Ionizing radiation decreases capillary-like structure formation by endothelial cells in vitro

被引:20
作者
Ahmad, Mansur [1 ]
Khurana, Neeria R. [1 ]
Jaberi, Joby E. [1 ]
机构
[1] Univ Minnesota, Sch Dent, Dept Diagnost & Biol Sci, Minneapolis, MN 55455 USA
关键词
endothelial cells; radiation; HUVEC; capillary-like structure formation; tissue engineering;
D O I
10.1016/j.mvr.2006.08.005
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
For successful tissue engineering in surgical radiotherapy patients, irradiated endothelial cells (EC) must form new blood vessels to nourish and build connections with the engineered segment. Therefore, it is critical to understand neovasculogenesis by irradiated EC. The objective of this study was to determine the effects of ionizing radiation on endothelial cell proliferation and capillary-like structures (CLS) formation. Human Umbilical Vein Endothelial Cells (HUVEC) were irradiated with single or fractionated doses of radiation. Proliferation was determined by counting cells. CLS morphology was analyzed from photomicrographs. A single dose of 8 Gy radiation was highly lethal to HUVEC compared to lower dosage. A single dose had more of an inhibitory effect on cell proliferation compared to the same dose delivered in a fractionated manner. CLS formation began after cells reached confluency. To form a CLS, a single cell expanded, and a number of cells rearranged around its periphery in an oval fashion (mimicking a vessel wall). The central cell later disintegrated leaving a void, mimicking the lumen. Irradiated EC can form CLS, although they are fewer and smaller compared to those by sham cells. By disrupting the peripheral cells, >= 4 Gy doses significantly reduced the number of CLS. The disruptive affect was seen more with large CLS compared to small CLS. At different doses, the shapes of CLS were not significantly different. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:14 / 19
页数:6
相关论文
共 36 条
[1]   In vitro model for developmental progression from vasculogenesis to angiogenesis with a murine endothelial precursor cell line, MFLM-4 [J].
Akeson, AL ;
Brooks, SK ;
Thompson, FY ;
Greenberg, JM .
MICROVASCULAR RESEARCH, 2001, 61 (01) :75-86
[2]  
Annabi B, 2003, CANCER BIOL THER, V2, P642
[3]   Effects of multiple doses of ionizing radiation on cytokine expression in rat and human cells [J].
Boerma, M ;
Schutte-Bart, CI ;
Wedekind, LE ;
Beekhuizen, H ;
Wondergem, J .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2003, 79 (11) :889-896
[4]  
Brieger J, 2005, INT J MOL MED, V15, P145
[5]   Glioblastoma cells block radiation-induced programmed cell death of endothelial cells [J].
Brown, CK ;
Khodarev, NN ;
Yu, JQ ;
Moo-Young, T ;
Labay, E ;
Darga, TE ;
Posner, MC ;
Weichselbaum, RR ;
Mauceri, HJ .
FEBS LETTERS, 2004, 565 (1-3) :167-170
[6]   Molecular mechanisms of blood vessel growth [J].
Conway, EM ;
Collen, D ;
Carmeliet, P .
CARDIOVASCULAR RESEARCH, 2001, 49 (03) :507-521
[7]   RADIATION-INDUCED INHIBITION OF HUMAN ENDOTHELIAL CELLS REPLICATING IN CULTURE [J].
DEGOWIN, RL ;
LEWIS, LJ ;
MASON, RE ;
BORKE, MK ;
HOAK, JC .
RADIATION RESEARCH, 1976, 68 (02) :244-250
[8]  
DEGOWIN RL, 1974, J LAB CLIN MED, V84, P42
[9]  
Fernyhough Melinda E, 2003, Methods Cell Sci, V25, P221
[10]   THE IMPLICATIONS OF ANGIOGENESIS FOR THE BIOLOGY AND THERAPY OF CANCER METASTASIS [J].
FIDLER, IJ ;
ELLIS, LM .
CELL, 1994, 79 (02) :185-188