Ciencias,UNAM

Increased expression of gelatinases and collagenase in rat lungs exposed to 100% oxygen

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dc.contributor.author Selman, M
dc.contributor.author Ridge, K
dc.contributor.author BarRíos, R
dc.contributor.author Sznajder, JI
dc.contributor.author Pardo-Cemo, Annie
dc.date.accessioned 2011-01-22T10:28:17Z
dc.date.available 2011-01-22T10:28:17Z
dc.date.issued 1996
dc.identifier.issn 1073449X
dc.identifier.uri http://hdl.handle.net/11154/2928
dc.description.abstract Exposure of adult rats to 100% O-2 produces a lethal injury by 72 h. We reasoned that matrix metalloproteinases participate in the pathogenesis of hyperoxic lung injury. To that end we studied the expression and activity of gelatinases A and B and interstitial collagenase in lung tissues and bronchoalveolar ravage fluids (BALF) of rats exposed to 100% oxygen for 60 h. Gelatin zymography of BALF samples revealed a similar to 72 kDa molecular species both in controls and oxygen-exposed animals. In addition, BALF from hyperoxic rats exhibited a 95-kDa gelatinase. Likewise, BALF total gelatinolytic and collagenolytic activities were significantly increased in oxygen-exposed rats. In situ hybridization revealed an increase in type IV collagenases as well as interstitial collagenase mRNAs in the oxygen-exposed lungs. The three enzymes were expressed by alveolar macrophages, and in variable degrees by interstitial and alveolar epithelial cells. Immunoreactive gelatinase B and collagenase paralleled the cell localization of the mRNAs but were also detected in the alveolar walls and interstitium. In situ zymography showed gelatinolytic activity in frozen sections of oxygen-exposed lungs but not in normal lungs. The upregulation of these metalloproteinases during acute exposure to 100% O-2 suggests that they might contribute to hyperoxic lung damage through the degradation of extracellular matrix components. en_US
dc.language.iso en en_US
dc.title Increased expression of gelatinases and collagenase in rat lungs exposed to 100% oxygen
dc.type Artículo de investigación en_US
dc.identifier.idprometeo 3049
dc.source.novolpages 154(4):1067-1075
dc.subject.wos Critical Care Medicine
dc.subject.wos Respiratory System
dc.description.index WoS: SCI, SSCI o AHCI
dc.relation.journal American Journal of Respiratory and Critical Care Medicine
dc.description.Departamento Departamento de Biología Comparada

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