Gentiana lutea Extract Modulates Ceramide Synthesis in Primary and Psoriasis-Like Keratinocytes

. 2020 Apr 16 ; 25 (8) : . [epub] 20200416

Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid32316273

Grantová podpora
ZF4399503MD7 Federal Ministry for Economic Affairs and Energy
19-09135J the Czech Science Foundation
SVV 260 401 Charles University

Gentiana lutea is a bitter herb that is traditionally used to improve gastric disorders. Recently, we have shown that Gentiana lutea extract (GE) also modulates the lipid metabolism of human keratinocytes in vitro and in vivo. In the present study, we investigated the role of GE on ceramide synthesis in human primary keratinocytes (HPKs) and psoriasis-like keratinocytes. We could demonstrate that GE increased the concentrations of glucosylceramides and the ceramide AS/AdS subclass without affecting the overall ceramide content in HPKs. The expression of ceramide synthase 3 (CERS3) and elongases (ELOVL1 and 4) was reduced in psoriasis lesions compared to healthy skin. Psoriasis-like HPKs, generated by stimulating HPKs with cytokines that are involved in the pathogenesis of psoriasis (IL-17, TNF-α, IL-22 and IFN-γ) showed increased levels of IL-6, IL-8 and increased expression of DEFB4A, as well as decreased expression of ELOVL4. The treatment with GE partly rescued the reduced expression of ELOVL4 in psoriasis-like HPKs and augmented CERS3 expression. This study has shown that GE modulates ceramide synthesis in keratinocytes. Therefore, GE might be a novel topical treatment for skin diseases with an altered lipid composition such as psoriasis.

Zobrazit více v PubMed

Bouwstra J.A., Ponec M. The skin barrier in healthy and diseased state. Biochim. Biophys. Acta. 2006;1758:2080–2095. doi: 10.1016/j.bbamem.2006.06.021. PubMed DOI

Van Smeden J., Janssens M., Gooris G.S., Bouwstra J.A. The important role of stratum corneum lipids for the cutaneous barrier function. Biochim. Biophys. Acta. 2014;1841:295–313. doi: 10.1016/j.bbalip.2013.11.006. PubMed DOI

Feingold K.R., Elias P.M. Role of lipids in the formation and maintenance of the cutaneous permeability barrier. Biochim. Biophys. Acta. 2014;1841:280–294. doi: 10.1016/j.bbalip.2013.11.007. PubMed DOI

Rabionet M., Gorgas K., Sandhoff R. Ceramide synthesis in the epidermis. Biochim. Biophys. Acta. 2014;1841:422–434. doi: 10.1016/j.bbalip.2013.08.011. PubMed DOI

Breiden B., Sandhoff K. The role of sphingolipid metabolism in cutaneous permeabilitybarrier formation. Biochim. Biophys. Acta (BBA) Mol. Cell Biol. Lipids. 2014;1841:441–452. doi: 10.1016/j.bbalip.2013.08.010. PubMed DOI

Arakawa A., Siewert K., Stöhr J., Besgen P., Kim S.-M., Rühl G., Nickel J., Vollmer S., Thomas P., Krebs S., et al. Melanocyte antigen triggers autoimmunity in human psoriasis. J. Exp. Med. 2015;212:2203–2212. doi: 10.1084/jem.20151093. PubMed DOI PMC

Gudjonsson J.E., Ding J., Li X., Nair R.P., Tejasvi T., Qin Z.S., Ghosh D., Aphale A., Gumucio D.L., Voorhees J.J., et al. Global Gene Expression Analysis Reveals Evidence for Decreased Lipid Biosynthesis and Increased Innate Immunity in Uninvolved Psoriatic Skin. J. Investig. Dermatol. 2009;129:2795–2804. doi: 10.1038/jid.2009.173. PubMed DOI PMC

Wolf R., Orion E., Ruocco E., Ruocco V. Abnormal epidermal barrier in the pathogenesis of psoriasis. Clin. Dermatol. 2012;30:323–328. doi: 10.1016/j.clindermatol.2011.08.022. PubMed DOI

Ye L., Lv C., Man G., Song S., Elias P.M., Man M.-Q. Abnormal Epidermal Barrier Recovery in Uninvolved Skin supports the Notion of an Epidermal Pathogenesis of Psoriasis. J. Investig. Derm. 2014;134:2843–2846. doi: 10.1038/jid.2014.205. PubMed DOI PMC

Motta S., Monti M., Sesana S., Caputo R., Carelli S., Ghidoni R. Ceramide composition of the psoriatic scale. Biochim. Biophys. Acta. 1993;1182:147–151. doi: 10.1016/0925-4439(93)90135-N. PubMed DOI

