Limb regeneration is impaired in an adult zebrafish model of diabetes mellitus

被引:117
作者
Olsen, Ansgar S. [1 ,2 ]
Sarras, Michael P., Jr. [2 ]
Intine, Robert V. [1 ,2 ]
机构
[1] Rosalind Franklin Univ, Dr William M Scholl Coll Podiatr Med, N Chicago, IL 60064 USA
[2] Rosalind Franklin Univ, Dept Cell Biol & Anat, N Chicago, IL 60064 USA
关键词
TRANSGENIC ZEBRAFISH; ANIMAL-MODELS; PANCREAS; DEGENERATION; DISEASE; GENES;
D O I
10.1111/j.1524-475X.2010.00613.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The zebrafish (Danio rerio) is an established model organism for the study of developmental processes, human disease, and tissue regeneration. We report that limb regeneration is severely impaired in our newly developed adult zebrafish model of type I diabetes mellitus. Intraperitoneal streptozocin injection of adult, wild-type zebrafish results in a sustained hyperglycemic state as determined by elevated fasting blood glucose values and increased glycation of serum protein. Serum insulin levels are also decreased and pancreas immunohistochemisty revealed a decreased amount of insulin signal in hyperglycemic fish. Additionally, the diabetic complications of retinal thinning and glomerular basement membrane thickening (early signs of retinopathy and nephropathy) resulting from the hyperglycemic state were evident in streptozocin-injected fish at 3 weeks. Most significantly, limb regeneration, following caudal fin amputation, is severely impaired in diabetic zebrafish and nonspecific toxic effects outside the pancreas were not found to contribute to impaired limb regeneration. This experimental system using adult zebrafish facilitates a broad spectrum of genetic and molecular approaches to study regeneration in the diabetic background.
引用
收藏
页码:532 / 542
页数:11
相关论文
共 40 条
[1]   Topical instillation of ciliary neurotrophic factor inhibits retinal degeneration in streptozotocin-induced diabetic rats [J].
Aizu, Y ;
Katayama, H ;
Takahama, S ;
Hu, JG ;
Nakagawa, H ;
Oyanagi, K .
NEUROREPORT, 2003, 14 (16) :2067-2071
[2]   Degeneration of retinal neuronal processes and pigment epithelium in the early stage of the streptozotocin-diabetic rats [J].
Aizu, Y ;
Oyanagi, K ;
Hu, JG ;
Nakagawa, H .
NEUROPATHOLOGY, 2002, 22 (03) :161-170
[3]   Old questions, new tools, and some answers to the mystery of fin regeneration [J].
Akimenko, MA ;
Marí-Beffa, M ;
Becerra, J ;
Géraudie, J .
DEVELOPMENTAL DYNAMICS, 2003, 226 (02) :190-201
[4]   Predominant cone photoreceptor dysfunction in a hyperglycaemic model of non-proliferative diabetic retinopathy [J].
Alvarez, Yolanda ;
Chen, Kenneth ;
Reynolds, Alison L. ;
Waghorne, Nora ;
O'Connor, John J. ;
Kennedy, Breandan N. .
DISEASE MODELS & MECHANISMS, 2010, 3 (3-4) :236-245
[5]   Mutagenesis strategies in zebrafish for identifying genes involved in development and disease [J].
Amsterdam, Adam ;
Hopkins, Nancy .
TRENDS IN GENETICS, 2006, 22 (09) :473-478
[6]  
ARMBRUSTER DA, 1987, CLIN CHEM, V33, P2153
[7]   Identification of a zebrafish model of muscular dystrophy [J].
Bassett, D ;
Currie, PD .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2004, 31 (08) :537-540
[8]   Making waves in cancer research: new models in the zebrafish [J].
Berghmans, S ;
Jette, C ;
Langenau, D ;
Hsu, K ;
Stewart, R ;
Look, T ;
Kanki, JP .
BIOTECHNIQUES, 2005, 39 (02) :227-237
[9]   Examining diabetic nephropathy through the lens of mouse genetics [J].
Breyer M.D. ;
Tchekneva E. ;
Qi Z. ;
Takahashi T. ;
Fogo A.B. ;
Harris R.C. .
Current Diabetes Reports, 2007, 7 (6) :459-466
[10]   The "Metabolic Memory": Is More Than Just Tight Glucose Control Necessary to Prevent Diabetic Complications? [J].
Ceriello, Antonio ;
Ihnat, Michael A. ;
Thorpe, Jessica E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (02) :410-415