Diabetes mellitus is characterized by the selective destruction of insulin-producing beta-cells, which leads to a deficiency in insulin secretion and as a result, to hyperglycemia. A promising treatment for type I diabetes is pancreatic islet transplantation which is currently in clinical trials. It is clear now that in order to follow the fate of transplanted islets, reliable non-invasive methods are required. Unfortunately, such non-invasive techniques are currently not available. However, if developed, these methods would provide spatial and temporal information regarding location, function and viability of transplanted islets. Continuing development of molecular imaging probes and non-invasive imaging methods could be successfully applied to labeling and imaging of transplanted pancreatic islets. This would allow evaluating the outcome of human islet transplantation in animal models and ultimately in a clinical setting. Based on our prior experience in imaging autoimmune attack in pancreatic islets using crosslinked superparamagnetic iron oxide nanoparticles (CLIO) and their derivatives (1; 2), we propose to utilize these compounds for labeling human pancreatic islets with subsequent detection by magnetic resonance imaging (MRJ) upon islet transplantation. Furthermore, by conjugating CLIO with a near-infrared probe (Cy5.5 dye), we will be able to confirm MR imaging results using another non-invasive modality - near-infrared optical imaging (NIRF). Multi-modal imaging probes that combine the advantages of both methods have been successfully used in our laboratory (3). Therefore, the overall goal of this application is two-fold. First, we seek to determine the feasibility of labeling human pancreatic islets with a multi-modal imaging probe (CLIO-Cy5.5). We will also study islet function and viability upon labeling. Second, we will investigate if labeled islets can be visualized non-invasively after their transplantation using high-resolution magnetic resonance imaging (MRI) and near-infrared optical imaging in an animal model of diabetes. If successful, this research can be further translated into human studies as similar imaging probes are already in clinical trials (4).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DK071225-01
Application #
6928825
Study Section
Special Emphasis Panel (ZDK1-GRB-3 (J1))
Program Officer
Laughlin, Maren R
Project Start
2005-04-01
Project End
2007-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
1
Fiscal Year
2005
Total Cost
$387,000
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Moore, Anna (2009) Advances in beta-cell imaging. Eur J Radiol 70:254-7
Evgenov, Natalia V; Pratt, John; Pantazopoulos, Pamela et al. (2008) Effects of glucose toxicity and islet purity on in vivo magnetic resonance imaging of transplanted pancreatic islets. Transplantation 85:1091-8
Hillman, Elizabeth M C; Moore, Anna (2007) All-optical anatomical co-registration for molecular imaging of small animals using dynamic contrast. Nat Photonics 1:526-530
Medarova, Zdravka; Evgenov, Natalia V; Dai, Guangping et al. (2006) In vivo multimodal imaging of transplanted pancreatic islets. Nat Protoc 1:429-35
Evgenov, Natalia V; Medarova, Zdravka; Dai, Guangping et al. (2006) In vivo imaging of islet transplantation. Nat Med 12:144-8
Evgenov, Natalia V; Medarova, Zdravka; Pratt, John et al. (2006) In vivo imaging of immune rejection in transplanted pancreatic islets. Diabetes 55:2419-28