# Isolation of feline islets of Langerhans by selective osmotic shock produces glucose responsive islets

**Authors:** Lauren T. Porter, Christopher A. Adin, Chiquitha D. Crews, Jocelyn Mott, Chen Gilor

PMC · DOI: 10.3389/fvets.2024.1365611 · Frontiers in Veterinary Science · 2024-03-07

## TL;DR

A new method for isolating feline islets using osmotic shock improves their glucose responsiveness, making them useful for diabetes research.

## Contribution

A novel selective osmotic shock protocol for isolating functional feline islets with improved glucose responsiveness.

## Key findings

- Islet yield was moderate and morphology was excellent across protocol treatments.
- The 600 mmol/L glucose solution with 20 min incubation produced the highest glucose-stimulated insulin secretion stimulation index.
- Glucose responsiveness was successfully demonstrated, enabling future in vitro studies on feline islets.

## Abstract

Pancreatic islet isolation is essential for studying islet physiology, pathology, and transplantation, and feline islets could be an important model for human type II diabetes mellitus (T2D). Traditional isolation methods utilizing collagenases inflict damage and, in cats, may contribute to the difficulty in generating functional islets, as demonstrated by glucose-stimulated insulin secretion (GSIS). GLUT2 expression in β cells may allow for adaptation to hyperosmolar glucose solutions while exocrine tissue is selectively disrupted.

Here we developed a protocol for selective osmotic shock (SOS) for feline islet isolation and evaluated the effect of different hyperosmolar glucose concentrations (300 mmol/L and 600 mmol/L) and incubation times (20 min and 40 min) on purity, morphology, yield, and GSIS.

Across protocol treatments, islet yield was moderate and morphology excellent. The treatment of 600 mmol/L glucose solution with 20 min incubation resulted in the highest stimulation index by GSIS.

Glucose responsiveness was demonstrated, permitting future in vitro studies. This research opens avenues for understanding feline islet function and transplantation possibilities and enables an additional islet model for T2D.

## Linked entities

- **Proteins:** SLC2A2 (solute carrier family 2 member 2)
- **Chemicals:** glucose (PubChem CID 5793)
- **Diseases:** type II diabetes mellitus (MONDO:0005148), T2D (MONDO:0005148)

## Full-text entities

- **Genes:** GLUT2 [NCBI Gene 100142681], insulin [NCBI Gene 493804]
- **Diseases:** T2D (MESH:D003924)
- **Chemicals:** Glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10954776/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC10954776/full.md

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Source: https://tomesphere.com/paper/PMC10954776