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急性缺血性脑卒中患者中 CXCR7+ 和 CXCR4+ 干细胞及神经元特异性烯醇化酶。

CXCR7+ and CXCR4+ stem cells and neuron specific enolase in acute ischemic stroke patients.

机构信息

Department of Adult Neurology, Medical University of Gdańsk & University Clinical Centre, Poland.

Department of Clinical Immunology and Transplantology, Medical University of Gdańsk, Poland.

出版信息

Neurochem Int. 2018 Nov;120:134-139. doi: 10.1016/j.neuint.2018.08.009. Epub 2018 Aug 17.

DOI:10.1016/j.neuint.2018.08.009
PMID:30125595
Abstract

Stroke causes an efflux of various groups of progenitor/stem cells from bone marrow to bloodstream and a rise in neuron specific enolase (NSE) serum concentrations. The aim of this study was to identify activity of chosen stem/progenitor cells during first 7 days after stroke through correlations between these cells levels and NSE values. Additional goal was to confirm the role of NSE as a prognostic marker of ischemic stroke. Venous blood was collected repeatedly from 67 acute ischemic stroke patients and 15 control subjects, in order to assess NSE with ELISA, and CD45CD34  CD271+, CD45CD34 + CXCR4+, CD45CD34 + CXCR7+ and CD45CD34  CD133 + stem/progenitor cells by means of flow cytometry. Patients underwent repeated assessment with the National Ischemic Stroke Scale and modified Rankin Scale. Ischemic lesion volumes were assessed twice by MRI-DWI (day 1 and 5 ± 2). NSE correlated negatively with MFI levels of the CD45CD34 + CXCR7+ cells, and percentage levels of the CD45CD34  and CD45CD34 + CXCR4+ cells. NSE concentrations were significantly higher in patients compared to control subjects. NSE on day 2 positively correlated with lesion volume on both MRI. NSE on day 2 and 6-7 correlated positively with initial NIHSS scores, and on day 1 with mRS score on day 9. In conclusion, in this study NSE indicated some activity of the CD45CD34 + CXCR7+, CD45CD34  and CD45CD34 + CXCR4+ stem/progenitor cells in the first 7 days after ischemic stroke. Additionally, this study supports the thesis that NSE might be a valuable prognostic marker in acute ischemic stroke.

摘要

中风会导致各种祖细胞/干细胞从骨髓流出到血液中,并导致神经元特异性烯醇化酶(NSE)血清浓度升高。本研究的目的是通过这些细胞水平与 NSE 值之间的相关性,在中风后 7 天内确定选择的干细胞/祖细胞的活性。另一个目的是确认 NSE 作为缺血性中风预后标志物的作用。从 67 名急性缺血性中风患者和 15 名对照者中反复采集静脉血,以酶联免疫吸附试验(ELISA)评估 NSE,并通过流式细胞术评估 CD45CD34+CD271+、CD45CD34+CXCR4+、CD45CD34+CXCR7+和 CD45CD34+CD133+干细胞/祖细胞。患者接受了国家缺血性中风量表和改良 Rankin 量表的重复评估。通过 MRI-DWI 在第 1 天和第 5 天(±2 天)两次评估缺血性病变体积。NSE 与 CD45CD34+CXCR7+细胞的 MFI 水平呈负相关,与 CD45CD34+和 CD45CD34+CXCR4+细胞的百分比水平呈负相关。与对照组相比,NSE 在患者中的浓度明显更高。第 2 天的 NSE 与 MRI 上的病变体积呈正相关。第 2 天和第 6-7 天的 NSE 与初始 NIHSS 评分呈正相关,第 1 天的 NSE 与第 9 天的 mRS 评分呈正相关。总之,在本研究中,NSE 表明在缺血性中风后 7 天内,CD45CD34+CXCR7+、CD45CD34+和 CD45CD34+CXCR4+干细胞/祖细胞有一定的活性。此外,本研究支持 NSE 可能是急性缺血性中风有价值的预后标志物的观点。

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