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Mitochondria-dependent signalling pathway are involved in the early process of radiation-induced bystander effects
Bystander effects induced by cytoplasmic irradiation have been reported recently. However, the mechanism(s) underlying, such as the functional role of mitochondria, is not clear. In the present study, we used either mtDNA-depleted ( ρ 0 ) A L or normal ( ρ + ) A L cells as irradiated donor cells and...
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Published in: | British journal of cancer 2008-06, Vol.98 (11), p.1839-1844 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Bystander effects induced by cytoplasmic irradiation have been reported recently. However, the mechanism(s) underlying, such as the functional role of mitochondria, is not clear. In the present study, we used either mtDNA-depleted (
ρ
0
) A
L
or normal (
ρ
+
) A
L
cells as irradiated donor cells and normal human skin fibroblasts as receptor cells in a series of medium transfer experiments to investigate the mitochondria-related signal process. Our results indicated that mtDNA-depleted cells or normal A
L
cells treated with mitochondrial respiratory chain function inhibitors had an attenuated
γ
-H2AX induction, which indicates that mitochondria play a functional role in bystander effects. Moreover, it was found that treatment of normal A
L
donor cells with specific inhibitors of NOS, or inhibitor of mitochondrial calcium uptake (ruthenium red) significantly decreased
γ
-H2AX induction and that radiation could stimulate cellular NO and O
2
•−
production in irradiated
ρ
+
A
L
cells, but not in
ρ
0
A
L
cells. These observations, together with the findings that ruthenium red treatment significantly reduced the NO and O
2
•−
levels in irradiated
ρ
+
A
L
cells, suggest that radiation-induced NO derived from mitochondria might be an intracellular bystander factor and calcium-dependent mitochondrial NOS might play an essential role in the process. |
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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/sj.bjc.6604358 |