (8 procedures), and one where a surgical excision of the implanted tumor was performed (8 procedures). We demonstrated that the PAFC can detect a single embolus, and has the ability to distinguish between erythrocyte-rich (red) and leukocyte/platelet-rich (white) emboli in small vessels. We show that, in tumor-bearing mice, the level of circulating emboli was increased compared to tumor-free mice (p = 0.0013). The number of circulating emboli temporarily increased in the tumor-free control mice during vessel stasis (p = 0.033) and after surgical excisions (signed-rank p = 0.031). Similar observations were noted during tumor compression (p = 0.013) and after tumor excisions (p = 0.012). For the first time, it was possible to detect unlabeled emboli in vivo non-invasively, and to confirm the presence of pigmented tumor cells within circulating emboli. The insight on embolus dynamics during cancer progression and medical procedures highlight the clinical potential of PAFC for early detection of cancer and surgery-induced emboli to prevent the fatal thromboembolic complications by well-timed therapy.
血栓栓塞事件是全球患者主要死因之一。栓子或血凝块形成有多种病因,包括副肿瘤性、手术后、烧灼、移植或体外循环。尽管其具有医学重要性,但在早期栓子检测、筛查和控制方面进展甚微。我们研究的目的是测试体内光声(PA)流式细胞术(PAFC)技术用于实时无创栓子检测的实用性。使用体内PAFC,在两种不同小鼠模型的血流中对栓子进行无创监测。无肿瘤小鼠模型分为两组,一组通过夹闭肢体造成血管淤滞(7次操作),另一组小鼠接受手术(7次操作)。荷黑素瘤小鼠模型也分为两组,一组对植入肿瘤进行压迫(8次操作),另一组对植入肿瘤进行手术切除(8次操作)。我们证明PAFC能够检测单个栓子,并且有能力区分小血管中富含红细胞的(红色)栓子和富含白细胞/血小板的(白色)栓子。我们表明,与无肿瘤小鼠相比,荷瘤小鼠循环栓子水平升高(p = 0.0013)。在无肿瘤对照小鼠中,血管淤滞期间(p = 0.033)和手术切除后(符号秩检验p = 0.031)循环栓子数量暂时增加。在肿瘤压迫期间(p = 0.013)和肿瘤切除后(p = 0.012)也观察到类似情况。首次实现了在体内无创检测未标记的栓子,并证实循环栓子中存在色素沉着的肿瘤细胞。对癌症进展和医疗过程中栓子动态的深入了解突出了PAFC在早期检测癌症和手术诱导栓子方面的临床潜力,以便通过及时治疗预防致命的血栓栓塞并发症。