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.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117 J+Dermatol+Sci
2015 ; 79
(3
): 229-34
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Sphingosine kinase 1 activation enhances epidermal innate immunity through
sphingosine-1-phosphate stimulation of cathelicidin production
#MMPMID26113114
Jeong SK
; Kim YI
; Shin KO
; Kim BW
; Lee SH
; Jeon JE
; Kim HJ
; Lee YM
; Mauro TM
; Elias PM
; Uchida Y
; Park K
J Dermatol Sci
2015[Sep]; 79
(3
): 229-34
PMID26113114
show ga
BACKGROUND: The ceramide metabolite, sphingosine-1-phosphate (S1P), regulates
multiple cellular functions in keratinocytes (KC). We recently discovered that
production of a key innate immune element, cathelicidin antimicrobial peptide
(CAMP), is stimulated via a NF-?B-dependent mechanism that is activated by S1P
when S1P is generated by sphingosine kinase (SPHK) 1. OBJECTIVE: We investigated
whether pharmacological modulation of SPHK1 activity, using a novel synthetic
SPHK1 activator, (S)-methyl 2-(hexanamide)-3-(4-hydroxyphenyl) propanoate (MHP),
stimulates CAMP expression. METHODS: MHP-mediated changes in both S1P and CAMP
downstream mediators were analyzed in normal cultured human KC by qRT-PCR,
Western immunoblot, ELISA, confocal microscopy for immunohistochemistry, HPLC and
ESI-LC/MS/MS, and microbial pathogen invasion/colonization in a human epidermal
organotypic model. RESULTS: Treatment with MHP directly activated SPHK1 and
increased cellular S1P content in normal cultured human KC. Because MHP did not
inhibit S1P lyase activity, which hydrolyses S1P, augumented S1P levels could be
attributed to increased synthesis rather than blockade of S1P degradation. Next,
we found that exogenous MHP significantly stimulated CAMP mRNA and protein
production in KC, increases that were significantly suppressed by siRNA directed
against SPHK1, but not by a scrambled control siRNA. NF-?B activation, assessed
by nuclear translocation of NF-?B, occurred in cells following incubation with
MHP. Conversely, pretreatment with a specific inhibitor of SPHK1 decreased
MHP-induced nuclear translocation of NF-?B, and significantly attenuated the
MHP-mediated increase in CAMP production. Finally, topical MHP significantly
suppressed invasion of the virulent Staphylococcus aureus into murine skin
explants. CONCLUSION: MHP activation of SPHK1, a target enzyme of CAMP
production, can stimulate innate immunity.