Erythropoietin and erythropoietin receptors in human CNS neurons, astrocytes, microglia, and oligodendrocytes grown in culture

被引:247
作者
Nagai, A
Nakagawa, E
Choi, HB
Hatori, K
Kobayashi, S
Kim, SU
机构
[1] Univ British Columbia, Dept Med, Div Neurol, Vancouver, BC V6T 1W5, Canada
[2] Shimane Med Univ, Dept Internal Med 3, Izumo, Shimane 693, Japan
[3] Ajou Univ, Brain Dis Res Ctr, Suwon 441749, South Korea
关键词
erythropoietin; human astrocyte; neurotrophic effect; proinflammatory cytokine;
D O I
10.1093/jnen/60.4.386
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Erythropoietin (EPO) is a hematopoietic growth factor that stimulates proliferation and differentiation of erythroid precursor cells and is also known to exert neurotrophic activity in the central nervous system (CNS). However, little is known about expression of EPO and EPO receptor (EPOR) in human CNS tissues. In the present study, we investigated the effects of proinflammatory cytokines on EPO and EPOR expression in highly purified cultures of human neurons, astrocytes, microglia, and oligodendrocytes using reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA). EPO mRNA was demonstrated only in human astrocytes, while EPOR expression was found in human neurons, astrocytes, and microglia. Neither EPO nor EPOR expression was found in oligodendrocytes. In human astrocytes, EPO mRNA and secreted EPO protein levels were downregulated after exposure to proinflammatory cytokines (IL-1 beta, IL-6, or TNF-alpha). In human neurons, TNF-alpha treatment markedly increased EPOR expression. These results suggest that proinflammatory cytokines regulate expression of EPO and EPOR in human neurons, astrocytes, and microglia and further facilitate interactions among different cell types in the human CNS.
引用
收藏
页码:386 / 392
页数:7
相关论文
共 31 条
[1]  
Balasingam V, 1996, J NEUROSCI, V16, P2945
[2]   EXPRESSION OF THE ERYTHROPOIETIN GENE [J].
BERU, N ;
MCDONALD, J ;
LACOMBE, C ;
GOLDWASSER, E .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (07) :2571-2575
[3]  
ERCOLANI L, 1988, J BIOL CHEM, V263, P15335
[4]   DISTINCT SIGNALING PATHWAYS MEDIATE PHORBOL-ESTER-INDUCED AND CYTOKINE-INDUCED INHIBITION OF ERYTHROPOIETIN GENE-EXPRESSION [J].
FANDREY, J ;
HUWILER, A ;
FREDE, S ;
PFEILSCHIFTER, J ;
JELKMANN, W .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 226 (02) :335-340
[5]  
FAQUIN WC, 1992, BLOOD, V79, P1987
[6]   Erythropoietin gene expression is suppressed after lipopolysaccharide or interleukin-1 beta injections in rats [J].
Frede, S ;
Fandrey, J ;
Pagel, H ;
Hellwig, T ;
Jelkmann, W .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 273 (03) :R1067-R1071
[7]   REGULATION OF THE ERYTHROPOIETIN GENE - EVIDENCE THAT THE OXYGEN SENSOR IS A HEME PROTEIN [J].
GOLDBERG, MA ;
DUNNING, SP ;
BUNN, HF .
SCIENCE, 1988, 242 (4884) :1412-1415
[8]   Interleukin-1β and tumor necrosis factor-α stimulate DNA binding of hypoxia-inducible factor-1 [J].
Hellwig-Bürgel, T ;
Rutkowski, K ;
Metzen, E ;
Fandrey, J ;
Jelkmann, W .
BLOOD, 1999, 94 (05) :1561-1567
[9]   MONOKINES INHIBITING ERYTHROPOIETIN PRODUCTION IN HUMAN HEPATOMA CULTURES AND IN ISOLATED PERFUSED RAT KIDNEYS [J].
JELKMANN, W ;
PAGEL, H ;
WOLFF, M ;
FANDREY, J .
LIFE SCIENCES, 1992, 50 (04) :301-308
[10]   ERYTHROPOIETIN - STRUCTURE, CONTROL OF PRODUCTION, AND FUNCTION [J].
JELKMANN, W .
PHYSIOLOGICAL REVIEWS, 1992, 72 (02) :449-489