Erythropoietin gene expression in human, monkey and murine brain

被引:441
作者
Marti, HH
Wenger, RH
Rivas, LA
Straumann, U
Digicaylioglu, M
Henn, V
Yonekawa, Y
Bauer, C
Gassmann, M
机构
[1] UNIV ZURICH, DEPT NEUROL, SCH MED, CH-8057 ZURICH, SWITZERLAND
[2] UNIV ZURICH, DEPT NEUROSURG, SCH MED, CH-8057 ZURICH, SWITZERLAND
关键词
astrocyte; hypoxia; VEGF; erythropoietin receptor; quantitative RT-PCR;
D O I
10.1111/j.1460-9568.1996.tb01252.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The haematopoietic growth factor erythropoietin is the primary regulator of mammalian erythropoiesis and is produced by the kidney and the liver in an oxygen-dependent manner. We and others have recently demonstrated erythropoietin gene expression in the rodent brain. In this work, we show that cerebral erythropoietin gene expression is not restricted to rodents but occurs also in the primate brain. Erythropoietin mRNA was detected in biopsies from the human hippocampus, amygdala and temporal cortex and in various brain areas of the monkey Macaca mulatta. Exposure to a low level of oxygen led to elevated erythropoietin mRNA levels in the monkey brain, as did anaemia in the mouse brain. In addition, erythropoietin receptor mRNA was detected in all brain biopsies tested from man, monkey and mouse. Analysis of primary cerebral cells isolated from newborn mice revealed that astrocytes, but not microglia cells, expressed erythropoietin. When incubated at 1% oxygen, astrocytes showed >100-fold time-dependent erythropoietin mRNA accumulation, as measured with the quantitative reverse transcription-polymerase chain reaction. The specificity of hypoxic gene induction in these cells was confirmed by quantitative Northern blot analysis showing hypoxic up-regulation of mRNA encoding the vascular endothelial growth factor, but not of other genes. These findings demonstrate that erythropoietin and its receptor are expressed in the brain of primates as they are in rodents, and that, at least in mice, primary astrocytes are a source of cerebral erythropoietin expression which can be up-regulated by reduced oxygenation.
引用
收藏
页码:666 / 676
页数:11
相关论文
共 51 条
[1]   ERYTHROPOIETIN HAS A MITOGENIC AND POSITIVE CHEMOTACTIC EFFECT ON ENDOTHELIAL-CELLS [J].
ANAGNOSTOU, A ;
LEE, ES ;
KESSIMIAN, N ;
LEVINSON, R ;
STEINER, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5978-5982
[2]   ERYTHROPOIETIN RECEPTOR MESSENGER-RNA EXPRESSION IN HUMAN ENDOTHELIAL-CELLS [J].
ANAGNOSTOU, A ;
LIU, ZY ;
STEINER, M ;
CHIN, K ;
LEE, ES ;
KESSIMIAN, N ;
NOGUCHI, CT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3974-3978
[3]   THE BLOOD-BRAIN-BARRIER [J].
BRADBURY, MWB .
EXPERIMENTAL PHYSIOLOGY, 1993, 78 (04) :453-472
[4]  
BREIER G, 1992, DEVELOPMENT, V114, P521
[5]  
BRUNEVAL P, 1993, BLOOD, V81, P1593
[6]   RECOMBINANT-HUMAN-ERYTHROPOIETIN STIMULATES ANGIOGENESIS IN-VITRO [J].
CARLINI, RG ;
REYES, AA ;
ROTHSTEIN, M .
KIDNEY INTERNATIONAL, 1995, 47 (03) :740-745
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]  
CLAFFEY KP, 1992, J BIOL CHEM, V267, P16317
[9]   EXPRESSION CLONING OF THE MURINE ERYTHROPOIETIN RECEPTOR [J].
DANDREA, AD ;
LODISH, HF ;
WONG, GG .
CELL, 1989, 57 (02) :277-285
[10]   LOCALIZATION OF SPECIFIC ERYTHROPOIETIN BINDING-SITES IN DEFINED AREAS OF THE MOUSE-BRAIN [J].
DIGICAYLIOGLU, M ;
BICHET, S ;
MARTI, HH ;
WENGER, RH ;
RIVAS, LA ;
BAUER, C ;
GASSMANN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) :3717-3720