In vivo and in vitro data obtained in rodents indicate that beta-cells
can trigger efficient repair mechanisms following non-lethal injury,
Recent observations suggest that human pancreatic islets are more resi
stant than rodent islets to damage by alkylating agents, free oxygen r
adicals, nitric oxide and cytokines, This increased resistance to inju
ry is associated with higher expression of heat shock protein 70, cata
lase and superoxide dismutase, These findings emphasise the potential
relevance of beta-cell repair and/or defence mechanisms in the develop
ment of human IDDM.