Motta S., Monti M., Sesana S., Mellesi L., Ghidoni R., Caputo R. Abnormality of water barrier function in psoriasis. Role of ceramide fractions. Arch. Derm. 1994;130:452–456. doi: 10.1001/archderm.1994.01690040056007. PubMed DOI

Sano S. Psoriasis as a barrier disease. Dermatol. Sin. 2015;33:64–69. doi: 10.1016/j.dsi.2015.04.010. DOI

Cho Y., Lew B.-L., Seong K., Kim N.-I. An inverse relationship between ceramide synthesis and clinical severity in patients with psoriasis. J. Korean Med. Sci. 2004;19:859–863. doi: 10.3346/jkms.2004.19.6.859. PubMed DOI PMC

Kim B.-K., Keum B.-K., Shon J.C., Liu K.-H., Hong S.-P. Ahn Changes in fatty acid lengths of ceramides toward shorter chain dominance in human psoriasis skin | Morressier. [(accessed on 24 October 2019)]; Available online: https://www.google.com/

Kim B., Shon J., Liu K., Hong S., Ahn S. 122 Changes in fatty acid lengths of ceramides toward shorter chain dominance in human psoriasis skin. J. Investig. Dermatol. 2017;137:S213. doi: 10.1016/j.jid.2017.07.432. DOI

Tawada C., Kanoh H., Nakamura M., Mizutani Y., Fujisawa T., Banno Y., Seishima M. Interferon-γ decreases ceramides with long-chain fatty acids: Possible involvement in atopic dermatitis and psoriasis. J. Investig. Dermatol. 2014;134:712–718. doi: 10.1038/jid.2013.364. PubMed DOI

Feingold K.R. The Adverse Effect of IFN Gamma on Stratum Corneum Structure and Function in Psoriasis and Atopic Dermatitis. J. Investig. Dermatol. 2014;134:597–600. doi: 10.1038/jid.2013.440. PubMed DOI

Elias P.M., Wood L.C., Feingold K.R. Epidermal pathogenesis of inflammatory dermatoses. Am. J. Contact Dermat. 1999;10:119–126. PubMed

Wölfle U., Haarhaus B., Seiwerth J., Cawelius A., Schwabe K., Quirin K.-W., Schempp C.M. The Herbal Bitter Drug Gentiana lutea Modulates Lipid Synthesis in Human Keratinocytes In Vitro and In Vivo. Int. J. Mol. Sci. 2017;18:1814. doi: 10.3390/ijms18081814. PubMed DOI PMC

Mizutani Y., Mitsutake S., Tsuji K., Kihara A., Igarashi Y. Ceramide biosynthesis in keratinocyte and its role in skin function. Biochimie. 2009;91:784–790. doi: 10.1016/j.biochi.2009.04.001. PubMed DOI

Leigh I.M., Navsaria H., Purkis P.E., Mckay I.A., Bowden P.E., Riddle P.N. Keratins (Kl6 and Kl7) as markers of keratinocyte hyperproliferation in psoriasis in vivo and in vitro. Br. J. Dermatol. 1995;133:501–511. doi: 10.1111/j.1365-2133.1995.tb02696.x. PubMed DOI

Jakobsson A., Westerberg R., Jacobsson A. Fatty acid elongases in mammals: Their regulation and roles in metabolism. Prog. Lipid Res. 2006;45:237–249. doi: 10.1016/j.plipres.2006.01.004. PubMed DOI

Rabionet M., van der Spoel A.C., Chuang C.-C., von Tümpling-Radosta B., Litjens M., Bouwmeester D., Hellbusch C.C., Körner C., Wiegandt H., Gorgas K., et al. Male Germ Cells Require Polyenoic Sphingolipids with Complex Glycosylation for Completion of Meiosis A LINK TO CERAMIDE SYNTHASE-3. J. Biol. Chem. 2008;283:13357–13369. doi: 10.1074/jbc.M800870200. PubMed DOI PMC

Vasireddy V., Uchida Y., Salem N., Kim S.Y., Mandal M.N.A., Reddy G.B., Bodepudi R., Alderson N.L., Brown J.C., Hama H., et al. Loss of functional ELOVL4 depletes very long-chain fatty acids (≥C28) and the unique ω-O-acylceramides in skin leading to neonatal death. Hum. Mol. Genet. 2007;16:471–482. doi: 10.1093/hmg/ddl480. PubMed DOI PMC

Jennemann R., Rabionet M., Gorgas K., Epstein S., Dalpke A., Rothermel U., Bayerle A., van der Hoeven F., Imgrund S., Kirsch J., et al. Loss of ceramide synthase 3 causes lethal skin barrier disruption. Hum. Mol. Genet. 2012;21:586–608. doi: 10.1093/hmg/ddr494. PubMed DOI

Kim D., Lee N.R., Park S.-Y., Jun M., Lee K., