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首页> 外文期刊>Anatomy and embryology >Apoptosis and occurrence of Bcl-2, Bak, Bax, Fas and FasL in the developing and adult rat endocrine pancreas.
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Apoptosis and occurrence of Bcl-2, Bak, Bax, Fas and FasL in the developing and adult rat endocrine pancreas.

机译:Bcl-2,Bak,Bax,Fas和FasL在发育中和成年大鼠内分泌胰腺中的凋亡和发生。

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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 18 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.
机译:据认为凋亡细胞死亡在胰岛素依赖性和非胰岛素依赖性糖尿病的表现中起关键作用。因此,在大鼠内分泌胰腺中研究了细胞凋亡和凋亡标记物,以了解Langerhans胰岛的可能生命周期。在E19天至18个月之间的13个时间点对胰岛进行了研究。在每个时间点,用直接荧光素标记的TUNEL方法对组织切片进行处理,并对胰激素(胰高血糖素,胰岛素),凋亡促进剂(Bak,Bax,Fas,Fas Ligand)以及抗凋亡肽Bcl进行免疫染色。 -2。使用共聚焦激光扫描显微镜在相同设置下对所有组织切片进行研究,以半定量估算染色强度。 TUNEL阳性细胞发生在出生前或出生后的所有阶段。研究结果表明,大鼠一生中内分泌胰腺具有双相凋亡活性。第一阶段始于E19,在P5达到峰值,伴随Bak荧光染色强度的显着增加,而第二阶段始于P30,在18个月达到峰值,随着胰岛细胞Fas和FasL染色强度的增加。呈现的原位数据对于理解胰岛细胞与年龄相关的脆弱性增加以及对分离和培养的大鼠胰岛的研究可能是重要的。

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