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Difference between revisions of "Hals 2013 J Diabetes Res"

From Bioblast
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|tissues=Islet cell;pancreas;thymus
|tissues=Islet cell;pancreas;thymus
|preparations=Intact cells
|preparations=Intact cells
|injuries=Hypoxia
|injuries=Ischemia-reperfusion
|couplingstates=ROUTINE, ETS
|couplingstates=ROUTINE, ETS
|substratestates=CI, ROX
|substratestates=CI, ROX
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
}}
}}

Revision as of 13:53, 16 June 2015

Publications in the MiPMap
Hals IK, Rokstad AM, Strand BL, Oberholzer J, Grill V (2013) Alginate microencapsulation of human islets does not increase susceptibility to acute hypoxia. J Diabetes Res 2013:374925.

Β» PMID: 24364039 Open Access

Hals IK, Rokstad AM, Strand BL, Oberholzer J, Grill V (2013) J Diabetes Res

Abstract: Islet transplantation in diabetes is hampered by the need of life-long immunosuppression. Encapsulation provides partial immunoprotection but could possibly limit oxygen supply, a factor that may enhance hypoxia-induced beta cell death in the early post-transplantation period. Here we tested susceptibility of alginate microencapsulated human islets to experimental hypoxia (0.1-0.3 % O2 for 8 h, followed by re-oxygenation) on viability and functional parameters. Hypoxia reduced viability as measured by MTT by 33.8 Β± 3.5 % in encapsulated and 42.9 Β± 5.2 % in non-encapsulated islets (p < 0.2). Non-encapsulated islets released 37.7% (median) more HMGB1 compared to encapsulated islets after hypoxic culture conditions (p < 0.001). Glucose-induced insulin release was marginally affected by hypoxia. Basal oxygen consumption was equally reduced in encapsulated and non-encapsulated islets, by 22.0 Β± 6.1 % vs. 24.8 Β± 5.7 %. Among 27 tested cytokines/chemokines, hypoxia increased the secretion of IL-6 and IL-8/CXCL8 in both groups of islets whereas an increase of MCP-1/CCL2 was seen only with non-encapsulated islets. Conclusion: alginate microencapsulation of human islets does not increase susceptibility to acute hypoxia. This is a positive finding in relation to potential use of encapsulation for islet transplantation. β€’ Keywords: Human islets, Microencapsulation, Hypoxia, Viability, Oxygen consumption, Insulin release, Cytokine/chemokine secretion

β€’ O2k-Network Lab: NO Trondheim Grill V


Labels: MiParea: Respiration, mt-Medicine 

Stress:Ischemia-reperfusion  Organism: Human  Tissue;cell: Islet cell;pancreas;thymus  Preparation: Intact cells 


Coupling state: ROUTINE, ETS"ETS" is not in the list (LEAK, ROUTINE, OXPHOS, ET) of allowed values for the "Coupling states" property. 

HRR: Oxygraph-2k