Modelling the effects of vascular stress in mesangial cells

被引:44
作者
Riser, BL [1 ]
Cortes, P [1 ]
Yee, J [1 ]
机构
[1] Henry Ford Hosp, Dept Internal Med, Div Nephrol, Detroit, MI 48202 USA
关键词
D O I
10.1097/00041552-200001000-00008
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
It has recently been shown that mesangial cells are subjected to multiple forms of mechanical strain (fluid shear, hydrostatic pressure, and triaxial stretch) as a result of forces exerted by the vasculature. Nevertheless, the exact nature and the relative response to these stimuli have not been clarified. Although it is now well established that cyclic stretching of mesangial cells in culture results in the overproduction of extracellular matrix, indicating how intraglomerular hypertension may lead to glomerular scar formation, the contribution of different intracellular signalling mechanisms and extracellular mediators of the response are only now being identified, Recent studies point to a role for high glucose concentrations, transforming growth factor beta and its receptors, vascular endothelial growth factor, and connective tissue growth factor as important mediators, or modifiers of the response to mechanical strain. Although evidence exists for a role for protein kinase C, recent studies also implicate the mitogen-activated protein kinases along with enhanced DNA-binding activity of AP-1 as part of the signalling cascade altering matrix synthesis and cell proliferation in response to stretch, Finally, recent studies examining the effects of oscillating hyperbaric pressure demonstrate similarities, as well as differences, in comparison to those of cyclic stretch, Cun Opin Nephrol Hypertens 9:43-47, (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:43 / 47
页数:5
相关论文
共 36 条
[1]   MECHANICAL STRETCH/RELAXATION OF CULTURED RAT MESANGIAL CELLS INDUCES PROTOONCOGENES AND CYCLOOXYGENASE [J].
AKAI, Y ;
HOMMA, T ;
BURNS, KD ;
YASUDA, T ;
BADR, KF ;
HARRIS, RC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02) :C482-C490
[2]   CONTROL OF GLOMERULAR HYPERTENSION LIMITS GLOMERULAR INJURY IN RATS WITH REDUCED RENAL MASS [J].
ANDERSON, S ;
MEYER, TW ;
RENNKE, HG ;
BRENNER, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (02) :612-619
[3]  
Ando Joji, 1993, Frontiers of Medical and Biological Engineering, V5, P245
[4]   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
[5]   DYNAMICS OF GLOMERULAR ULTRAFILTRATION IN RAT [J].
BRENNER, BM ;
TROY, JL ;
DAUGHARTY, TM .
JOURNAL OF CLINICAL INVESTIGATION, 1971, 50 (08) :1776-+
[6]   Regulation of glomerular volume in normal and partially nephrectomized rats [J].
Cortes, P ;
Zhao, XY ;
Riser, BL ;
Narins, RG .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 270 (02) :F356-F370
[7]  
Cortes P., 1999, Journal of the American Society of Nephrology, V10, p569A
[8]   PROTEINASES AND GLOMERULAR MATRIX TURNOVER [J].
DAVIES, M ;
MARTIN, J ;
THOMAS, GJ ;
LOVETT, DH .
KIDNEY INTERNATIONAL, 1992, 41 (03) :671-678
[9]  
Elger M, 1998, Adv Anat Embryol Cell Biol, V139, P1
[10]  
Grotendorst GR, 1996, CELL GROWTH DIFFER, V7, P469