A Zebrafish Model of Diabetes Mellitus and Metabolic Memory

被引:68
作者
Intine, Robert V. [1 ]
Olsen, Ansgar S. [1 ]
Sarras, Michael P. [2 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Dr William M Scholl Coll Podiatr Med, N Chicago, IL USA
[2] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, N Chicago, IL USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2013年 / 72期
基金
美国国家卫生研究院;
关键词
Medicine; Issue; 72; Genetics; Genomics; Physiology; Anatomy; Biomedical Engineering; Metabolomics; Zebrafish; diabetes; metabolic memory; tissue regeneration; streptozocin; epigenetics; Danio rerio; animal model; diabetes mellitus; drug discovery; hyperglycemia; TRANSGENERATIONAL EPIGENETIC INHERITANCE; GLYCEMIC CONTROL; GLUCOSE CONTROL; DISEASE; ACCORD; COMPLICATIONS; RETINOPATHY; MECHANISMS; STRESS; HEALTH;
D O I
10.3791/50232
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Diabetes mellitus currently affects 346 million individuals and this is projected to increase to 400 million by 2030. Evidence from both the laboratory and large scale clinical trials has revealed that diabetic complications progress unimpeded via the phenomenon of metabolic memory even when glycemic control is pharmaceutically achieved. Gene expression can be stably altered through epigenetic changes which not only allow cells and organisms to quickly respond to changing environmental stimuli but also confer the ability of the cell to "memorize" these encounters once the stimulus is removed. As such, the roles that these mechanisms play in the metabolic memory phenomenon are currently being examined. We have recently reported the development of a zebrafish model of type I diabetes mellitus and characterized this model to show that diabetic zebrafish not only display the known secondary complications including the changes associated with diabetic retinopathy, diabetic nephropathy and impaired wound healing but also exhibit impaired caudal fin regeneration. This model is unique in that the zebrafish is capable to regenerate its damaged pancreas and restore a euglycemic state similar to what would be expected in post-transplant human patients. Moreover, multiple rounds of caudal fin amputation allow for the separation and study of pure epigenetic effects in an in vivo system without potential complicating factors from the previous diabetic state. Although euglycemia is achieved following pancreatic regeneration, the diabetic secondary complication of fin regeneration and skin wound healing persists indefinitely. In the case of impaired fin regeneration, this pathology is retained even after multiple rounds of fin regeneration in the daughter fin tissues. These observations point to an underlying epigenetic process existing in the metabolic memory state. Here we present the methods needed to successfully generate the diabetic and metabolic memory groups of fish and discuss the advantages of this model.
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页数:7
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