Effects of mechanical stress and high glucose on pericyte proliferation, apoptosis and contractile phenotype

被引:25
作者
Beltramo, Elena [1 ]
Berrone, Elena [1 ]
Giunti, Sara [1 ]
Gruden, Gabriella [1 ]
Perin, Paolo Cavallo [1 ]
Porta, Massimo [1 ]
机构
[1] Univ Turin, Dept Internal Med, I-10126 Turin, Italy
关键词
pericytes; mechanical stress; high glucose; replication; apoptosis; cytoskeleton; diabetic retinopathy;
D O I
10.1016/j.exer.2006.05.008
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Pericyte loss is an early step of diabetic retinopathy. High glucose induces apoptosis in retinal pericytes, but systemic and capillary hypertension are also believed to be important in the onset and progression of diabetic retinopathy. The haemodynamic insult of retinal capillary hypertension can be mimicked by exposing pericytes to mechanical stretch. We investigated the effect of stretch combined with high glucose on pericyte proliferation/apoptosis and morphology. Bovine retinal pericytes, cultured in either normal or high glucose concentrations in flexible-base plates, were exposed to mechanical stretch for 48/72 h. Cell replication was determined by both cell counting and DNA synthesis, apoptosis by ELISA, cell morphology and actin cytoskeleton distribution by immunofluorescence. Both reduction in cell proliferation and increase in apoptosis were confirmed in high glucose alone. When cells were subjected to stretch, proliferation was reduced and apoptosis increased in both normal and high glucose in comparison with unstretched controls. In both cases, a synergistic effect of hyperglycaemia combined with stretch was shown. Cell morphology showed modifications of cytoskeleton in all experimental conditions; in particular, cells subjected to stretch showed a clear elongation and translocation of actin fibres. In conclusion, our results show that stretch, alone or combined with high glucose, reduces cell proliferation, increases apoptosis and induces morphological changes in pericyte cytoskeleton. Further elucidations of the mechanisms on the basis of reduced proliferation of pericytes subjected to high glucose and stretch could help to clarify the effects of combined hyperglycaemia and hypertension in the pathogenesis of diabetic retinopathy. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:989 / 994
页数:6
相关论文
共 35 条
[1]   Diabetic retinopathy [J].
Aiello, LP ;
Gardner, TW ;
King, GL ;
Blankenship, G ;
Cavallerano, JD ;
Ferris, FL ;
Klein, R .
DIABETES CARE, 1998, 21 (01) :143-156
[2]  
BARNES AJ, 1985, J CELL SCI, V75, P35
[3]   Thiamine and benfotiamine prevent increased apoptosis in endothelial cells and pericytes cultured in high glucose [J].
Beltramo, E ;
Berrone, E ;
Buttiglieri, S ;
Porta, M .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2004, 20 (04) :330-336
[4]   Dehydroepiandrosterone protects bovine retinal capillary pericytes against glucose toxicity [J].
Brignardello, E ;
Beltramo, E ;
Molinatti, PA ;
Aragno, M ;
Gatto, V ;
Tamagno, E ;
Danni, O ;
Porta, M ;
Boccuzzi, G .
JOURNAL OF ENDOCRINOLOGY, 1998, 158 (01) :21-26
[5]   F-actin fiber distribution in glomerular cells:: Structural and functional implications [J].
Cortes, P ;
Méndez, M ;
Riser, BL ;
Guérin, CJ ;
Rodríguez-Barbero, A ;
Hassett, C ;
Yee, J .
KIDNEY INTERNATIONAL, 2000, 58 (06) :2452-2461
[6]   MECHANICAL-STRESS MECHANISMS AND THE CELL - AN ENDOTHELIAL PARADIGM [J].
DAVIES, PF ;
TRIPATHI, SC .
CIRCULATION RESEARCH, 1993, 72 (02) :239-245
[7]  
Dosso AA, 1999, INVEST OPHTH VIS SCI, V40, P2405
[8]   Activation of a local tissue angiotensin system in podocytes by mechanical strain [J].
Durvasula, RV ;
Petermann, AT ;
Hiromura, K ;
Blonski, M ;
Pippin, J ;
Mundel, P ;
Pichler, R ;
Griffin, S ;
Couser, WG ;
Shankland, SJ .
KIDNEY INTERNATIONAL, 2004, 65 (01) :30-39
[9]  
GILLIES MC, 1993, INVEST OPHTH VIS SCI, V34, P3396
[10]   Mechanical stretch-induced fibronectin and transforming growth factor-β1 production in human mesangial cells is p38 mitogen-activated protein kinase-dependent [J].
Gruden, G ;
Zonca, S ;
Hayward, A ;
Thomas, S ;
Maestrini, S ;
Gnudi, L ;
Viberti, G .
DIABETES, 2000, 49 (04) :655-661