Literature DB >> 17269445

The use of the BD oxygen biosensor system to assess isolated human islets of langerhans: oxygen consumption as a potential measure of islet potency.

Chris Fraker1, Mark R Timmins, Richard D Guarino, Perry D Haaland, Hirohito Ichii, Damaris Molano, Antonello Pileggi, Raffaella Poggioli, Sharon C Presnell, Luca Inverardi, Mitra Zehtab, Camillo Ricordi.   

Abstract

The measurement of cellular oxygen consumption rate (OCR) is a potential tool for the assessment of metabolic potency of isolated islets of Langerhans prior to clinical transplantation. We used a commercially available 96-well plate fluoroprobe, the BD Oxygen Biosensor System (OBS), to estimate OCR in 27 human islet preparations, and compared these results to those of concurrent mouse transplantations. OCR was estimated both from the dO2 at steady state and from the transient rate of change of dO2 during the initial culture period immediately after seeding ("dO2 slope"). To demonstrate the validity of the OBS-derived values, it was shown that they scaled linearly with islet equivalent number/DNA concentration and with each other. These measurements were obtained for each preparation of islets incubated in media supplemented with either low (2.2 mM) or high (22 mM) glucose. Concurrently, one to three athymic nude mice were transplanted with 2,000 IEQs under the kidney capsule. The OCR Index, defined as the ratio of the DNA-normalized "dO2 slope" in high glucose to that in low glucose, proved highly predictive of mouse transplant results. Of the 69 mice transplanted, those receiving islets where the OCR Index exceeded 1.27 were 90% likely to reverse within 3 days, whereas those receiving islets with an OCR Index below 1.27 took significantly longer, often failing to reverse at all over a 35-day time period. These results suggest that the OBS could be a useful tool for the pretransplant assessment of islet cell potency.

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Year:  2006        PMID: 17269445     DOI: 10.3727/000000006783981440

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


  24 in total

1.  Automated, high-throughput assays for evaluation of human pancreatic islet function.

Authors:  Over Cabrera; M Caroline Jacques-Silva; Dora M Berman; Alberto Fachado; Felipe Echeverri; Ramon Poo; Aisha Khan; Norma S Kenyon; Camillo Ricordi; Per-Olof Berggren; Alejandro Caicedo
Journal:  Cell Transplant       Date:  2008       Impact factor: 4.064

2.  Detailed protocol for evaluation of dynamic perifusion of human islets to assess β-cell function.

Authors:  Kwamina Bentsi-Barnes; Máire E Doyle; Danny Abad; Fouad Kandeel; Ismail Al-Abdullah
Journal:  Islets       Date:  2011-09-01       Impact factor: 2.694

Review 3.  Re-engineering islet cell transplantation.

Authors:  Nicoletta Fotino; Carmen Fotino; Antonello Pileggi
Journal:  Pharmacol Res       Date:  2015-03-23       Impact factor: 7.658

4.  Aggregation of Engineered Human β-Cells Into Pseudoislets: Insulin Secretion and Gene Expression Profile in Normoxic and Hypoxic Milieu.

Authors:  Marie-José Lecomte; Séverine Pechberty; Cécile Machado; Sandra Da Barroca; Philippe Ravassard; Raphaël Scharfmann; Paul Czernichow; Bertrand Duvillié
Journal:  Cell Med       Date:  2016-08-12

5.  NADPH oxidase and PKC contribute to increased Na transport by the thick ascending limb during type 1 diabetes.

Authors:  Jing Yang; Jennifer S Pollock; Pamela K Carmines
Journal:  Hypertension       Date:  2011-12-27       Impact factor: 10.190

6.  A simplified approach to human islet quality assessment.

Authors:  Matthew S Hanson; Elisa E Park; Mallory L Sears; Krista K Greenwood; Juan Sebastian Danobeitia; Debra A Hullett; Luis A Fernandez
Journal:  Transplantation       Date:  2010-05-27       Impact factor: 4.939

7.  Prediction of marginal mass required for successful islet transplantation.

Authors:  Klearchos K Papas; Clark K Colton; Andi Qipo; Haiyan Wu; Rebecca A Nelson; Bernhard J Hering; Gordon C Weir; Maria Koulmanda
Journal:  J Invest Surg       Date:  2010-02       Impact factor: 2.533

8.  Genetic reduction of mitochondrial complex I function does not lead to loss of dopamine neurons in vivo.

Authors:  Hyung-Wook Kim; Won-Seok Choi; Noah Sorscher; Hyung Joon Park; François Tronche; Richard D Palmiter; Zhengui Xia
Journal:  Neurobiol Aging       Date:  2015-05-16       Impact factor: 4.673

9.  Mitochondrial complex I inhibition is not required for dopaminergic neuron death induced by rotenone, MPP+, or paraquat.

Authors:  Won-Seok Choi; Shane E Kruse; Richard D Palmiter; Zhengui Xia
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-23       Impact factor: 11.205

Review 10.  Islet assessment for transplantation.

Authors:  Klearchos K Papas; Thomas M Suszynski; Clark K Colton
Journal:  Curr Opin Organ Transplant       Date:  2009-12       Impact factor: 2.640

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