Antibody to transforming growth factor-β ameliorates tubular apoptosis in unilateral ureteral obstruction

被引:296
作者
Miyajima, A
Chen, J
Lawrence, C
Ledbetter, S
Soslow, RA
Stern, J
Jha, S
Pigato, J
Lemer, ML
Poppas, DP
Vaughan, ED
Felsen, D
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[2] Childrens Hosp New York, Ctr Pediat Urol, New York, NY USA
[3] Childrens Hosp New York, Lab Minimally Invas Urol Surg, New York, NY USA
[4] Childrens Hosp New York, Dept Urol, New York, NY USA
[5] Childrens Hosp New York, Dept Pathol, New York, NY USA
[6] Genzyme Corp, Framingham, MA 01701 USA
关键词
renal tubular obstruction; cell death; fibrosis; progressive renal atrophy; monoclonal antibody;
D O I
10.1046/j.1523-1755.2000.00414.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Unilateral ureteral obstruction (UUO) is characterized by progressive renal atrophy, renal interstitial fibrosis, an increase in renal transforming growth factor-beta (TGF-beta), and renal tubular apoptosis. The present study was undertaken to determine the effect of a monoclonal antibody to TGF-beta (ID11) in UUO. Methods. Mechanical stretch was applied to tubular epithelial cells (NRK-52E) by a computer-assisted system. Three doses of 1D11 (either 0.5, 2, or 4 mg/rat) were administered to rats one day prior to UUO and every two days thereafter, and kidneys were harvested at day 13. Fibrosis was assessed by measuring tissue hydroxyproline and mRNA for collagen and fibronectin. Apoptosis was assessed with the terminal deoxy transferase uridine triphosphate nick end-labeling assay. TGF-beta levels were determined by bioassay. Western blot and immunostaining were used to identify proliferating cell nuclear antigen (PCNA), p53, bcl-2, and inducible nitric oxide synthase (iNOS). Results. Stretch significantly induced apoptosis in NRK-52E cells, which was accompanied by an increased release of TGF-beta; 1D11 (10 mug/mL) totally inhibited stretch-induced apoptosis. Control obstructed kidney contained 20-fold higher TGF-beta as compared with its unobstructed kidney; 1D11 neutralized tissue TGF-beta of the obstructed kidney. Control obstructed kidney exhibited significantly more fibrosis and tubular apoptosis than its unobstructed counterpart, which was blunted by 1D11. In contrast, 1D11 significantly increased tubular proliferation. p53 immunostaining was localized to renal tubular nuclei of control obstructed kidney and was diminished by 1D11. In contrast, bcl-2 was up-regulated in the 1D11-treated obstructed kidney. Total NOS activity and iNOS activity of the obstructed kidney were increased by 1D11 treatment. Conclusion. The present study strongly suggests that an antibody to TGF-beta is a promising agent to prevent renal tubular fibrosis and apoptosis in UUO.
引用
收藏
页码:2301 / 2313
页数:13
相关论文
共 37 条
  • [1] AN ASSAY FOR TRANSFORMING GROWTH-FACTOR-BETA USING CELLS TRANSFECTED WITH A PLASMINOGEN-ACTIVATOR INHIBITOR-1 PROMOTER LUCIFERASE CONSTRUCT
    ABE, M
    HARPEL, JG
    METZ, CN
    NUNES, I
    LOSKUTOFF, DJ
    RIFKIN, DB
    [J]. ANALYTICAL BIOCHEMISTRY, 1994, 216 (02) : 276 - 284
  • [2] Expression of bcl-2 and bax in regenerating rat renal tubules following ischemic injury
    Basile, DP
    Liapis, H
    Hammerman, MR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 272 (05) : F640 - F647
  • [3] SUPPRESSION OF EXPERIMENTAL GLOMERULONEPHRITIS BY ANTISERUM AGAINST TRANSFORMING GROWTH FACTOR-BETA-1
    BORDER, WA
    OKUDA, S
    LANGUINO, LR
    SPORN, MB
    RUOSLAHTI, E
    [J]. NATURE, 1990, 346 (6282) : 371 - 374
  • [4] Chevalier RL, 1996, J AM SOC NEPHROL, V7, P1098
  • [5] MACROPHAGES, MONOCYTE CHEMOATTRACTANT PEPTIDE-1, AND TGF-BETA-1 IN EXPERIMENTAL HYDRONEPHROSIS
    DIAMOND, JR
    KEESFOLTS, D
    DING, GH
    FRYE, JE
    RESTREPO, NC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06): : F926 - F933
  • [6] Transforming growth factor-beta(1) abrogates Fas-induced growth suppression and apoptosis of murine bone marrow progenitor cells
    Dybedal, I
    Guan, FG
    Borge, OJ
    Veiby, OP
    Ramsfjell, V
    Nagata, S
    Jacobsen, SEW
    [J]. BLOOD, 1997, 90 (09) : 3395 - 3403
  • [7] EDDY AA, 1994, J AM SOC NEPHROL, V5, P1273
  • [8] IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION
    GAVRIELI, Y
    SHERMAN, Y
    BENSASSON, SA
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 119 (03) : 493 - 501
  • [9] GLUMOFF V, 1994, BBA-GENE STRUCT EXPR, V1217, P41, DOI 10.1016/0167-4781(94)90122-8
  • [10] GULMI FA, 1998, CAMPBELLS UROLOGY