TRANSCRIPTION AND TRANSLATION OF INDUCIBLE NITRIC-OXIDE SYNTHASE IN THE PANCREAS OF PREDIABETIC BB RATS

被引:141
作者
KLEEMANN, R
ROTHE, H
KOLBBACHOFEN, V
XIE, QW
NATHAN, C
MARTIN, S
KOLB, H
机构
[1] UNIV DUSSELDORF,INST IMMUNOBIOL,D-40225 DUSSELDORF,GERMANY
[2] CORNELL UNIV,MED CTR,COLL MED,DEPT MED,NEW YORK,NY 10021
关键词
DIABETES TYPE-1; BB RAT; INSULITIS; NO SYNTHASE; NITRIC OXIDE;
D O I
10.1016/0014-5793(93)80954-S
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 inducible NO synthase (iNOS) was found to be expressed in pancreatic lesions of adult diabetes-prone BB rats. Pancreatic iNOS mRNA was detected by reverse transcriptase PCR in pancreatic RNA of adult diabetes-prone BB rats but not in normal Wistar rats, young diabetes-prone BB rats without insulitis or in diabetes-resistant BB rats. Immunohistochemistry of pancreatic sections using an iNOS-specific antiserum labeled the pancreas of adult diabetes-prone BB rats but not Wistar rats. Parallel staining for ED1-positive macrophages showed restriction of iNOS expression to areas of islet infiltration by macrophages. In conclusion, the data provide direct evidence for enhanced expression of inducible NO synthase in tissue lesions during the development of autoimmune diabetes.
引用
收藏
页码:9 / 12
页数:4
相关论文
共 20 条
[1]   CYTOTOXIC ACTION OF IL-1-BETA AGAINST PANCREATIC-ISLETS IS MEDIATED VIA NITRIC-OXIDE FORMATION AND IS INHIBITED BY N(G)-MONOMETHYL-L-ARGININE [J].
BERGMANN, L ;
KRONCKE, KD ;
SUSCHEK, C ;
KOLB, H ;
KOLBBACHOFERN, V .
FEBS LETTERS, 1992, 299 (01) :103-106
[2]   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
[3]  
CORBETT JA, 1991, J BIOL CHEM, V266, P21351
[4]   INTERLEUKIN-1-BETA INDUCES THE FORMATION OF NITRIC-OXIDE BY BETA-CELLS PURIFIED FROM RODENT ISLETS OF LANGERHANS - EVIDENCE FOR THE BETA-CELL AS A SOURCE AND SITE OF ACTION OF NITRIC-OXIDE [J].
CORBETT, JA ;
WANG, JL ;
SWEETLAND, MA ;
LANCASTER, JR ;
MCDANIEL, ML .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2384-2391
[5]  
JANSSENS SP, 1992, J BIOL CHEM, V267, P14519
[6]  
JIANG Z, 1991, J IMMUNOL, V146, P2990
[7]  
KANTWERK G, 1987, CLIN EXP IMMUNOL, V70, P585
[8]   INVIVO EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE IN EXPERIMENTALLY INDUCED NEUROLOGIC DISEASES [J].
KOPROWSKI, H ;
ZHENG, YM ;
HEBERKATZ, E ;
FRASER, N ;
RORKE, L ;
FU, ZF ;
HANLON, C ;
DIETZSCHOLD, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :3024-3027
[9]   ACTIVATED MACROPHAGES KILL PANCREATIC SYNGENEIC ISLET CELLS VIA ARGININE-DEPENDENT NITRIC-OXIDE GENERATION [J].
KRONCKE, KD ;
KOLBBACHOFEN, V ;
BERSCHICK, B ;
BURKART, V ;
KOLB, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (03) :752-758
[10]   CYTOTOXICITY OF ACTIVATED RAT MACROPHAGES AGAINST SYNGENEIC ISLET CELLS IS ARGININE-DEPENDENT, CORRELATES WITH CITRULLINE AND NITRITE CONCENTRATIONS AND IS IDENTICAL TO LYSIS BY THE NITRIC-OXIDE DONOR NITROPRUSSIDE [J].
KRONCKE, KD ;
RODRIGUEZ, ML ;
KOLB, H ;
KOLBBACHOFEN, V .
DIABETOLOGIA, 1993, 36 (01) :17-24