We studied the in vivo persistence of hypoxia-inducible factor-1a (HIF-1a), main transducer of hypoxia, the differential response in organs exposed to the same degree of hypoxemia and the relationship with apoptosis. We measured HIF-1a (immunohistochem. peroxidase and Western blot) and apoptosis (TUNEL) in heart, liver, kidney, gastrocnemius, and brain of rats exposed to chronic normobaric hypoxia (10% O2) or normoxia (21% O2) for 2 wk. Despite same arterial O2 pressure and increased Hb concn. (219+-5 vs. 124+-4 g/L), the organs responded differently. While marked in brain, muscle, and kidney cortex, HIF-1a was undetectable in heart and liver. In kidney medulla, HIF-1a was high in both normoxia and hypoxia. By contrast, apoptosis was marked in heart, slight in kidney medulla, and undetectable in other organs. We conclude that the HIF-1a response to chronic hypoxia can be a sustained phenomenon, but not in all organs, and that apoptosis responds differently from HIF-1a.
Chronic in vivo hypoxia in various organs: Hypoxia-inducible factor-1a and apoptosis / P.R.M. Bianciardi, M. Fantacci, A. Caretti, R. Ronchi, G. Milano, S. Morel, L. Von Segesser, A. Corno, M. Samaja. - In: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. - ISSN 0006-291X. - 342:3(2006), pp. 875-880.
Chronic in vivo hypoxia in various organs: Hypoxia-inducible factor-1a and apoptosis
P.R.M. BianciardiPrimo
;M. FantacciSecondo
;A. Caretti;R. Ronchi;M. SamajaUltimo
2006
Abstract
We studied the in vivo persistence of hypoxia-inducible factor-1a (HIF-1a), main transducer of hypoxia, the differential response in organs exposed to the same degree of hypoxemia and the relationship with apoptosis. We measured HIF-1a (immunohistochem. peroxidase and Western blot) and apoptosis (TUNEL) in heart, liver, kidney, gastrocnemius, and brain of rats exposed to chronic normobaric hypoxia (10% O2) or normoxia (21% O2) for 2 wk. Despite same arterial O2 pressure and increased Hb concn. (219+-5 vs. 124+-4 g/L), the organs responded differently. While marked in brain, muscle, and kidney cortex, HIF-1a was undetectable in heart and liver. In kidney medulla, HIF-1a was high in both normoxia and hypoxia. By contrast, apoptosis was marked in heart, slight in kidney medulla, and undetectable in other organs. We conclude that the HIF-1a response to chronic hypoxia can be a sustained phenomenon, but not in all organs, and that apoptosis responds differently from HIF-1a.Pubblicazioni consigliate
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