Impact of integrin-matrix matching and inhibition of apoptosis on the survival of purified human beta-cells in vitro
Adult
0301 basic medicine
Niacinamide/pharmacology
Integrins
Cell Survival
Green Fluorescent Proteins
Apoptosis
Cell Separation
Transfection
Polymerase Chain Reaction
Recombinant Proteins/analysis
Islets of Langerhans
03 medical and health sciences
Genes, Reporter
info:eu-repo/classification/ddc/616
info:eu-repo/classification/ddc/617
Animals
Humans
Insulin
Islets of Langerhans/ cytology
Cells, Cultured
Aged
ddc:616
Cell Survival/drug effects/ physiology
Extracellular Matrix/ physiology
Insulin/genetics
Fibroblasts
Middle Aged
Flow Cytometry
Caspase Inhibitors
Rats
Extracellular Matrix
3. Good health
Integrins/ genetics/ physiology
Luminescent Proteins
Fibroblasts/cytology
Caspases/antagonists & inhibitors
Apoptosis/ physiology
Culture Media, Conditioned
Luminescent Proteins/genetics
Cell Separation/methods
DOI:
10.1007/s00125-002-0840-7
Publication Date:
2003-01-16T15:33:36Z
AUTHORS (11)
ABSTRACT
Human islet cells survive poorly in culture and are overgrown by non-endocrine cells. The aims of this study were to sort human beta cells and to develop approaches for their improved survival in culture.Human islets were infected with recombinant adenovirus expressing green fluorescent protein (GFP) under the control of the rat insulin promoter such that only beta cells expressed GFP. GFP-positive beta cells were sorted by flow cytometry, and expression of select integrins evaluated by RT-PCR. Beta cells were cultured on different extracellular matrices for up to 15 days. Apoptosis was measured by annexin V binding and ELISA. Insulin secretion was measured by ELISA.Sorted beta cells survived less well in culture than unsorted islet cells. This did not appear to be due to adenoviral infection and/or GFP expression. Purified beta cells expressed the integrins alpha 3, alpha 5, alpha 6, alpha V, beta1, but not beta 4. Of the various matrices tested, sorted beta cells attached and spread best on a lawn of lysed human bladder carcinoma cells (5637 cells). However, survival remained poor. Cell death was decreased but not prevented by continued presence of 10 mmol/l nicotinamide and apoptosis decreased by 24 h incubation with 20 micromol/l Z-VAD. Insulin secretion was maintained over 6 days following treatment with both agents.Purification of human beta cells induces marked apoptosis limiting their function and survival in vitro. This was improved by matching the extracellular matrix to the specific expression of integrins and by addition of nicotinamide and Z-VAD.
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