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5 gene
transcription
1 Division of Pulmonary and Critical Care Medicine, Department of Medicine, Veterans Affairs Medical Center and Emory University School of Medicine, Atlanta, Georgia, 30033; and 2 Division of Respiratory and Critical Care Medicine, Washington University School of Medicine, St. Louis, Missouri, 63110
Lung injury is accompanied by increased
deposition of fibronectin (FN) matrices. Activated monocytic cells
recruited to sites of lung injury express integrin receptors for FN
that mediate their interaction with this matrix. One such integrin,
5
1, mediates many of the biological
effects of FN, and its expression may be important for immune cell
function at sites of lung injury. Herein, we examine the expression of
5
1 in response to the tumor promoter phorbol 12-myristate 13-acetate (PMA) in the human promonocytic cell
line U-937. We demonstrate that PMA enhanced the adherence of U-937
cells to FN by increasing the expression of both the
5-
and
1-subunit mRNAs and the surface expression of the
protein. In U-937 cells transfected with an
5 promoter-reporter gene, we found
that PMA induced the transcription of the
5 gene by acting on very specific
promoter sequences other than activator protein-1 in a protein kinase
C-dependent manner. Lipopolysaccharide had a similar effect. Modulation
of
5
1 expression may be important for
regulation of monocytic cell function in lung inflammation after injury.
protein kinase C; transcription factor; promoter; fibronectin; phorbol 12-myristate 13-acetate
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