Continuous vs. discontinuous purification of isolated human islets: functional and morphological comparison.

Front Endocrinol (Lausanne)

Department of Surgery, Cliniques Universitaires Saint Luc, Université Catholique de Louvain, Surgery and Abdominal Transplantation Unit, Brussels, Belgium.

Published: July 2023


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Article Abstract

Background: The COBE 2991 cell processor, commonly used for pancreatic islet isolation, is no longer distributed in Europe, leading to a search for alternative purification procedures with equivalent efficacy. The aim of this study was to evaluate the efficacy of an alternative method based on the discontinuous purification of islets.

Methods: The conventional isolation procedure using a standard continuous islet purification with COBE 2991 of = 4 human pancreas was compared to = 8 procedures using a discontinuous purification with a "bottle" method from donors of similar characteristics. Islet equivalents, purity, and dynamic glucose-stimulated insulin secretion were evaluated.

Results: A similar islet yield was obtained using continuous vs. discontinuous purification methods (76,292.5 ± 40,550.44 vs. 79,625 ± 41,484.46 islet equivalents, = 0.89). Islets from both groups had similar purity (78.75% ± 19.73% vs. 55% ± 18.16%, = 0.08) and functionality both in terms of stimulation index (3.31 ± 0.83 vs. 5.58 ± 3.38, = 0.22) and insulin secretion (1.26 ± 0.83 vs. 1.53 ± 1.40 mean AUC, = 0.73). Moreover, the size of the islets was significantly larger in the discontinuous vs. continuous purification group (19.2% ± 10.3% vs. 45.4% ± 18.8% of islets less than 100 µm, = 0.0097 and 23.7% ± 5.3% vs. 15.6% ± 5.8% of 200-250 µm islet size, = 0.03).

Conclusion: Compared to the conventional purification procedure, discontinuous purification with a bottle method shows similar results with regard to isolation yield and islet secretory function. Furthermore, this alternative technique allows for obtaining larger islets.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348810PMC
http://dx.doi.org/10.3389/fendo.2023.1195545DOI Listing

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