Literature DB >> 26377964

Optimization and Scale-up Isolation and Culture of Neonatal Porcine Islets: Potential for Clinical Application.

Cara Ellis1, James G Lyon, Gregory S Korbutt.   

Abstract

One challenge that must be overcome to allow transplantation of neonatal porcine islets (NPIs) to become a clinical reality is defining a reproducible and scalable protocol for the efficient preparation of therapeutic quantities of clinical grade NPIs. In our standard protocol, we routinely isolate NPIs from a maximum of four pancreases, requiring tissue culture in 16 Petri dishes (four per pancreas) in Ham's F10 and bovine serum albumin (BSA). We have now developed a scalable and technically simpler protocol that allows us to isolate NPIs from a minimum of 12 pancreases at a time by employing automated tissue chopping, collagenase digestion in a single vessel, and tissue culture/media changes in 75% fewer Petri dishes. For culture, BSA is replaced with human serum albumin and supplemented with Z-VAD-FMK general caspase inhibitor and a protease inhibitor cocktail. The caspase inhibitor was added to the media for only the first 90 min of culture. NPIs isolated using the scalable protocol had significantly more cellular insulin recovered (56.9 ± 1.4 µg) when compared to the standard protocol (15.0 ± 0.5 µg; p < 0.05). Compared to our standard protocol, recovery of β-cells (6.0 × 10(6) ± 0.2 vs. 10.0 × 10(6) ± 0.4; p < 0.05) and islet equivalents (35,135 ± 186 vs. 41,810 ± 226; p < 0.05) was significantly higher using the scalable protocol. During a static glucose stimulation assay, the SI of islets isolated by the standard protocol were significantly lower than the scale-up protocol (4.3 ± 0.2 vs. 5.5 ± 0.1; p < 0.05). Mice transplanted with NPIs using the scalable protocol had significantly lower blood glucose levels than the mice that receiving NPIs from the standard protocol (p < 0.01) and responded significantly better to a glucose tolerance test. Based on the above findings, this improved simpler scalable protocol is a significantly more efficient means for preparing therapeutic quantities of clinical grade NPIs.

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Year:  2015        PMID: 26377964     DOI: 10.3727/096368915X689451

Source DB:  PubMed          Journal:  Cell Transplant        ISSN: 0963-6897            Impact factor:   4.064


  8 in total

1.  Optimization of Nano-encapsulation on Neonatal Porcine Islet-like Cell Clusters Using Polymersomes.

Authors:  Sang Hoon Lee; Hyun-Ouk Kim; Jung-Taek Kang
Journal:  Nanoscale Res Lett       Date:  2021-03-31       Impact factor: 4.703

Review 2.  Advances in islet encapsulation technologies.

Authors:  Tejal Desai; Lonnie D Shea
Journal:  Nat Rev Drug Discov       Date:  2016-12-23       Impact factor: 84.694

3.  An islet maturation media to improve the development of young porcine islets during in vitro culture.

Authors:  Hien Lau; Nicole Corrales; Samuel Rodriguez; Colleen Luong; Frank Zaldivar; Michael Alexander; Jonathan R T Lakey
Journal:  Islets       Date:  2020-05-27       Impact factor: 2.694

Review 4.  Will Genetic Engineering Carry Xenotransplantation of Pig Islets to the Clinic?

Authors:  Elisabeth Kemter; Joachim Denner; Eckhard Wolf
Journal:  Curr Diab Rep       Date:  2018-09-18       Impact factor: 4.810

5.  Cost and Scalability Analysis of Porcine Islet Isolation for Islet Transplantation: Comparison of Juvenile, Neonatal and Adult Pigs.

Authors:  Rachel Vanderschelden; Mayilone Sathialingam; Michael Alexander; Jonathan R T Lakey
Journal:  Cell Transplant       Date:  2019-04-30       Impact factor: 4.064

6.  Comparison of Islet Characterization from Use of Standard Crude Collagenase to GMP-Grade Collagenase Enzyme Blends in Preweaned Porcine Islet Isolations.

Authors:  Nicole Corrales; Soomin Park; Hien Lau; Ivana Xu; Colleen Luong; Samuel Rodriguez; Johanna Mönch; Michael Alexander; Jonathan Rt Lakey
Journal:  Cell Transplant       Date:  2020 Jan-Dec       Impact factor: 4.064

7.  Butyrate and Class I Histone Deacetylase Inhibitors Promote Differentiation of Neonatal Porcine Islet Cells into Beta Cells.

Authors:  Yichen Zhang; Yutian Lei; Mohsen Honarpisheh; Elisabeth Kemter; Eckhard Wolf; Jochen Seissler
Journal:  Cells       Date:  2021-11-19       Impact factor: 6.600

8.  Differentiation of Microencapsulated Neonatal Porcine Pancreatic Cell Clusters in Vitro Improves Transplant Efficacy in Type 1 Diabetes Mellitus Mice.

Authors:  Gyeong-Jin Cheon; Heon-Seok Park; Eun-Young Lee; Min Jung Kim; Young-Hye You; Marie Rhee; Ji-Won Kim; Kun-Ho Yoon
Journal:  Diabetes Metab J       Date:  2022-02-07       Impact factor: 5.893

  8 in total

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