Transplantation of rat pancreatic islets vitrified-warmed on the nylon mesh device and the silk fibroin sponge disc

Islets. 2020 Nov 1;12(6):145-155. doi: 10.1080/19382014.2020.1849928. Epub 2020 Dec 8.

Abstract

We report the adaptability of rat islets vitrified-warmed on nylon mesh (NM) device or silk fibroin (SF) sponge disc for the normalization of the blood glucose level in rat models of diabetes. One-hundred rat islets were cryopreserved according to a minimum volume cooling protocol on an NM device or a solid surface vitrification protocol on an SF sponge disc. The recovery rate (97.1% vs. 93.8%), the viability (77.9% vs. 74.4%), and the stimulation index (4.7 vs. 4.2) in glucose-stimulated insulin secretion (GSIS) assay of the post-warm islets were comparable between the NM vitrification and the SF vitrification groups. The viability and the stimulation index of the fresh control islets were identified to be 97.5% and 6.5, respectively. Eight hundred islets from the NM or the SF vitrification group or the fresh control group were transplanted beneath the kidney capsule of a streptozotocin-induced diabetic rat (blood glucose level > 350 mg/dl). Within 3 weeks after transplantation, the acquisition of euglycemia (< 200 mg/dl) was observed in recipient rats (80.0-83.3%). An intraperitoneal glucose tolerance test on Day-30 and Day-60 showed similar 2-h responses to the glucose uptake of cured rats among the compared groups. Moreover, the successful engraftment of transplants was confirmed by the Day-70 nephrectomy through the subsequent diabetes reversal and histological evaluation. Thus, large quantities of rat islets vitrified-warmed on an NM device or an SF sponge disc were proven to be fully functional both in vitro and in vivo, due to the GSIS and syngeneic transplantation, respectively.

Keywords: GSIS; Rat islets; nylon mesh; silk fibroin sponge; subrenal transplantation; vitrification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Fibroins*
  • Insulin
  • Islets of Langerhans Transplantation*
  • Islets of Langerhans*
  • Nylons
  • Rats
  • Surgical Mesh
  • Vitrification

Substances

  • Insulin
  • Nylons
  • Fibroins

Grants and funding

This study was supported by Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science [JSPS; 16K07985 and 20K06364 to S.H], a grant of General Collaborative Project from the National Institute for Physiological Science, Japan [NIPS; No.139 to S.H.], and a grant of Leading Advanced Projects for Medical Innovation from Japan Agency for Medical Research and Development [LEAP/AMED; JP18gm0010002 to M.H.]. K.N-I. and T.Y. were recipients from Kaneko-Hachiro Scholarship Foundation and Yoshida Scholarship Foundation, respectively.