Abstract

BackgroundKidney transplantation (ktx) in mice is used to learn about rejection and to develop new treatment strategies. Past studies have mainly been based on histological or molecular biological methods. Imaging techniques to monitor allograft pathology have rarely been used.MethodsHere we investigated mice after isogenic and allogenic ktx over time with functional MRI with diffusion-weighted imaging (DWI) and mapping of T2-relaxation time (T2-mapping) to assess graft inflammation and edema formation. To characterize graft pathology, we used PAS-staining, counted CD3-positive T-lymphocytes, analyzed leukocytes by means flow cytometry.ResultsDWI revealed progressive restriction of diffusion of water molecules in allogenic kidney grafts. This was paralleled by enhanced infiltration of the kidney by inflammatory cells. Changes in tissue diffusion were not seen following isogenic ktx. T2-times in renal cortex were increased after both isogenic and allogenic transplantation, consistent with tissue edema due to ischemic injury following prolonged cold ischemia time of 60 minutes. Lack of T2 increase in the inner stripe of the inner medulla in allogenic kidney grafts matched loss of tubular autofluorescence and may result from rejection-driven reductions in tubular water content due to tubular dysfunction and renal functional impairment.ConclusionsFunctional MRI is a valuable non-invasive technique for monitoring inflammation, tissue edema and tubular function. It permits on to differentiate between acute rejection and ischemic renal injury in a mouse model of ktx.

Highlights

  • Magnetic resonance imaging (MRI) allows non-invasive and contrast-free longitudinal examination of renal allografts

  • T2-times in renal cortex were increased after both isogenic and allogenic transplantation, consistent with tissue edema due to ischemic injury following prolonged cold ischemia time of 60 minutes

  • It permits on to differentiate between acute rejection and ischemic renal injury in a mouse model of ktx

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Summary

Introduction

Magnetic resonance imaging (MRI) allows non-invasive and contrast-free longitudinal examination of renal allografts. Besides imaging of renal morphology, the standard in the clinics, novel functional MRI (fMRI) techniques allow one to assess the structure and function of the transplant[1,2,3,4,5]. Diagnosis of graft rejection will be important in patients. Mouse models of ktx are frequently used to study mechanisms underlying allograft pathology and to test novel treatment strategies[6, 9]. In these models repetitive fMRI detecting localization and severity of renal inflammation may improve the understanding of disease mechanisms and the effects of therapeutic interventions. Imaging techniques to monitor allograft pathology have rarely been used

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