Apoptosis and occurrence of Bcl-2, Bak, Bax, Fas and FasL in the developing and adult rat endocrine pancreas
- PMID: 11000281
- DOI: 10.1007/s004290000112
Apoptosis and occurrence of Bcl-2, Bak, Bax, Fas and FasL in the developing and adult rat endocrine pancreas
Abstract
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.
Similar articles
-
Apoptosis in cultured rat islets of langerhans and occurrence of Bcl-2, Bak, Bax, Fas and Fas ligand.Cells Tissues Organs. 2001;169(2):113-24. doi: 10.1159/000047869. Cells Tissues Organs. 2001. PMID: 11399851
-
Alveolar epithelial type II cell apoptosis in vivo during resolution of keratinocyte growth factor-induced hyperplasia in the rat.Histochem Cell Biol. 2000 Jul;114(1):49-61. doi: 10.1007/s004180000157. Histochem Cell Biol. 2000. PMID: 10959822
-
Progressive resistance to apoptosis in a cell lineage model of human proliferative breast disease.J Natl Cancer Inst. 2001 May 16;93(10):776-82. doi: 10.1093/jnci/93.10.776. J Natl Cancer Inst. 2001. PMID: 11353788
-
Coexpression of Fas/FasL and Bax on brain and infiltrating T cells in the central nervous system is closely associated with apoptotic cell death during autoimmune encephalomyelitis.J Neuroimmunol. 2000 Jul 1;106(1-2):165-71. doi: 10.1016/s0165-5728(00)00238-1. J Neuroimmunol. 2000. PMID: 10814794
-
Involvement of Bcl-2 family genes and Fas signaling system in primary and secondary male germ cell apoptosis induced by 2-bromopropane in rat.Toxicol Appl Pharmacol. 2001 Jul 1;174(1):35-48. doi: 10.1006/taap.2001.9187. Toxicol Appl Pharmacol. 2001. PMID: 11437647
Cited by
-
Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines.Biol Proced Online. 2005;7:162-71. doi: 10.1251/bpo113. Epub 2005 Nov 7. Biol Proced Online. 2005. PMID: 16281079 Free PMC article.
-
A GIP receptor agonist exhibits beta-cell anti-apoptotic actions in rat models of diabetes resulting in improved beta-cell function and glycemic control.PLoS One. 2010 Mar 9;5(3):e9590. doi: 10.1371/journal.pone.0009590. PLoS One. 2010. PMID: 20231880 Free PMC article.
-
Regional Downregulation of Dopamine Receptor D1 in Bilateral Dorsal Lateral Geniculate Nucleus of Monocular Form-Deprived Amblyopia Models.Front Neurosci. 2022 Jun 8;16:861529. doi: 10.3389/fnins.2022.861529. eCollection 2022. Front Neurosci. 2022. PMID: 35757538 Free PMC article.
-
Bax and Bak expression in cervical smears of women with low-and high-risk HPV types: A study of 120 cases.J Cytol. 2015 Oct-Dec;32(4):223-9. doi: 10.4103/0970-9371.171222. J Cytol. 2015. PMID: 26811568 Free PMC article.
-
Fas and Fas ligand immunolocalization in pancreatic islets of NOD mice during spontaneous and cyclophosphamide-accelerated diabetes.Histochem J. 2002 Jan-Feb;34(1-2):1-12. doi: 10.1023/a:1021321522826. Histochem J. 2002. PMID: 12365794
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Research Materials
Miscellaneous