Xenograft of microencapsulated sertoli cells reverses T1DM in NOD mice by inducing neogenesis of beta-cells

Transplantation. 2010 Dec 27;90(12):1352-7. doi: 10.1097/tp.0b013e3181ffb9d2.

Abstract

Background: Sertoli cells (SCs) provide an immunoprotective environment to pancreatic islet grafts for treatment of insulin-dependent diabetes. Aim of this work was to verify whether intraperitoneal graft of SCs, enveloped in barium alginate-based microcapsules, would reverse overt spontaneous diabetes in nonobese diabetic (NOD) mice by eliciting generation of newly formed functional islets β-cells.

Methods: Microcapsules were prepared, according to our method, by a mono air-jet device system and thereafter examined as far as (a) SC morphology by light microscopy; (b) SC viability by fluorescence microscopy; (c) SC in vitro function; and (d) SC in vivo function, as quoted by diabetes reversal in the NOD mice, were concerned.

Results: SCs containing microcapsules exhibited excellent morphology, viability, and function, and when grafted into the NOD's, they induced stable reversion of the disease in 81% of the cases. The treated mice showed dramatic increase in regulatory T lymphocytes (Treg) when compared with control diabetic NOD's treated with empty capsules only. Histologic examination of pancreata retrieved from the SC-transplanted animals showed total disappearance of insulitis, with appearance of new islets, as shown by immunocytochemistry; restored ability of the islets to produce insulin, glucagon, and somatostatin; and finally, increased expression of key transcriptional factors such as neurogenin 3.

Conclusions: SCs, enveloped in barium alginate-based microcapsules, showed no long-term loss of their functional and morphological properties in vitro or in vivo. Xenograft of microencapsulated-SC-induced reversal of spontaneous diabetes in the majority of the treated NOD mice, based on SC-related powerful immunomodulatory and pro-β-cell regeneration properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantibodies / blood
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Type 1 / surgery*
  • Eye Proteins / genetics
  • Glucagon / blood
  • Glucagon / immunology
  • Homeodomain Proteins / genetics
  • Immunohistochemistry
  • Insulin / blood
  • Insulin Antibodies / blood
  • Insulin-Secreting Cells / pathology*
  • Insulin-Secreting Cells / physiology
  • Male
  • Mice
  • Mice, Inbred NOD
  • Nerve Tissue Proteins / genetics
  • PAX6 Transcription Factor
  • Paired Box Transcription Factors / genetics
  • Pancreatitis-Associated Proteins
  • Polymerase Chain Reaction
  • Proteins / genetics
  • Proto-Oncogene Proteins c-kit / genetics
  • Repressor Proteins / genetics
  • Sertoli Cells / cytology
  • Sertoli Cells / transplantation*
  • Somatostatin / blood
  • Testis / cytology
  • Trans-Activators / genetics
  • Transplantation, Heterologous

Substances

  • Autoantibodies
  • Basic Helix-Loop-Helix Transcription Factors
  • Blood Glucose
  • Eye Proteins
  • Homeodomain Proteins
  • Insulin
  • Insulin Antibodies
  • Nerve Tissue Proteins
  • Neurod1 protein, mouse
  • Neurog3 protein, mouse
  • PAX6 Transcription Factor
  • Paired Box Transcription Factors
  • Pancreatitis-Associated Proteins
  • Pax4 protein, mouse
  • Pax6 protein, mouse
  • Proteins
  • Reg3b protein, mouse
  • Repressor Proteins
  • Trans-Activators
  • pancreatic and duodenal homeobox 1 protein
  • Somatostatin
  • Glucagon
  • Proto-Oncogene Proteins c-kit