PURPOSE OF REVIEW: Type 1 and type 2 diabetes mellitus represent a widespread metabolic disorder, related to autoimmune β-cell destruction and insulin resistance, leading to β-cell dysfunction, respectively, that are associated with severe chronic complications with irreversible multiorgan morphological and functional damage. Conventional treatment, based on exogenous insulin or oral agents may control and delay but not prevent the disease complications, which has lead, so far, to a steady increase in mortality and morbidity. β-Cell substitution cell therapy, initially pursued by whole pancreatic and isolated islet transplantation, with scarce and limited efficiency, now is looking at the new technologies for cell and molecular therapy for diabetes, based on stem cells. RECENT FINDINGS: Pancreatic endocrine cells regeneration might replenish the destroyed β-cell pool, with neogenerated β-cell derived from pancreatic and extrapancreatic stem cell sources. Additionally, embryonic or adult stem cells derived from different cell lineages, and able to differentiate into β-like cell elements, may not only restore the original insulin secretory patterns but also exert the immunomodulatory effects aimed at interrupting the β-cell-directed autoimmune destruction vicious cycle. SUMMARY: These new strategies may, one day, provide for the final cure of diabetes mellitus.
PURPOSE OF REVIEW: Type 1 and type 2 diabetes mellitus represent a widespread metabolic disorder, related to autoimmune β-cell destruction and insulin resistance, leading to β-cell dysfunction, respectively, that are associated with severe chronic complications with irreversible multiorgan morphological and functional damage. Conventional treatment, based on exogenous insulin or oral agents may control and delay but not prevent the disease complications, which has lead, so far, to a steady increase in mortality and morbidity. β-Cell substitution cell therapy, initially pursued by whole pancreatic and isolated islet transplantation, with scarce and limited efficiency, now is looking at the new technologies for cell and molecular therapy for diabetes, based on stem cells. RECENT FINDINGS:Pancreatic endocrine cells regeneration might replenish the destroyed β-cell pool, with neogenerated β-cell derived from pancreatic and extrapancreatic stem cell sources. Additionally, embryonic or adult stem cells derived from different cell lineages, and able to differentiate into β-like cell elements, may not only restore the original insulin secretory patterns but also exert the immunomodulatory effects aimed at interrupting the β-cell-directed autoimmune destruction vicious cycle. SUMMARY: These new strategies may, one day, provide for the final cure of diabetes mellitus.
Authors: Anna Munder; Liron L Israel; Shirin Kahremany; Rina Ben-Shabat-Binyamini; Charles Zhang; Michal Kolitz-Domb; Olga Viskind; Anna Levine; Hanoch Senderowitz; Steven Chessler; Jean-Paul Lellouche; Arie Gruzman Journal: ACS Appl Mater Interfaces Date: 2017-01-03 Impact factor: 9.229
Authors: Alexandra M Smink; Shiri Li; Don T Hertsig; Bart J de Haan; Leendert Schwab; Aart A van Apeldoorn; Eelco de Koning; Marijke M Faas; Jonathan R T Lakey; Paul de Vos Journal: Transplantation Date: 2017-04 Impact factor: 4.939
Authors: Giulia Donadel; Donatella Pastore; David Della-Morte; Barbara Capuani; Marco F Lombardo; Francesca Pacifici; Marco Bugliani; Fabio A Grieco; Piero Marchetti; Davide Lauro Journal: Int J Mol Sci Date: 2017-10-25 Impact factor: 5.923
Authors: Robert C Rennert; Michael Januszyk; Michael Sorkin; Melanie Rodrigues; Zeshaan N Maan; Dominik Duscher; Alexander J Whittam; Revanth Kosaraju; Michael T Chung; Kevin Paik; Alexander Y Li; Michael Findlay; Jason P Glotzbach; Atul J Butte; Geoffrey C Gurtner Journal: Nat Commun Date: 2016-06-21 Impact factor: 14.919