Magnetic Resonance Imaging of Transplanted Porcine Neonatal Pancreatic Cell Clusters Labeled with Chitosan-Coated Superparamagnetic Iron Oxide Nanoparticles in Mice
Neonatal pancreatic cell clusters (NPCCs) are potential tissues for the treatment of diabetes. Different from adult cells, they continuously proliferate and differentiate after transplantation. In this study, we utilized magnetic resonance imaging (MRI) to detect and monitor implanted NPCCs. NPCCs w...
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Published in | Polymers Vol. 13; no. 8; p. 1238 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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11.04.2021
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ISSN | 2073-4360 2073-4360 |
DOI | 10.3390/polym13081238 |
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Abstract | Neonatal pancreatic cell clusters (NPCCs) are potential tissues for the treatment of diabetes. Different from adult cells, they continuously proliferate and differentiate after transplantation. In this study, we utilized magnetic resonance imaging (MRI) to detect and monitor implanted NPCCs. NPCCs were isolated from one-day-old neonatal pigs, cultured for three days, and then incubated overnight with the contrast agent chitosan-coated superparamagnetic iron oxide (CSPIO) nanoparticles. In vitro, Prussian blue staining and MR scans of CSPIO-labeled NPCCs were performed. In vivo, we transplanted 2000 CSPIO-labeled NPCCs under the kidney capsule of nondiabetic nude mice. Recipients were scanned with 7.0T MRI. Grafts were removed for histology with insulin and Prussian blue staining. After being incubated overnight with CSPIO, NPCCs showed positive iron staining and appeared as dark spots on MR scans. After transplantation of CSPIO-labeled NPCCs, persistent hypointense areas were observed at recipients’ implant sites for up to 54 days. Moreover, histology showed colocalization of the insulin and iron staining in 15-, 51- and 55-day NPCC grafts. Our results indicate that transplanted NPCCs survived and differentiated to β cells after transplantation, and that MRI is a useful tool for the detection and monitoring of CSPIO-labeled NPCC grafts. |
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AbstractList | Neonatal pancreatic cell clusters (NPCCs) are potential tissues for the treatment of diabetes. Different from adult cells, they continuously proliferate and differentiate after transplantation. In this study, we utilized magnetic resonance imaging (MRI) to detect and monitor implanted NPCCs. NPCCs were isolated from one-day-old neonatal pigs, cultured for three days, and then incubated overnight with the contrast agent chitosan-coated superparamagnetic iron oxide (CSPIO) nanoparticles. In vitro, Prussian blue staining and MR scans of CSPIO-labeled NPCCs were performed. In vivo, we transplanted 2000 CSPIO-labeled NPCCs under the kidney capsule of nondiabetic nude mice. Recipients were scanned with 7.0T MRI. Grafts were removed for histology with insulin and Prussian blue staining. After being incubated overnight with CSPIO, NPCCs showed positive iron staining and appeared as dark spots on MR scans. After transplantation of CSPIO-labeled NPCCs, persistent hypointense areas were observed at recipients' implant sites for up to 54 days. Moreover, histology showed colocalization of the insulin and iron staining in 15-, 51- and 55-day NPCC grafts. Our results indicate that transplanted NPCCs survived and differentiated to β cells after transplantation, and that MRI is a useful tool for the detection and monitoring of CSPIO-labeled NPCC grafts. Neonatal pancreatic cell clusters (NPCCs) are potential tissues for the treatment of diabetes. Different from adult cells, they continuously proliferate and differentiate after transplantation. In this study, we utilized magnetic resonance imaging (MRI) to detect and monitor implanted NPCCs. NPCCs were isolated from one-day-old neonatal pigs, cultured for three days, and then incubated overnight with the contrast agent chitosan-coated superparamagnetic iron oxide (CSPIO) nanoparticles. In vitro, Prussian blue staining and MR scans of CSPIO-labeled NPCCs were performed. In vivo, we transplanted 2000 CSPIO-labeled NPCCs under the kidney capsule of nondiabetic nude mice. Recipients were scanned with 7.0T MRI. Grafts were removed for histology with insulin and Prussian blue staining. After being incubated overnight with CSPIO, NPCCs showed positive iron staining and appeared as dark spots on MR scans. After transplantation of CSPIO-labeled NPCCs, persistent hypointense areas were observed at recipients' implant sites for up to 54 days. Moreover, histology showed colocalization of the insulin and iron staining in 15-, 51- and 55-day NPCC grafts. Our results indicate that transplanted NPCCs survived and differentiated to β cells after transplantation, and that MRI is a useful tool for the detection and monitoring of CSPIO-labeled NPCC grafts.Neonatal pancreatic cell clusters (NPCCs) are