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Vol. 59, Issue 1, 69-75, January 2001
Division of Pharmacology, College of Pharmacy, The Ohio State
University, Columbus, Ohio
Activation of endothelial cell integrins inhibits DNA breakage by
diverse agents, including the DNA-damaging agent bleomycin. DNA breaks
activate nuclear poly(ADP-ribose) polymerase (PARP), which regulates
chromatin structure and DNA repair. We determined the role of PARP in
suppression of bleomycin genotoxicity by integrins using wild-type and
PARP knockout mouse lung endothelial cells (MLEC), and the PARP
inhibitor, 3-aminobenzamide (3AB). Activation of
1 integrins by
antibody clustering enhanced the sensitivity of wild-type nuclei to
digestion with micrococcal nuclease and deoxyribonuclease I, indicating
that chromatin structure was altered. 3AB blocked this effect. Knockout
and 3AB-treated wild-type MLEC were hypersensitive to deoxyribonuclease
I compared with wild-type cells, demonstrating that PARP regulates
chromatin structure. Integrin clustering reduced the hypersensitivity
of knockout cells, suggesting additional, PARP-independent mechanisms
that inhibit nuclease interaction with chromatin. Bleomycin caused DNA
breakage in wild-type and knockout MLEC. Breaks were eliminated after
60 min incubation of wild-type cells in drug-free medium, whereas 3AB
or PARP knockout inhibited DNA repair. Integrin clustering protected
wild-type cells from DNA breakage, and 3AB and PARP knockout inhibited
this protection. Bleomycin caused large increases in PARP activity in
wild-type but not knockout MLEC, and integrin clustering inhibited the
activation of PARP. The results indicate that the antigenotoxic effects
of integrin activation require PARP and that integrins alter chromatin
structure by PARP-dependent and -independent mechanisms.
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