Imaging β-cell death with a near-infrared probe

被引:29
作者
Medarova, Z
Bonner-Weir, S
Lipes, M
Moore, A
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp,MIT, Dept Radiol,Athinoula A Martinos Ctr Biomed Imagi, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Joslin Diabet Ctr, Boston, MA 02115 USA
关键词
D O I
10.2337/diabetes.54.6.1780
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Evidence exists for an essential role of beta-cell apoptosis in the pathology of type 1 and type 2 diabetes. Current methods for diabetes-associated apoptosis detection, however, suffer the drawbacks of relying on in situ-based strategies. In this study, we attempted to measure, both in vitro and ex vivo, levels of beta-cell apoptosis in diabetic mice using Cy5.5-labeled annexin V. We used streptozotocin-treated BALB/c mice and NOD mice of different ages as models of type 1 diabetes and db/db mice as a model of type 2 diabetes. With annexin V Cy5.5, we established differences in levels of apoptosis between diabetic and control animals. Intravenously administered annexin V Cy5.5 accumulated in pancreata of diabetic mice but not in nondiabetic controls. Furthermore, its localization was specific to apoptotic events within diabetic islets; its selectivity was supported by transferase-mediated dUTP nick-end labeling staining. Because annexin V defines an early marker of apoptosis and the developed probe is suitable for in vivo administration, it may provide a promising tool for real-time identification in intact animals of the earliest stages of diabetes-associated beta-cell death and for tracing the events that characterize the pathology of the disease.
引用
收藏
页码:1780 / 1788
页数:9
相关论文
共 70 条
[1]   Irreversibility of nutritionally induced NIDDM in Psammomys obesus is related to β-cell apoptosis [J].
Bar-On, H ;
Ben-Sasson, R ;
Ziv, E ;
Arar, N ;
Shafrir, E .
PANCREAS, 1999, 18 (03) :259-265
[2]  
Bellone M, 1997, J IMMUNOL, V159, P5391
[3]   β-cell death and mass in syngeneically transplanted islets exposed to short- and long-term hyperglycemia [J].
Biarnés, M ;
Montolio, M ;
Nacher, V ;
Raurell, M ;
Soler, J ;
Montanya, E .
DIABETES, 2002, 51 (01) :66-72
[4]   In vivo detection and imaging of phosphatidylserine expression during programmed cell death [J].
Blankenberg, FG ;
Katsikis, PD ;
Tait, JF ;
Davis, RE ;
Naumovski, L ;
Ohtsuki, K ;
Kopiwoda, S ;
Abrams, MJ ;
Darkes, M ;
Robbins, RC ;
Maecker, HT ;
Strauss, HW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6349-6354
[5]   Comparison between human pharmacokinetics and imaging properties of two conjugation methods for 99mTc-Annexin A5 [J].
Boersma, HH ;
Liem, IH ;
Kemerink, GJ ;
Thimister, PWL ;
Hofstra, L ;
Stolk, LML ;
van Heerde, WL ;
Pakbiers, MTW ;
Janssen, D ;
Beysens, AJ ;
Reutelingsperger, CPM ;
Heidendal, GAK .
BRITISH JOURNAL OF RADIOLOGY, 2003, 76 (908) :553-560
[6]   β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes [J].
Butler, AE ;
Janson, J ;
Bonner-Weir, S ;
Ritzel, R ;
Rizza, RA ;
Butler, PC .
DIABETES, 2003, 52 (01) :102-110
[7]   Increased susceptibility to streptozotocin-induced β-cell apoptosis and delayed autoimmune diabetes in alkylpurine-DNA-N-glycosylase-deficient mice [J].
Cardinal, JW ;
Margison, GP ;
Mynett, KJ ;
Yates, AP ;
Cameron, DP ;
Elder, RH .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (16) :5605-5613
[8]   The role of Fas in autoimmune diabetes [J].
Chervonsky, AV ;
Wang, Y ;
Wong, FS ;
Visintin, I ;
Flavell, RA ;
Janeway, CA ;
Matis, LA .
CELL, 1997, 89 (01) :17-24
[9]   Vulnerability of islets in the immediate posttransplantation period - Dynamic changes in structure and function [J].
Davalli, AM ;
Scaglia, L ;
Zangen, DH ;
Hollister, J ;
BonnerWeir, S ;
Weir, GC .
DIABETES, 1996, 45 (09) :1161-1167
[10]   Hyperglycemia-induced β-cell apoptosis in pancreatic islets of Psammomys obesus during development of diabetes [J].
Donath, MY ;
Gross, DJ ;
Cerasi, E ;
Kaiser, N .
DIABETES, 1999, 48 (04) :738-744