APOPTOSIS IN THE RAT CORNEAL EPITHELIUM DURING REGENERATION - A TRANSMISSION ELECTRON-MICROSCOPIC STUDY

被引:13
作者
GLASO, M
SANDVIG, KU
HAASKJOLD, E
机构
[1] UNIV OSLO,NATL HOSP,INST PATHOL,ELECTRON MICROSCOP LAB,OSLO,NORWAY
[2] UNIV OSLO,NATL HOSP,CELL KINET LAB,OSLO,NORWAY
[3] UNIV OSLO,NATL HOSP,DEPT OPHTHALMOL,OSLO,NORWAY
[4] UNIV OSLO,NATL HOSP,DEPT EXPTL ANIM,OSLO,NORWAY
关键词
APOPTOSIS; CELL DEATH; CORNEA; EPITHELIUM; HOMEOSTASIS; WOUND HEALING; ELECTRON MICROSCOPY;
D O I
10.1111/j.1699-0463.1993.tb00201.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the present transmission electron microscopic study, regenerating rat corneal epithelium is examined at three different time points after chemical abrasion. Four days after the initial injury classical signs of regeneration are observed. At day 6 regeneration is less pronounced and epithelial differentiation dominates the morphological picture. Many basal cells are swollen and single electron-dense basal cells have a shrunken morphology (dark cells). Intercellular cytoplasmic sacs are common and some appear to be phagocytosed. At day 8 there are no signs of regeneration and neither dark cells nor swollen cytoplasmic sacs are seen. No signs of intraepithelial inflammation are seen at any time. ''Odland''-like granules, which possibly play a role in epithelial desquamation, occur suprabasally in large numbers at all time points. We believe the simultaneous presence of dark cells and phagocytosis at day 6, without signs of inflammation, indicates ongoing apoptosis. Intraepithelial cell loss might explain the discrepancy between an increased proliferation rate and the absence of hyperplasia which has been reported at this time point.
引用
收藏
页码:914 / 922
页数:9
相关论文
共 20 条
[1]  
AITKEN D, 1988, INVEST OPHTH VIS SCI, V29, P224
[2]  
BJERKNES R, 1977, THESIS U I PATHOLOGY, P17
[3]  
BUDTZ P, 1991, THESIS COPENHAGEN
[4]   DETERMINATION OF THE LENGTH OF THE HISTOLOGICAL STAGES OF APOPTOSIS IN NORMAL LIVER AND IN ALTERED HEPATIC FOCI OF RATS [J].
BURSCH, W ;
PAFFE, S ;
PUTZ, B ;
BARTHEL, G ;
SCHULTEHERMANN, R .
CARCINOGENESIS, 1990, 11 (05) :847-853
[5]  
GHADIALLY FN, 1985, DIAGNOSTIC ELECTRON, P326
[6]   THE INFLUENCE OF FIXATION ON THE MORPHOLOGY OF MOUSE EPIDERMIS - A LIGHT AND ELECTRON-MICROSCOPIC STUDY WITH SPECIAL REFERENCE TO DARK CELLS AND EPIDERMAL CARCINOGENESIS [J].
GLASO, M ;
HOVIG, T .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1987, 54 (02) :73-88
[7]  
GLASO M, 1991, THESIS U OSLO NORWAY
[8]  
GLAUERT AM, 1974, PRACTICAL METHODS EL, V3, P5
[9]  
HAASKJOLD E, 1989, ACTA OPHTHALMOL, V67, P174
[10]  
HARMON BV, 1987, J PATHOL, V153, P354