THE CONTRIBUTION OF INCREASED COLLAGEN-SYNTHESIS TO HUMAN GLOMERULOSCLEROSIS - A QUANTITATIVE-ANALYSIS OF ALPHA-2IV COLLAGEN MESSENGER-RNA EXPRESSION BY COMPETITIVE POLYMERASE CHAIN-REACTION

被引:77
作者
PETEN, EP
STRIKER, LJ
CAROME, MA
ELLIOTT, SJ
YANG, CW
STRIKER, GE
机构
[1] NIDDKD, METAB DIS BRANCH,RENAL CELL BIOL SECT,BLDG 10, RM 3N110, BETHESDA, MD 20892 USA
[2] WALTER REED ARMY MED CTR, DEPT MED, NEPHROL SERV, WASHINGTON, DC 20307 USA
[3] WALTER REED ARMY MED CTR, DEPT CLIN INVEST, WASHINGTON, DC 20307 USA
关键词
D O I
10.1084/jem.176.6.1571
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We previously reported that one of the main components of the sclerotic material in human glomerular diseases was type IV collagen. In this study we examined the contribution of increased synthesis to this process at the gene expression level. Sufficient material has not been available to study type IV collagen synthesis by normal or sclerotic glomeruli in humans. We took advantage of the availability of nephrectomy specimens from patients with renal carcinoma, and of the observation that approximately 50% of these patients develop varying degrees of glomerulosclerosis. We microdissected glomeruli from 10 patients and analyzed them using in situ reverse transcription coupled with polymerase chain reaction (PCR) analyses (in situ RT-PCR). Alpha2IV collagen mRNA, after reverse transcription into cDNA, was detected in all patients and appeared to be increased in those with glomerulosclerosis (n = 5). A competitive PCR assay was developed to quantitate this change. There was an average 3.7-fold increase in glomerular type IV collagen cDNA in patients with significant sclerosis. This change was not due to an increased number of glomerular cells. Thus, glomerulosclerosis in humans is associated with an elevation of glomerular type IV collagen gene expression, suggesting that increased synthesis of type IV collagen may represent one component of this process.
引用
收藏
页码:1571 / 1576
页数:6
相关论文
共 21 条
[1]   RENAL IMMUNOPATHOLOGY IN RENAL-CELL CARCINOMA [J].
BEAUFILS, H ;
PATTE, R ;
AUBERT, P ;
CAMEY, M ;
KUSS, R ;
BARBAGELATTA, M ;
CHOMETTE, G .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1984, 404 (01) :87-97
[2]   ABSOLUTE MESSENGER-RNA QUANTIFICATION USING THE POLYMERASE CHAIN-REACTION (PCR) - A NOVEL-APPROACH BY A PCR AIDED TRANSCRIPT TITRATION ASSAY (PATTY) [J].
BECKERANDRE, M ;
HAHLBROCK, K .
NUCLEIC ACIDS RESEARCH, 1989, 17 (22) :9437-9446
[3]  
Dehoff R.T, 1968, QUANTITATIVE MICROSC, P75
[4]   QUANTITATIVE MEASUREMENT OF MESSENGER-RNAS BY POLYMERASE CHAIN-REACTION [J].
DELIDOW, BC ;
PELUSO, JJ ;
WHITE, BA .
GENE ANALYSIS TECHNIQUES, 1989, 6 (06) :120-124
[5]  
DOI T, 1988, AM J PATHOL, V131, P398
[6]  
DOI T, 1991, J EXP MED, V173, P1287, DOI 10.1084/jem.173.5.1287
[7]   EXPRESSION OF ALPHA-SUBUNITS OF G-PROTEINS IN FAILING HUMAN HEART - A REAPPRAISAL UTILIZING QUANTITATIVE POLYMERASE CHAIN-REACTION [J].
FELDMAN, AM ;
RAY, PE ;
BRISTOW, MR .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1991, 23 (12) :1355-1358
[8]  
FOGEL MA, 1991, AM J PATHOL, V138, P465
[9]  
FUNK CD, 1991, J BIOL CHEM, V266, P12508
[10]   ANALYSIS OF CYTOKINE MESSENGER-RNA AND DNA - DETECTION AND QUANTITATION BY COMPETITIVE POLYMERASE CHAIN-REACTION [J].
GILLILAND, G ;
PERRIN, S ;
BLANCHARD, K ;
BUNN, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) :2725-2729