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Induction of tissue-type plasminogen activator and 72-kDa type-IV collagenase by ionizing radiation in rat astrocytes

✍ Scribed by Raymond Sawaya; Philip J. Tofion; Sanjeeva Mohanam; Francis Ali-Oosman; Lance A. Liotta; William G. Stetler-Stevenson; Jasti S. Rao


Publisher
John Wiley and Sons
Year
1994
Tongue
French
Weight
872 KB
Volume
56
Category
Article
ISSN
0020-7136

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✦ Synopsis


Abstract

Radiation‐induced damage in the central nervous system (CNS) is believed to be targeted to glial or endothelial cells or both, although the pathophysiology of the process is still poorly understood. In this study, we irradiated rat astrocytes with single doses of X‐rays and then estimated the levels of tissue plasminogen activator (tPA) and collagenase in serum‐free medium and cell extracts at different times. Fibrin zymography revealed increased levels of intracellular tPA activity at 12 hr after irradiation. Gelatin zymography showed continuously increasing levels of extracellular 72‐kDa type‐IV collagenase after irradiation. Quantitative enzymatic activities by densitometry showed a 3‐to 4‐fold elevation in the level of the intracellular tPA activity at 12 hr and a 5‐to 6‐fold increase in the level of the extracellular 72‐kDa type‐IV collagenase activity at 48 hr. An ELISA with specific antibodies for tPA and 72‐kDa type‐IV collagenase indicated a 5‐fold increase in the level of tPA at 12 hr and a more‐than‐7‐fold increase in the level of 72‐kDa type‐IV collagenase at 48 hr. This study adds considerable credibility to the proposed role of plasminogen activators and type‐IV collagenase in the development of CNS damage after radiotherapy for brain tumors.


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We have identified a novel membrane-type matrix metalloproteinase (MT-MMP) expressed on the cell surface and inducing activation of pro-gelatinase A in vitro. In this study, we further examined the possibility that MT-MMP is the activator of pro-gelatinase A in tumors as well as in vitro. Expression