The Effect of Transcatheter Injections on Cell Viability and Cytokine Release of Mononuclear Cells

被引:10
作者
El Khoury, R. [1 ]
Misra, V. [1 ]
Sharma, S. [1 ]
Cox, C. S. [2 ]
Walker, P. [2 ]
Grotta, J. C. [1 ]
Gee, A. [4 ]
Suzuki, S. [3 ]
Savitz, S. I. [1 ]
机构
[1] Univ Texas Houston, Dept Neurol, Houston, TX USA
[2] Univ Texas Houston, Dept Pediat Surg, Houston, TX USA
[3] Univ Texas Houston, Dept Radiol, Houston, TX USA
[4] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
AUTOLOGOUS BONE-MARROW; ACUTE ISCHEMIC-STROKE; THERAPY; TRIALS;
D O I
10.3174/ajnr.A2092
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: Several studies suggest that various types of cellular therapies enhance recovery after stroke in animal models. IA-based delivery of cells to the brain is under investigation for stroke, but it is unknown whether cells are injured as a result of being injected through a catheter or exposed to iodinated contrast medium or solutions containing heparin. MATERIALS AND METHODS: We assessed the effect of catheterization with the Excelsior SL-10 catheter or exposure to heparin or iodine contrast on human bone marrow MNCs. Viability and cell injury were assessed by trypan blue exclusion, caspase-3 activity, and lipid peroxidation. Cellular function of MNCs was assessed by their production and release of VEGF, IL-10, and IGF-1. RESULTS: Flow rates of 10 million cells from 0.5 to 2 mL/min did not alter MNC viability; however, 5 mL/min of MNCs did reduce viability by 19%. Iodine and low-dose heparin exposure did not affect cell viability; however, high-dose heparin was cytotoxic. Catheter delivery at 2 mL/min did not affect levels of VEGF, IL-10, or IGF-1. CONCLUSIONS: MNCs do not appear to be damaged by heparin, iodine contrast, and the Excelsior SL-10 catheter at flow rates up to 2 mL/min. However, higher flow rates did reduce viability, and high-dose heparin did cause cell death.
引用
收藏
页码:1488 / 1492
页数:5
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