Functional MR Microimaging of Pancreatic β-Cell Activation

Author:

Gimi Barjor12,Leoni Lara234,Oberholzer Jose25,Braun Mark5,Avila Jose5,Wang Yong5,Desai Tejal6,Philipson Louis H.7,Magin Richard L.2,Roman Brian B.234

Affiliation:

1. Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, 720 Rutland Avenue, Baltimore, MD, 21205, USA

2. Department of Bioengineering, University of Illinois at Chicago, 851 S. Morgan St., Chicago, IL, 60607, USA

3. Department of Physiology and Biophysics, Center for Cardiovascular Research, University of Illinois at Chicago, 840 S. Wood St., Chicago, IL, 60612, USA

4. Department of Radiology, University of Chicago, 5841 South Maryland Ave, Chicago, IL, 60637, USA

5. Division of Transplantation, Hospital, University of Illinois at Chicago, 840 S. Wood St., Chicago, IL, 60612, USA

6. Department of Biomedical Engineering, Boston University, 44 Cummington St., Boston, MA, 20215, USA

7. Department of Medicine, Section of Endocrinology, University of Chicago, 5841 South Maryland Ave, Chicago, IL, 60637, USA

Abstract

The increasing incidence of diabetes and the need to further understand its cellular basis has resulted in the development of new diagnostic and therapeutic techniques. Nonetheless, the quest to noninvasively ascertain β-cell mass and function has not been achieved. Manganese (Mn)-enhanced MRI is presented here as a tool to image β-cell functionality in cell culture and isolated islets. Similar to calcium, extracellular Mn was taken up by glucose-activated β-cells resulting in 200% increase in MRI contrast enhancement, versus nonactivated cells. Similarly, glucose-activated islets showed an increase in MRI contrast up to 45%. Although glucose-stimulated Ca influx was depressed in the presence of 100 μM Mn, no significant effect was seen at lower Mn concentrations. Moreover, islets exposed to Mn showed normal glucose sensitivity and insulin secretion. These results demonstrate a link between image contrast enhancement and β-cell activation in vitro, and provide the basis for future noninvasive in vivo imaging of islet functionality and β-cell mass.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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