In Vitro Human Fetal Pancreatic Islets to Redefine Pancreatic Research

• Published in: Curēus (Palo Alto, CA) CA), 2023-08, Vol.15 (8), p.e43244-e43244
• Main Authors: Rout, Sipra, Amirtham, Soosai Manickam, Prasad, Mythraeyee, Cherian, Anne George, B, Sandya Rani, Sudhakar, Yesudas, Prince, Neetu
• Format: Article
• Language: English
• Subjects: Alcohol; Anatomy; Antibodies; Cold; Diabetes; Endocrinology/Diabetes/Metabolism; Enzymes; Fetuses; Glucagon; Glucose; Insulin; Invoices; Medical research; Microscopy; Pancreas; Polypeptides; Stem cells; Transplantation
• ISSN: 2168-8184; 2168-8184
• DOI: 10.7759/cureus.43244

Background:In vitro studies with human fetal islets of different gestational ages (GA) would be a great tool to generate information on the developmental process of the islets as this would help to recontextualize diabetes research and clinical practice. Pancreatic islets from human cadavers and other animal species are extensively researched to explore their suitability for islet transplantation procedure, one of the upcoming treatment strategies for insulin-dependent diabetes mellitus. Although human fetal islets are also considered for islet transplantation, ethical issues and limited knowledge constraints their use. The fetal islets could be explored to address the information lacunae on the maturity process of pancreatic islets and the endocrine-exocrine signaling mechanisms.Aim: This study aimed to assess the feasibility of isolating viable islets and study the cytoarchitecture of the fetal pancreas of GA 22-29 weeks, not reported otherwise.Methodology: Pancreas obtained from the aborted fetuses of GA 22-29 weeks were subjected to collagenase digestion and were further cultured to determine the viability in vitro. Parameters assessed were expression of markers for endocrine cell lineages and insulin release to glucose challenge.Results: Islets were viable in vitro and islets were shown to maintain cues for post-digestion re-aggregation and expansion in culture. The immunofluorescent staining showed islets of varying sizes, homogenous cell clusters aggregating to form heterogenous cell clusters, otherwise not reported for this GA. On stimulation with different concentrations of glucose (2.8 and 28 mM), the fetal islets in the culture exhibited insulin release, and this response confirmed their viability in vitro.Conclusion: Our findings showed that viable islets could be isolated and cultured in vitro for further in-depth studies to explore their proliferative potential as well as for the identification of pancreatic progenitors, a good strategy to take forward.