Quantitative determination of apoptosis of pancreatic β-cells in a murine model of type 1 diabetes mellitus Journal Article


Authors: Watanabe, A.; Nishijima, K. I.; Zhao, S.; Zhao, Y.; Tanaka, Y.; Takemoto, H.; Strauss, H. W.; Blankenberg, F. G.; Tamaki, N.; Kuge, Y.
Article Title: Quantitative determination of apoptosis of pancreatic β-cells in a murine model of type 1 diabetes mellitus
Abstract: Type 1 diabetes mellitus is characterized by a significant deficit in pancreatic β-cell mass, presumably caused by β-cell apoptosis. We investigated the incidence of β-cell apoptosis in streptozotocin-treated mice and nonobese diabetic (NOD) mice with 99mTc-annexin A5. Methods: Vehicle-treated mice, streptozotocin-treated mice, and NOD mice at the ages of 5, 9, 16, and 20 wk (5-8 mice per group) were injected with 99mTc- annexin A5 and sacrificed 6 h later for autoradiography, and the regional 99mTc-annexin A5 level in the pancreas was evaluated. Pancreatic islets were identified by insulin immunohistochemical staining, and apoptotic cells were determined by terminal deoxynucleotidyl transferase - mediated dUTP nickend labeling (TUNEL) staining. The 99mTc- annexin A5 level in pancreatic islets was expressed as the percentage injected dose per area of pancreatic islets and normalized by animal body weight (%ID × 10 6/mm 2/kg). The level of apoptotic cells in pancreatic islets was expressed as the number of TUNEL-positive cells per area of pancreatic islets (cells/mm 2). Results: The 99mTc-annexin A5 accumulation level was significantly higher (2.5 ± 0.7 vs. 0.7 ± 0.1%ID × 10 6/mm 2/kg, P < 0.05) and the number of TUNEL-positive cells was significantly higher (1,170 ± 535 vs. 5 ± 6 cells/mm 2, P < 0.05) in the pancreatic islets of the streptozotocin-treated mice than in those of the vehicle-treated mice. The 99mTc-annexin A5 accumulation level was significantly higher (1.1 ± 0.4 vs. 0.5 ± 0.1%ID × 10 6/mm 2/kg, P < 0.05) and the number of TUNEL-positive cells was significantly higher (152 ± 82 vs. 4 ± 9 cells/mm 2, P < 0.05) in the pancreatic islets of 16-wk-old NOD mice than in those of 5-wk-old NOD mice. In addition, the level of 99mTc-annexin A5 correlated with the number of TUNEL-positive cells in the pancreatic islets of the streptozotocin-treated mice (r = 0.821, P < 0.001) and NOD mice (r = 0.721, P < 0.001). Conclusion: There is significant islet cell apoptosis with 99mTc- annexin A5 accumulation in the pancreas of both streptozotocin and NOD mice. Copyright © 2012 by the Society of Nuclear Medicine and Molecular Imaging, Inc.
Keywords: immunohistochemistry; controlled study; unclassified drug; histopathology; nonhuman; technetium 99m; animal cell; mouse; animals; mice; animal tissue; apoptosis; animal experiment; animal model; body weight; molecular imaging; feasibility studies; quantitative analysis; radiopharmaceutical agent; cellular distribution; glucose blood level; glucose; blood glucose; disease models, animal; insulin dependent diabetes mellitus; diabetes mellitus, type 1; nick end labeling; pancreas islet beta cell; insulin-secreting cells; autoradiography; cell labeling; organotechnetium compounds; annexin a5; 99mtc-annexin a5; type 1 diabetes mellitus; pancreatic beta cells; technetium annexin 5 tc 99m
Journal Title: Journal of Nuclear Medicine
Volume: 53
Issue: 10
ISSN: 0161-5505
Publisher: Society of Nuclear Medicine  
Date Published: 2012-10-01
Start Page: 1585
End Page: 1591
Language: English
DOI: 10.2967/jnumed.111.102459
PROVIDER: scopus
PUBMED: 22930815
DOI/URL:
Notes: --- - "Export Date: 2 November 2012" - "CODEN: JNMEA" - "Source: Scopus"
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  1. Harry W Strauss
    164 Strauss