Pulmonary expression of early growth response-1: biphasic time course and effect of oxygen concentration
1 Departments of Surgery, Medicine, and Physiology and Cellular Biophysics, College of Physicians and Surgeons of Columbia University, New York, New York 10032; 2 Department of Pathology, The University of New Mexico School of Medicine, Albuquerque, New Mexico 87131; and 3 Department of Immunolog...
Saved in:
Published in | Journal of applied physiology (1985) Vol. 88; no. 6; pp. 2303 - 2309 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Am Physiological Soc
01.06.2000
American Physiological Society |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | 1 Departments of Surgery, Medicine, and
Physiology and Cellular Biophysics, College of Physicians and Surgeons
of Columbia University, New York, New York 10032;
2 Department of Pathology, The
University of New Mexico School of Medicine, Albuquerque, New
Mexico 87131; and 3 Department of
Immunology and Vascular Biology, Scripps Research Institute, La Jolla,
California 92037
Hypoxia
induces complex adaptive responses. In this report, induction of early
growth response-1 (Egr-1) transcripts in lungs of mice
subjected to hypoxia is shown to be dose and time
dependent. Within 30 min of hypoxia, Egr-1
transcripts were ~20-fold elevated in 6% oxygen, ~5.2-fold
increased by 10% oxygen, and returned to the normoxic baseline by 12%
oxygen. Time course studies up to 48 h showed a biphasic profile with
an initial steep rise in Egr-1 transcripts after 0.5 h of hypoxia and a
second elevation beginning after 20-24 h. Hypoxic induction of
Egr-1 was paralleled by enhanced expression of the downstream target
gene tissue factor. Egr-1 and tissue factor antigen were visualized in
bronchial and vascular smooth muscle and in alveolar macrophages. Egr-1
has the capacity to modulate expression of genes involved in the
remodeling of the extracellular matrix and properties of smooth muscle,
thus possibly contributing to the pulmonary response to chronic hypoxia.
transcription factor; hypoxia gene expression; Sp1; tissue factor |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 8750-7587 1522-1601 |
DOI: | 10.1152/jappl.2000.88.6.2303 |