potential tissues for the treatment of diabetes. Different from adult cells, they continuously proliferate and differentiate after transplantation. In this study, we utilized magnetic resonance imaging (MRI) to detect and monitor implanted NPCCs. NPCCs were isolated from one-day-old neonatal pigs, cultured for three days, and then incubated overnight with the contrast agent chitosan-coated superparamagnetic iron oxide (CSPIO) nanoparticles. In vitro, Prussian blue staining and MR scans of CSPIO-labeled NPCCs were performed. In vivo, we transplanted 2000 CSPIO-labeled NPCCs under the kidney capsule of nondiabetic nude mice. Recipients were scanned with 7.0T MRI. Grafts were removed for histology with insulin and Prussian blue staining. After being incubated overnight with CSPIO, NPCCs showed positive iron staining and appeared as dark spots on MR scans. After transplantation of CSPIO-labeled NPCCs, persistent hypointense areas were observed at recipients' implant sites for up to 54 days. Moreover, histology showed colocalization of the insulin and iron staining in 15-, 51- and 55-day NPCC grafts. Our results indicate that transplanted NPCCs survived and differentiated to β cells after transplantation, and that MRI is a useful tool for the detection and monitoring of CSPIO-labeled NPCC grafts. |
Author | Li, Wan-Chun Wang, Jiun-Jie Shen, Chia-Rui Kao, Chen-Wei Chen, Chen-Ling Juang, Jyuhn-Huarng Wu, Shu-Ting Tsai, Zei-Tsan Lin, Sung-Han Chen, Chen-Yi |
AuthorAffiliation | 2 Department of Medicine, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan 3 Department of Medical Imaging and Radiological Sciences, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan; jiunjie.wang@gmail.com (J.-J.W.); image.lin@gmail.com (S.-H.L.) 6 Institute of Oral Biology, School of Dentistry, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan; wcli@ym.edu.tw 7 Molecular Imaging Center, Chang Gung Memorial Hospital, Taoyuan 33302, Taiwan; zeitsan@ms9.hinet.net 5 Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan; crshen@mail.cgu.edu.tw (C.-R.S.); proteinwhite@livemail.tw (S.-T.W.) 1 Division of Endocrinology and Metabolism, Department of Internal Medicine and Center for Tissue Engineering, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan; Je3474@gmail.com (C.-Y.C.); lian8807111@gmail.com (C.-W.K.); jenny74513@gmail.com (C.-L.C.) 4 Department of Diagnostic Radiology, |
AuthorAffiliation_xml | – name: 2 Department of Medicine, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan – name: 4 Department of Diagnostic Radiology, Chang Gung Memorial Hospital, Keelung 20401, Taiwan – name: 7 Molecular Imaging Center, Chang Gung Memorial Hospital, Taoyuan 33302, Taiwan; zeitsan@ms9.hinet.net – name: 3 Department of Medical Imaging and Radiological Sciences, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan; jiunjie.wang@gmail.com (J.-J.W.); image.lin@gmail.com (S.-H.L.) – name: 1 Division of Endocrinology and Metabolism, Department of Internal Medicine and Center for Tissue Engineering, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan; Je3474@gmail.com (C.-Y.C.); lian8807111@gmail.com (C.-W.K.); jenny74513@gmail.com (C.-L.C.) – name: 5 Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan; crshen@mail.cgu.edu.tw (C.-R.S.); proteinwhite@livemail.tw (S.-T.W.) – name: 6 Institute of Oral Biology, School of Dentistry, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan; wcli@ym.edu.tw |
Author_xml | – sequence: 1 givenname: Jyuhn-Huarng orcidid: 0000-0003-1544-6059 surname: Juang fullname: Juang, Jyuhn-Huarng – sequence: 2 givenname: Jiun-Jie surname: Wang fullname: Wang, Jiun-Jie – sequence: 3 givenname: Chia-Rui orcidid: 0000-0002-8386-3965 surname: Shen fullname: Shen, Chia-Rui – sequence: 4 givenname: Chen-Yi surname: Chen fullname: Chen, Chen-Yi – sequence: 5 givenname: Chen-Wei surname: Kao fullname: Kao, Chen-Wei – sequence: 6 givenname: Chen-Ling surname: Chen fullname: Chen, Chen-Ling – sequence: 7 givenname: Sung-Han orcidid: 0000-0003-1384-4037 surname: Lin fullname: Lin, Sung-Han – sequence: 8 givenname: Shu-Ting surname: Wu fullname: Wu, Shu-Ting – sequence: 9 givenname: Wan-Chun orcidid: 0000-0003-0481-4215 surname: Li fullname: Li, Wan-Chun – sequence: 10 givenname: Zei-Tsan surname: Tsai fullname: Tsai, Zei-Tsan |
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Snippet | Neonatal pancreatic cell clusters (NPCCs) are potential tissues for the treatment of diabetes. Different from adult cells, they continuously proliferate and... |
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SubjectTerms | Chitosan Clusters Contrast agents Grafting Histology Insulin Iron Iron oxides Laboratory animals Magnetic resonance imaging Molecular weight Nanoparticles Pigments Potassium Staining Swine Transplantation Transplants & implants |
Title | Magnetic Resonance Imaging of Transplanted Porcine Neonatal Pancreatic Cell Clusters Labeled with Chitosan-Coated Superparamagnetic Iron Oxide Nanoparticles in Mice |
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