DEGENERATED INTRAMURAL PERICYTES (GHOST CELLS) IN THE RETINAL CAPILLARIES OF DIABETIC RATS

被引:64
作者
ROBINSON, WG
MCCALEB, ML
FELD, LG
MICHAELIS, OE
LAVER, N
MERCANDETTI, M
机构
[1] WYETH AYERST RES,METAB DISORDERS,PRINCETON,NJ
[2] CHILDRENS HOSP,DIV NEPHROL,BUFFALO,NY 14222
[3] SUNY BUFFALO,SCH MED & BIOMED SCI,DEPT OPHTHALMOL,BUFFALO,NY 14260
[4] USDA ARS,BELTSVILLE AGR RES CTR,BELTSVILLE HUMAN NUTR RES CTR,BELTSVILLE,MD 20705
关键词
D O I
10.3109/02713689108996340
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
One of the earliest histopathological signs of diabetic retinopathy is a selective loss of intramural pericytes from retinal capillaries. In the present study, the retinal vessels of rats with streptozotocin-induced diabetes (STZ Wistar) and rats with genetically-induced insulin dependent diabetes mellitus (BB Wistar) and non-insulin dependent diabetes mellitus (SHR/N-corpulent) were examined after 6 to 8 months duration for diabetes-related retinal microangiopathies. The SHR/N-corpulent (cp) rats were fed a 54% sucrose diet, whereas the STZ Wistar and BB Wistar rats were fed laboratory chow for 32 to 36 weeks. In all the diabetic rats, the retinal capillaries in enzyme-digested flat mounts exhibited an increase in periodic-acid-Schiff (PAS) staining and loss of pericytes compared to their respective euglycemic controls. Pericyte "ghosts", like those defined in human diabetes as intramural pockets lacking normal cell contents, were documented by high resolution micrographs in all the diabetic rats. Endothelial cell proliferation, capillary dilation, and varicose loop formation were noted in some of the diabetic rats. Hence, similar capillary lesions were found in very different groups of diabetic rats. The findings suggest that a chronic high tissue concentration of glucose is the underlying factor which triggers pathogenesis in the pericyte. Hyperglycemia-induced activation of endogenous aldose reductase of the polyol pathway is probably the initial insult, but other factors such as advanced glycosylation products may affect the final outcome.
引用
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页码:339 / 350
页数:12
相关论文
共 40 条
[31]   CHARACTERIZATION OF MESSENGER-RNA AND GENES FOR ALDOSE REDUCTASE IN RAT [J].
NISHIMURA, C ;
GRAHAM, C ;
HOHMAN, TC ;
NAGATA, M ;
ROBISON, WG ;
CARPER, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (03) :1051-1059
[32]  
ORLIDGE A, 1988, Investigative Ophthalmology and Visual Science, V29, P109
[33]   DEVELOPMENT OF RETINOPATHY IN SUCROSE-FED AND STREPTOZOTOCIN-DIABETIC RATS [J].
PAPACHRISTODOULOU, D ;
HEATH, H ;
KANG, SS .
DIABETOLOGIA, 1976, 12 (04) :367-374
[34]   DIABETES-RELATED HISTOPATHOLOGIES OF THE RAT RETINA PREVENTED WITH AN ALDOSE REDUCTASE INHIBITOR [J].
ROBISON, WG ;
TILLIS, TN ;
LAVER, N ;
KINOSHITA, JH .
EXPERIMENTAL EYE RESEARCH, 1990, 50 (04) :355-366
[35]  
ROBISON WG, 1989, INVEST OPHTH VIS SCI, V30, P2285
[36]  
ROBISON WG, 1989, INVEST OPHTH VIS SCI, V30, P2293
[37]  
ROSENMANN E, 1975, ISRAEL J MED SCI, V11, P753
[38]   THE BB-RAT - AN AUTHENTIC MODEL OF HUMAN DIABETIC-RETINOPATHY [J].
SIMA, AAF ;
CHAKRABARTI, S ;
GARCIASALINAS, R ;
BASU, PK .
CURRENT EYE RESEARCH, 1985, 4 (10) :1087-1092
[39]   THE BB WISTAR RAT - AN EXPERIMENTAL-MODEL FOR THE STUDY OF DIABETIC-RETINOPATHY [J].
SIMA, AAF ;
GARCIASALINAS, R ;
BASU, PK .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1983, 32 (07) :136-140
[40]   THE PERICYTE - A REVIEW [J].
SIMS, DE .
TISSUE & CELL, 1986, 18 (02) :153-174