The Image–Histology Correlation of Subcutaneous mPEG-poly(Ala) Hydrogel-Embedded MIN6 Cell Grafts in Nude Mice

Author:

Juang Jyuhn-Huarng12ORCID,Chen Chen-Ling1,Kao Chen-Wei1,Chen Chen-Yi1,Shen Chia-Rui34ORCID,Wang Jiun-Jie56,Tsai Zei-Tsan7,Chu I-Ming8ORCID

Affiliation:

1. Division of Endocrinology and Metabolism, Department of Internal Medicine and Center for Tissue Engineering, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan

2. Department of Medicine, College of Medicine, Chang Gung University, Taoyuan 33305, Taiwan

3. Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan 33305, Taiwan

4. Department of Ophthalmology, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan

5. Department of Medical Imaging and Radiological Sciences, College of Medicine, Chang Gung University, Taoyuan 33305, Taiwan

6. Department of Diagnostic Radiology, Chang Gung Memorial Hospital, Keelung 20401, Taiwan

7. Molecular Imaging Center, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan

8. Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300044, Taiwan

Abstract

Previously, we have successfully used noninvasive magnetic resonance (MR) and bioluminescence imaging to detect and monitor mPEG-poly(Ala) hydrogel-embedded MIN6 cells at the subcutaneous space for up to 64 days. In this study, we further explored the histological evolution of MIN6 cell grafts and correlated it with image findings. MIN6 cells were incubated overnight with chitosan-coated superparamagnetic iron oxide (CSPIO) and then 5 × 106 cells in the 100 μL hydrogel solution were injected subcutaneously into each nude mouse. Grafts were removed and examined the vascularization, cell growth and proliferation with anti-CD31, SMA, insulin and ki67 antibodies, respectively, at 8, 14, 21, 29 and 36 days after transplantation. All grafts were well-vascularized with prominent CD31 and SMA staining at all time points. Interestingly, insulin-positive cells and iron-positive cells were scattered in the graft at 8 and 14 days; while clusters of insulin-positive cells without iron-positive cells appeared in the grafts at 21 days and persisted thereafter, indicating neogrowth of MIN6 cells. Moreover, proliferating MIN6 cells with strong ki67 staining was observed in 21-, 29- and 36-day grafts. Our results indicate that the originally transplanted MIN6 cells proliferated from 21 days that presented distinctive bioluminescence and MR images.

Funder

Chang Gung Memorial Hospital, Taiwan

Chang Gung Memorial Hospital and National Tsing Hua University Joint Research Program CGMH-NTHU 2019, Taiwan

Chang Gung Memorial Hospital and National Tsing Hua University Joint Research Program CGMH-NTHU 2020, Taiwan

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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