Production and secretion of adrenomedullin from glial cell tumors and its effects on cAMP production

被引:65
作者
Takahashi, K
Satoh, F
Hara, E
Sone, M
Murakami, O
Kayama, T
Yoshimoto, T
Shibahara, S
机构
[1] TOHOKU UNIV, SCH MED, DEPT MOL BIOL & APPL PHYSIOL, AOBA KU, SENDAI, MIYAGI 98077, JAPAN
[2] TOHOKU UNIV, SCH MED, DEPT INTERNAL MED 2, AOBA KU, SENDAI, MIYAGI 98077, JAPAN
[3] NATL IWATE HOSP, ICHINOSEKI, IWATE 021, JAPAN
关键词
adrenomedullin; glioblastoma; astrocytoma; brain tumor; glia; cytokine;
D O I
10.1016/S0196-9781(97)00186-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The expression of adrenomedullin (ADM) and its mRNA was studied in human glial cell tumors and cultured glioblastoma cell lines, T98G and A172. Northern blot analysis showed that ADM mRNA was expressed in all brain tumors examined (three anaplastic astrocytomas and two glioblastomas multiforme) and in the glioblastoma cell lines. Immunoreactive (IR-) ADM was detectable in these brain tumors by radioimmunoassay (0.31-2.O pmol/g wet weight), except for one anaplastic astrocytoma. Reverse phase high performance liquid chromatography of the tumor extracts showed a single peak eluting in the position of ADM-(1-52). TR-ADM concentrations in the cultured media of T98G cells were 205.5 +/- 8.4 fmol/10(5) cells/24 h (mean +/- SEM, n = 5). Treatment of T98G cells with interferon gamma or interleukin 1 beta increased the expression levels of ADM mRNA and the IR-ADM concentrations in the cultured media, whereas tumor necrosis factor or decreased them in a dose-dependent manner. Treatment with synthetic ADM-(1-52) (10(-8) or 10(-7) mol/l) increased the cAMP concentrations in the cultured media of T98G cells. These findings suggest that ADM is secreted from glial cell rumors and is related to the pathophysiology of these tumors. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:1117 / 1124
页数:8
相关论文
共 37 条
[1]  
ADRIAN TE, 1983, LANCET, V2, P540
[2]   In vitro recordings from area postrema neurons demonstrate responsiveness to adrenomedullin [J].
Allen, MA ;
Ferguson, AV .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1996, 270 (04) :R920-R925
[3]  
CAMPION HC, 1997, AM J PHYSIOL, V272, pR234
[4]   ADRENOMEDULLIN SUPPRESSES MITOGENESIS IN RAT MESANGIAL CELLS VIA CAMP PATHWAY [J].
CHINI, EN ;
CHOI, E ;
GRANDE, JP ;
BURNETT, JC ;
DOUSA, TP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 215 (03) :868-873
[5]  
CUNNINGHAM ET, 1992, J NEUROSCI, V12, P1101
[6]  
FENG CJ, 1994, LIFE SCI, V55, pPL433
[7]   Expression of heme oxygenase and inducible nitric oxide synthase mRNA in human brain tumors [J].
Hara, E ;
Takahashi, K ;
Tominaga, T ;
Kumabe, T ;
Kayama, T ;
Suzuki, H ;
Fujita, H ;
Yoshimoto, T ;
Shirato, K ;
Shibahara, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 224 (01) :153-158
[8]   GENOMIC STRUCTURE OF HUMAN ADRENOMEDULLIN GENE [J].
ISHIMITSU, T ;
KOJIMA, M ;
KANGAWA, K ;
HINO, J ;
MATSUOKA, H ;
KITAMURA, K ;
ETO, T ;
MATSUO, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 203 (01) :631-639
[9]   IDENTIFICATION AND CHARACTERIZATION OF RECEPTORS FOR TUMOR-NECROSIS-FACTOR-ALPHA IN THE BRAIN [J].
KINOUCHI, K ;
BROWN, G ;
PASTERNAK, G ;
DONNER, DB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (03) :1532-1538
[10]   ADRENOMEDULLIN - A NOVEL HYPOTENSIVE PEPTIDE ISOLATED FROM HUMAN PHEOCHROMOCYTOMA [J].
KITAMURA, K ;
KANGAWA, K ;
KAWAMOTO, M ;
ICHIKI, Y ;
NAKAMURA, S ;
MATSUO, H ;
ETO, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 192 (02) :553-560