The transforming growth factor beta system in kidney disease and repair: recent progress and future directions

被引:132
作者
Basile, DP [1 ]
机构
[1] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
关键词
D O I
10.1097/00041552-199901000-00005
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 [临床医学]; 100201 [内科学];
摘要
Transforming growth factor beta is a multifunctional polypeptide growth factor implicated in a variety of renal diseases. The expression of transforming growth factor beta is enhanced in renal diseases and available evidence suggests that its activity in promoting the synthesis of extracellular matrix plays a crucial role in fibrotic deposition and the decline in renal function. Transforming growth factor beta is, however, also expressed in response to renal injury and may play an important role in normal repair processes. It appears that renal diseases may result from the inappropriate regulation of transforming growth factor beta expression. The determination of the factors that mediate transforming growth factor beta activity will be of primary importance in elucidating the mechanisms leading to renal disease or repair after injury. Both in-vitro and in-vivo studies have demonstrated that proteolytic activity, thrombospondin-l, elevated glucose, angiotensin II, oxidant stress and hemodynamic forces regulate transforming growth factor beta activity through both transcriptional and post-transcriptional mechanisms. In some cases, therapies that may partly disrupt renal transforming growth factor beta activity have shown promise in slowing the progression to end-stage renal disease. Curr Opin Nephrol Hypertens 8:21-30. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:21 / 30
页数:10
相关论文
共 134 条
[1]
Induction of apoptosis by DPC4, a transcriptional factor regulated by transforming growth factor-beta through stress-activated protein kinase c-Jun N-terminal kinase (SAPK/JNK) signaling pathway [J].
Atfi, A ;
Buisine, M ;
Mazars, A ;
Gespach, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (40) :24731-24734
[2]
Increased transforming growth factor-beta 1 expression in regenerating rat renal tubules following ischemic injury [J].
Basile, DP ;
Rovak, JM ;
Martin, DR ;
Hammerman, MR .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 270 (03) :F500-F509
[3]
Expression of bcl-2 and bax in regenerating rat renal tubules following ischemic injury [J].
Basile, DP ;
Liapis, H ;
Hammerman, MR .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 272 (05) :F640-F647
[4]
Renal TGF-beta in HIV-associated kidney diseases [J].
Bodi, I ;
Kimmel, PL ;
Abraham, AA ;
Svetkey, LP ;
Klotman, PE ;
Kopp, JB .
KIDNEY INTERNATIONAL, 1997, 51 (05) :1568-1577
[5]
MECHANISMS OF ISCHEMIC ACUTE-RENAL-FAILURE [J].
BONVENTRE, JV .
KIDNEY INTERNATIONAL, 1993, 43 (05) :1160-1178
[6]
SUPPRESSION OF EXPERIMENTAL GLOMERULONEPHRITIS BY ANTISERUM AGAINST TRANSFORMING GROWTH FACTOR-BETA-1 [J].
BORDER, WA ;
OKUDA, S ;
LANGUINO, LR ;
SPORN, MB ;
RUOSLAHTI, E .
NATURE, 1990, 346 (6282) :371-374
[7]
NATURAL INHIBITOR OF TRANSFORMING GROWTH-FACTOR-BETA PROTECTS AGAINST SCARRING IN EXPERIMENTAL KIDNEY-DISEASE [J].
BORDER, WA ;
NOBLE, NA ;
YAMAMOTO, T ;
HARPER, JR ;
YAMAGUCHI, Y ;
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1992, 360 (6402) :361-364
[8]
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[9]
Tissue specific regulation of transforming growth factor beta by omega-3 lipid-rich krill oil in autoimmune murine lupus [J].
Chandrasekar, B ;
Troyer, DA ;
Venkatraman, JT ;
Fernandes, G .
NUTRITION RESEARCH, 1996, 16 (03) :489-503
[10]
BIOCHEMICAL-EVIDENCE FOR THE AUTOPHOSPHORYLATION AND TRANSPHOSPHORYLATION OF TRANSFORMING GROWTH-FACTOR-BETA RECEPTOR KINASES [J].
CHEN, F ;
WEINBERG, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (05) :1565-1569