MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys

Abstract Insulin-producing cells (IPCs) derived from a patient’s own stem cells offer great potential for autologous transplantation in diabetic patients. However, the limited survival of engrafted cells remains a bottleneck in the application of this strategy. The present study aimed to investigate...

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Main Authors: Chunlin Zou, Yi Lu, Xiahong Teng, Shuyan Wang, Xiaoting Sun, Fen Huang, Guannan Shu, Xin Huang, Hongwei Guo, Zhiguo Chen, Jian Zhang, Yu Alex Zhang
Format: Article
Language:English
Published: Nature Portfolio 2017-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-02775-0
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author Chunlin Zou
Yi Lu
Xiahong Teng
Shuyan Wang
Xiaoting Sun
Fen Huang
Guannan Shu
Xin Huang
Hongwei Guo
Zhiguo Chen
Jian Zhang
Yu Alex Zhang
author_facet Chunlin Zou
Yi Lu
Xiahong Teng
Shuyan Wang
Xiaoting Sun
Fen Huang
Guannan Shu
Xin Huang
Hongwei Guo
Zhiguo Chen
Jian Zhang
Yu Alex Zhang
author_sort Chunlin Zou
collection DOAJ
description Abstract Insulin-producing cells (IPCs) derived from a patient’s own stem cells offer great potential for autologous transplantation in diabetic patients. However, the limited survival of engrafted cells remains a bottleneck in the application of this strategy. The present study aimed to investigate whether nanoparticle-based magnetic resonance (MR) tracking can be used to detect the loss of grafted stem cell-derived IPCs in a sensitive and timely manner in a diabetic monkey model. Pancreatic progenitor cells (PPCs) were isolated from diabetic monkeys and labeled with superparamagnetic iron oxide nanoparticles (SPIONs). The SPION-labeled cells presented as hypointense signals on MR imaging (MRI). The labeling procedure did not affect the viability or IPC differentiation of PPCs. Importantly, the total area of the hypointense signal caused by SPION-labeled IPCs on liver MRI decreased before the decline in C-peptide levels after autotransplantation. Histological analysis revealed no detectable immune response to the grafts and many surviving insulin- and Prussian blue-positive cell clusters on liver sections at one year post-transplantation. Collectively, this study demonstrates that SPIO nanoparticles can be used to label stem cells for noninvasive, sensitive, longitudinal monitoring of stem cell-derived IPCs in large animal models using a conventional MR imager.
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spelling doaj.art-c9b45fa05cd54585a97973cc2765bcbb2022-12-21T21:52:22ZengNature PortfolioScientific Reports2045-23222017-05-017111110.1038/s41598-017-02775-0MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeysChunlin Zou0Yi Lu1Xiahong Teng2Shuyan Wang3Xiaoting Sun4Fen Huang5Guannan Shu6Xin Huang7Hongwei Guo8Zhiguo Chen9Jian Zhang10Yu Alex Zhang11Center for Translational Medicine, Guangxi Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCell Therapy Center, Xuanwu Hospital, Capital Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCell Therapy Center, Xuanwu Hospital, Capital Medical UniversityCenter for Translational Medicine, Guangxi Medical UniversityCell Therapy Center, Xuanwu Hospital, Capital Medical UniversityAbstract Insulin-producing cells (IPCs) derived from a patient’s own stem cells offer great potential for autologous transplantation in diabetic patients. However, the limited survival of engrafted cells remains a bottleneck in the application of this strategy. The present study aimed to investigate whether nanoparticle-based magnetic resonance (MR) tracking can be used to detect the loss of grafted stem cell-derived IPCs in a sensitive and timely manner in a diabetic monkey model. Pancreatic progenitor cells (PPCs) were isolated from diabetic monkeys and labeled with superparamagnetic iron oxide nanoparticles (SPIONs). The SPION-labeled cells presented as hypointense signals on MR imaging (MRI). The labeling procedure did not affect the viability or IPC differentiation of PPCs. Importantly, the total area of the hypointense signal caused by SPION-labeled IPCs on liver MRI decreased before the decline in C-peptide levels after autotransplantation. Histological analysis revealed no detectable immune response to the grafts and many surviving insulin- and Prussian blue-positive cell clusters on liver sections at one year post-transplantation. Collectively, this study demonstrates that SPIO nanoparticles can be used to label stem cells for noninvasive, sensitive, longitudinal monitoring of stem cell-derived IPCs in large animal models using a conventional MR imager.https://doi.org/10.1038/s41598-017-02775-0
spellingShingle Chunlin Zou
Yi Lu
Xiahong Teng
Shuyan Wang
Xiaoting Sun
Fen Huang
Guannan Shu
Xin Huang
Hongwei Guo
Zhiguo Chen
Jian Zhang
Yu Alex Zhang
MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys
Scientific Reports
title MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys
title_full MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys
title_fullStr MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys
title_full_unstemmed MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys
title_short MRI tracking of autologous pancreatic progenitor-derived insulin-producing cells in monkeys
title_sort mri tracking of autologous pancreatic progenitor derived insulin producing cells in monkeys
url https://doi.org/10.1038/s41598-017-02775-0
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