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Development and Application of a Semi quantitative Scoring Method for Ultrastructural Assessment of Acute Stress in Pancreatic Islets

Pancreas and islet transplantation outcomes are negatively impacted by injury to the endocrine cells from acute stress during donor death, organ procurement, processing, and transplant procedures. Here, we report a novel electron microscopy scoring system, the Newcastle Pancreas Endocrine Stress Sco...

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Bibliographic Details
Published in:Transplantation direct 2021-12, Vol.8 (1), p.e1271-e1271
Main Authors: Dyson, Nicola J., Kattner, Nicole, Honkanen-Scott, Minna, Hunter, Bethany, Doyle, Jennifer A., White, Kathryn, Davey, Tracey S., Ploeg, Rutger J., Bury, Yvonne A., Tiniakos, Dina G., Shaw, James A. M., Scott, William E.
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Language:English
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Summary:Pancreas and islet transplantation outcomes are negatively impacted by injury to the endocrine cells from acute stress during donor death, organ procurement, processing, and transplant procedures. Here, we report a novel electron microscopy scoring system, the Newcastle Pancreas Endocrine Stress Score (NPESS). NPESS was adapted and expanded from our previously validated method for scoring pancreatic exocrine acinar cells, yielding a 4-point scale (0-3) classifying ultrastructural pathology in endocrine cell nuclei, mitochondria, endoplasmic reticulum, cytoplasmic vacuolization, and secretory granule depletion, with a maximum additive score of 15. We applied NPESS in a cohort of deceased organ donors after brainstem (DBD) and circulatory (DCD) death with a wide range of cold ischemic times (3.6-35.9 h) including 3 donors with type 1 and 3 with type 2 diabetes to assess islets in situ (n = 30) in addition to pancreata (n = 3) pre- and postislet isolation. In DBD pancreata, NPESS correlated with cold ischemic time (head: r = 0.55;  = 0.02) and mirrored exocrine score (r = 0.48;  = 0.01). When stratified by endocrine phenotype, cells with granules of heterogeneous morphology had higher scores than α, β, and δ cells (  
ISSN:2373-8731
2373-8731
DOI:10.1097/TXD.0000000000001271