High glucose-induced TGF-beta 1 regulates mesangial production of heparan sulfate proteoglycan

被引:62
作者
Kolm, V [1 ]
Sauer, U [1 ]
Olgemoller, B [1 ]
Schleicher, ED [1 ]
机构
[1] UNIV MUNICH, ACAD HOSP, DIABET RES INST, DEPT BIOCHEM, D-80804 MUNICH, GERMANY
来源
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY | 1996年 / 270卷 / 05期
关键词
diabetic nephropathy; transforming growth factor-beta 1 antisense; perlecan; fibronectin; hyperglycemia;
D O I
10.1152/ajprenal.1996.270.5.F812
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Previous investigations have demonstrated that growing mesangial cells in high glucose concentration stimulates extracellular matrix synthesis and also increases the expression of transforming growth factor-beta (TGF-beta). We examined the effects of hyperglycemia on mesangial proliferation and heparan sulfate proteoglycan (HSPG) and fibronectin production. Prolonged exposure of mesangial cells to increasing glucose concentrations resulted in dose-dependent effects on growth inhibition and stimulation of matrix production. Treatment of mesangial cells with high glucose-conditioned medium or with TGF-beta 1 mimicked the effects of high-glucose incubation. Furthermore, TGF-beta 1 caused a dose-dependent increase in HSPG mRNA levels. The high-glucose effects on mesangial cells were preceded by an increase in total TGF-beta 1 protein. The presence of TGF-beta 1 antisense oligonucleotide attenuated the glucose-mediated effects on mesangial proliferation and matrix production. The data show that even moderately elevated glucose concentrations appear to affect the mesangial cells. The results indicate that 1) TGF-beta 1 protein production is necessary to obtain the high glucose-induced effects and 2) TGF-beta 1 stimulates mesangial HSPG expression and production. Because these effects may be attenuated by oligonucleotides antisense to TGF-beta 1, the results suggest a possible way for effective intervention in TGF-beta-mediated glomerulosclerosis.
引用
收藏
页码:F812 / F821
页数:10
相关论文
共 39 条
  • [1] INCREASED EXTRACELLULAR-MATRIX SYNTHESIS AND MESSENGER-RNA IN MESANGIAL CELLS GROWN IN HIGH-GLUCOSE MEDIUM
    AYO, SH
    RADNIK, RA
    GLASS, WF
    GARONI, JA
    RAMPT, ER
    APPLING, DR
    KREISBERG, JI
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (02): : F185 - F191
  • [2] BASEMENT-MEMBRANE HEPARAN-SULFATE PROTEOGLYCAN BINDS TO LAMININ BY ITS HEPARAN-SULFATE CHAINS AND TO NIDOGEN BY SITES IN THE PROTEIN CORE
    BATTAGLIA, C
    MAYER, U
    AUMAILLEY, M
    TIMPL, R
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 208 (02): : 359 - 366
  • [3] TGF-BETA INDUCES BIMODAL PROLIFERATION OF CONNECTIVE-TISSUE CELLS VIA COMPLEX CONTROL OF AN AUTOCRINE PDGF LOOP
    BATTEGAY, EJ
    RAINES, EW
    SEIFERT, RA
    BOWENPOPE, DF
    ROSS, R
    [J]. CELL, 1990, 63 (03) : 515 - 524
  • [4] TRANSFORMING GROWTH FACTOR-B REGULATES PRODUCTION OF PROTEOGLYCANS BY MESANGIAL CELLS
    BORDER, WA
    OKUDA, S
    LANGUINO, LR
    RUOSLAHTI, E
    [J]. KIDNEY INTERNATIONAL, 1990, 37 (02) : 689 - 695
  • [5] INACTIVATION OF THE TYPE-II RECEPTOR REVEALS 2 RECEPTOR PATHWAYS FOR THE DIVERSE TGF-BETA ACTIVITIES
    CHEN, RH
    EBNER, R
    DERYNCK, R
    [J]. SCIENCE, 1993, 260 (5112) : 1335 - 1338
  • [6] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [7] COIMBRA T, 1991, AM J PATHOL, V138, P223
  • [8] MODES OF FGF RELEASE INVIVO AND INVITRO
    DAMORE, PA
    [J]. CANCER AND METASTASIS REVIEWS, 1990, 9 (03) : 227 - 238
  • [9] IMPROVED SANDWICH ENZYME-LINKED IMMUNOSORBENT ASSAYS FOR TRANSFORMING GROWTH FACTOR-BETA-1
    DANIELPOUR, D
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 158 (01) : 17 - 25
  • [10] DOI T, 1992, P NATL ACAD SCI USA, V89, P2873, DOI 10.1073/pnas.89.7.2873