Magnetic Resonance Imaging of Transplanted Porcine Neonatal Pancreatic Cell Clusters Labeled with Exendin-4-Conjugated Manganese Magnetism-Engineered Iron Oxide Nanoparticles.
Jyuhn-Huarng JuangJiun-Jie WangChia-Rui ShenSung-Han LinChen-Yi ChenChen-Wei KaoChen-Ling ChenShu-Ting WuZei-Tsan TsaiYun-Ming WangPublished in: Nanomaterials (Basel, Switzerland) (2022)
Recently, we have shown that manganese magnetism-engineered iron oxide nanoparticles (MnMEIO NPs) conjugated with exendin-4 (Ex4) act as a contrast agent that directly trace implanted mouse islet β-cells by magnetic resonance imaging (MRI). Here we further advanced this technology to track implanted porcine neonatal pancreatic cell clusters (NPCCs) containing ducts, endocrine, and exocrine cells. NPCCs from one-day-old neonatal pigs were isolated, cultured for three days, and then incubated overnight with MnMEIO-Ex4 NPs. Binding of NPCCs and MnMEIO-Ex4 NPs was confirmed with Prussian blue staining in vitro prior to the transplantation of 2000 MnMEIO-Ex4 NP-labeled NPCCs beneath the left renal capsule of six nondiabetic nude mice. The 7.0 T MRI on recipients revealed persistent hypointense areas at implantation sites for up to 54 days. The MR signal intensity of the graft on left kidney reduced 62-88% compared to the mirror areas on the contralateral kidney. Histological studies showed colocalization of insulin/iron and SOX9/iron staining in NPCC grafts, indicating that MnMEIO-Ex4 NPs were taken up by mature β-cells and pancreatic progenitors. We conclude that MnMEIO-Ex4 NPs are excellent contrast agents for detecting and long-term monitoring implanted NPCCs by MRI.
Keyphrases
- magnetic resonance imaging
- contrast enhanced
- induced apoptosis
- iron oxide nanoparticles
- cell cycle arrest
- magnetic resonance
- single cell
- computed tomography
- oxide nanoparticles
- endoplasmic reticulum stress
- endothelial cells
- pet imaging
- transcription factor
- risk assessment
- high intensity
- kidney transplantation
- case control