Affiliation: | (1) Instituto de Investigaciones Biomédicas (CSIC), C/ Arturo Duperier 4, 28029 Madrid, Spain;(2) Research Unit, Hospital Universitario de Canarias, Ofra s/n-La Cuesta, 38320 La Laguna, Spain;(3) National Institute for Medical Research, Yeast Genetics, The Ridgeway, Mill Hill, NW7 1AA London, United Kingdom |
Abstract: | The immunosuppressants tacrolimus (FK506) and cyclosporin A (CsA) have increased the survival rates in organ transplantation. Both drugs inhibit the protein phosphatase calcineurin (CaN) in activated T cells, exhibiting similar side-effects. Diabetes is observed more often in FK506 than CsA therapy, probably due to inhibition of new molecular targets other than CaN. We studied FK506 toxicity in mammalian cells. FK506, but not CsA, regulated p38 activation by osmotic stress, and decreased viability in osmostressed cells. In addition, FK506 treatment strongly increased the phosphorylation of the eukaryotic initiation factor-2a (eIF-2a) subunit. eIF-2a phosphorylation, p38 inhibition and cell lethality were relieved by addition of excess amino acids to the medium, suggesting that amino acid availability mediated FK506 toxicity. Therefore, these FK506-dependent responses could be relevant to the non-therapeutic effects of FK506 therapy.Received 16 October 2003; received after revision 8 January 2004; accepted 14 January 2004 |