4.7 Article

Synthetic matrix of polyether-polyurethane as a biological platform for pancreatic regeneration

Journal

LIFE SCIENCES
Volume 176, Issue -, Pages 67-74

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.lfs.2017.03.015

Keywords

Sponge implant; Diabetes; Scaffold; Biomaterial; Human adipose stem cells; Insulin-producing cell

Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [481659/2012-9]
  2. Fundacao de Amparo a Pesquisa de Minas Gerais (FAPEMIG) [APQ-01461/12]

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Aims: Several alternative cellular approaches using biomaterials to host insulin-producing cells derived from stem cells have been developed to overcome the limitations of type 1 diabetes treatment (exogenous insulin injection). However, none seem to fulfill all requirements needed to induce pancreatic cells successful colonization of the scaffolds. Here, we report a polymeric platform adherent to the native mice pancreas filled with human adipose stem cells (hASCs) that was able to induce growth of pancreatic parenchyma. Main methods: Synthetic polyether-polyurethane discs were placed adjacent to pancreas of normoglycemic and streptozotocin-induced diabetic mice. At day 4 post implantation, 1 x 10(6) hASCs were injected intra-implant in groups of normoglycemic and diabetic mice. Immunohistochemistry analysis of the implants was performed to identify insulin positive cells in the newly formed tissue. In addition, metabolic, inflammatory and angiogenic parameters were carried out in those mice. Key findings: This study provides evidence of the ability of a biohybrid device to induce the growth of differentiated pancreas parenchyma in both normoglycemic and streptozotocin-induced diabetic mice as detected by histological analysis. Glucose metabolism and body weight of hyperglycemic mice bearing hASCs implants improved. Significance: The synthetic porous scaffold bearing hASC cells placed adjacent to the native animal pancreas exhibits the potential to be exploited in future cell-based type 1 diabetes therapies. (C) 2017 Elsevier Inc. All rights reserved.

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