1 alpha,25-dihydroxyvitamin D-3 protects human keratinocytes from apoptosis by the formation of sphingosine-1-phosphate

Citation
M. Manggau et al., 1 alpha,25-dihydroxyvitamin D-3 protects human keratinocytes from apoptosis by the formation of sphingosine-1-phosphate, J INVES DER, 117(5), 2001, pp. 1241-1249
Citations number
51
Categorie Soggetti
Dermatology,"da verificare
Journal title
JOURNAL OF INVESTIGATIVE DERMATOLOGY
ISSN journal
0022202X → ACNP
Volume
117
Issue
5
Year of publication
2001
Pages
1241 - 1249
Database
ISI
SICI code
0022-202X(200111)117:5<1241:1ADPHK>2.0.ZU;2-4
Abstract
Owing to its ability to induce growth arrest and differentiation of keratin ocytes, 1 alpha ,25-dihydroxy-vitamin D-3 and its analogs are useful for th e treatment of hyperproliferative skin diseases, such as psoriasis vulgaris . It has been implicated that the la,25-dihydroxyvitamin D-3-induced differ entiation of keratinocytes is mediated, at least in part, by the formation of ceramides; however, ceramides have also been identified to induce apopto sis in many cells, including keratinocytes. Therefore, it was of interest t o investigate the influence of 1 alpha ,25-dihydroxyvitamin D3 on apoptosis in keratinocytes. Most interestingly, physiological concentrations of 1 al pha ,25-dihydroxyvitamin D3 did not induce apoptosis in keratinocytes, desp ite the formation of ceramides. Moreover, la.,25-dihydroxyvitamin D3 appear ed cytoprotective and made keratinocytes resistant to apoptosis induced by ceramides, ultraviolet irradiation, or tumor necrosis factor-m The cytoprot ective effect was accompanied by the formation of the sphingolipid breakdow n product sphingosine-1-phosphate, which prevented apoptosis in analogy to 1 alpha ,25-dihydroxyvitamin D3. The effect of 1 alpha ,25-dihydroxyvitamin D3 was specific as the almost inactive precursor cholecalciferol neither i nduced sphingosine-1-phosphate formation nor prevented cells from apoptosis . Besides this, the cytoprotective aptitude of la,25-dihydroxyvitamin D3 wa s completely abolished by the sphingosine kinase inhibitor N,N-dimethylsphi ngosine, which blocked sphingosine-1-phosphate formation. Moreover, sphingo sine-1-phosphate was able to restore the cytoprotective effect of la,25-dih ydroxyvitamin D3 in the presence of N,N-dimethylsphingosine. Taken together , here we report for the first time that la,25-dihydroxyvitamin D3 protects keratinocytes from apoptosis and additionally this cytoprotection is media ted via the formation of sphingosine-1-phosphate.