Expression of hypoxia-inducible factor-1α in the brain of rats during chronic hypoxia

被引:203
作者
Chávez, JC
Agani, F
Pichiule, P
LaManna, JC
机构
[1] Case Western Reserve Univ, Sch Med, Dept Neurol BRB, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Anat, Cleveland, OH 44106 USA
关键词
brain hypoxic adaptation; hypoxia-inducible genes; brain capillary angiogenesis; brain tissue oxygen; vascular endothelial growth factor;
D O I
10.1152/jappl.2000.89.5.1937
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that regulates adaptive responses to the lack of oxygen in mammalian cells. HIF-1 consists of two proteins, HIF-1 alpha and HIF-1 beta. HIF-1 alpha. accumulates under hypoxic conditions, whereas HIF-1 beta is constitutively expressed. HIF-1 alpha. and HIF-1 beta expression were measured during adaptation to hypobaric hypoxia (0.5 atm) in rat cerebral cortex. Western blot analyses indicated that HIF-1 alpha rapidly accumulated during the onset of hypoxia and did not fall for 14 days but fell to normal by 21 days despite the continuous low arterial oxygen tension. Immunostaining showed that neurons, astrocytes, ependymal cells, and possibly endothelial cells were the cell types expressing HIF-1 alpha. Genes with hypoxia-responsive elements were activated under these conditions, as evidenced by elevated vascular endothelial growth factor and glucose transporter-1. mRNA levels. When 21-day-adapted rats were exposed to a more severe hypoxic challenge (8% oxygen), HIF-1 alpha accumulated again. On the basis of these results, we speculate that the vascular remodeling and metabolic changes triggered during prolonged hypoxia are capable of restoring normal tissue oxygen levels.
引用
收藏
页码:1937 / 1942
页数:6
相关论文
共 29 条
[1]   Induction of hypoxia-inducible factor-1 (HIF-1) and its target genes following focal ischaemia in rat brain [J].
Bergeron, M ;
Yu, AY ;
Solway, KE ;
Semenza, GL ;
Sharp, FR .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (12) :4159-4170
[2]   Increased brain capillaries in chronic hypoxia [J].
Boero, JA ;
Ascher, J ;
Arregui, A ;
Rovainen, C ;
Woolsey, TA .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 86 (04) :1211-1219
[3]   Oxygen sensing and molecular adaptation to hypoxia [J].
Bunn, HF ;
Poyton, RO .
PHYSIOLOGICAL REVIEWS, 1996, 76 (03) :839-885
[4]   REDUCED MITOCHONDRIAL RESPIRATION IN MOUSE CEREBRAL-CORTEX DURING CHRONIC HYPOXIA [J].
CHAVEZ, JC ;
PICHIULE, P ;
BOERO, J ;
ALBERTO, A .
NEUROSCIENCE LETTERS, 1995, 193 (03) :169-172
[5]   HIF-1α and p53 promote hypoxia-induced delayed neuronal death in models of CNS ischemia [J].
Halterman, MW ;
Federoff, HJ .
EXPERIMENTAL NEUROLOGY, 1999, 159 (01) :65-72
[6]   Hypoxia-inducible factor-1α mediates hypoxia-induced delayed neuronal death that involves p53 [J].
Halterman, MW ;
Miller, CC ;
Federoff, HJ .
JOURNAL OF NEUROSCIENCE, 1999, 19 (16) :6818-6824
[7]   Time-course and reversibility of the hypoxia-induced alterations in cerebral vascularity and cerebral capillary glucose transporter density [J].
Harik, N ;
Harik, SI ;
Kuo, NT ;
Sakai, K ;
Przybylski, RJ ;
LaManna, JC .
BRAIN RESEARCH, 1996, 737 (1-2) :335-338
[8]   BRAIN GLUCOSE-METABOLISM IN HYPOBARIC HYPOXIA [J].
HARIK, SI ;
LUST, WD ;
JONES, SC ;
LAURO, KL ;
PUNDIK, S ;
LAMANNA, JC .
JOURNAL OF APPLIED PHYSIOLOGY, 1995, 79 (01) :136-140
[9]   HYPOXIA-INDUCED BRAIN ANGIOGENESIS IN THE ADULT-RAT [J].
HARIK, SI ;
HRITZ, MA ;
LAMANNA, JC .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 485 (02) :525-530
[10]   HYPOXIA INCREASES GLUCOSE-TRANSPORT AT BLOOD-BRAIN-BARRIER IN RATS [J].
HARIK, SI ;
BEHMAND, RA ;
LAMANNA, JC .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (02) :896-901