Apoptosis and occurrence of Bcl-2, Bak, Bax, Fas and FasL in the developing and adult rat endocrine pancreas

被引:27
作者
Hanke, J [1 ]
机构
[1] Hannover Med Sch, Dept Anat, D-3000 Hannover, Germany
来源
ANATOMY AND EMBRYOLOGY | 2000年 / 202卷 / 04期
关键词
Bcl-2; family; pancreatic islets; confocal laser scanning microscopy; TUNEL; aging;
D O I
10.1007/s004290000112
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Apoptotic cell death is thought to play a crucial role in the manifestation of insulin- and non-insulin dependent diabetes mellitus. Therefore, apoptosis and apoptotic markers were studied in the rat endocrine pancreas to get insight into the possible life cycle of Langerhans islets. The islets were investigated at 13 time points between day E19 and is months. At each time point, histologic sections were treated with the direct fluorescein-labelled TUNEL method and immunostained for pancreatic hormones (glucagon, insulin), apoptotic promoters (Bak, Bax, Fas, Fas Ligand) as well as for the anti-apoptotic peptide Bcl-2. All tissue sections were investigated using confocal laser scanning microscopy under identical settings for semiquantitative estimation of staining intensity. TUNEL-positive cells occurred in all pre- or postnatal stages. The findings indicated a biphasic apoptotic activity in the endocrine pancreas during the lifetime of rats. The first phase began at E19 and peaked at P5 accompanied by a considerable increase in Bak fluorescence staining intensity, while the second phase began at P30 and peaked at 18 months with increasing amounts of Fas and FasL staining intensities in the islet cells. The presented in situ data may be important for understanding the increased age-related vulnerability of islet cells and for studies of isolated and cultivated rat islets.
引用
收藏
页码:303 / 312
页数:10
相关论文
共 37 条
[1]  
Babcock GF, 1999, METHOD ENZYMOL, V307, P319
[2]  
BOGLER O, 1993, HISTOCHEM J, V25, P746
[3]   Islet morphogenesis and stem cell markers in rat pancreas [J].
Bouwens, L ;
DeBlay, E .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1996, 44 (09) :947-951
[4]   THE BCL-2 CANDIDATE PROTO-ONCOGENE PRODUCT IS A 24-KILODALTON INTEGRAL-MEMBRANE PROTEIN HIGHLY EXPRESSED IN LYMPHOID-CELL LINES AND LYMPHOMAS CARRYING THE T(14,18) TRANSLOCATION [J].
CHENLEVY, Z ;
NOURSE, J ;
CLEARY, ML .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (02) :701-710
[6]   Fas-FasL interactions: a common pathogenetic mechanism in organ-specific autoimmunity [J].
De Maria, R ;
Testi, R .
IMMUNOLOGY TODAY, 1998, 19 (03) :121-125
[7]   DYNAMICS OF BETA-CELL MASS IN THE GROWING RAT PANCREAS - ESTIMATION WITH A SIMPLE MATHEMATICAL-MODEL [J].
FINEGOOD, DT ;
SCAGLIA, L ;
BONNERWEIR, S .
DIABETES, 1995, 44 (03) :249-256
[8]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[9]  
GORCZYCA W, 1993, CANCER RES, V53, P1945
[10]   Growth factor protection against cytokine-induced apoptosis in neonatal rat islets of Langerhans: role of Fas [J].
Harrrison, M ;
Dunger, AM ;
Berg, S ;
Mabley, J ;
John, N ;
Green, MHL ;
Green, IC .
FEBS LETTERS, 1998, 435 (2-3) :207-210