Lefebvre D, Boney C M, Ketelslegers J M, Thissen J P
Diabetes and Nutrition Unit, Université Catholique de Louvain, Brussels, Belgium.
FEBS Lett. 1999 Apr 23;449(2-3):284-8. doi: 10.1016/s0014-5793(99)00419-6.
The mechanisms responsible for the resistance to the anabolic actions of IGF-I induced by zinc deficiency are not understood. We showed that zinc chelation by DTPA (diethylenetriaminepenta-acetic acid) inhibits [3H]thymidine incorporation stimulated by IGF-I in Rat-1 fibroblasts. This inhibition was specific of zinc chelation since it was prevented by the addition of zinc to DTPA. The stimulation of MAPK, which is crucial for the [3H]thymidine incorporation induced by IGF-I in Rat-1 cells, was partially blunted by DTPA. Therefore, the inhibition of the mitogenic action of IGF-I in Rat-1 fibroblasts by DTPA is potentially caused by decreased MAPK activation by IGF-I.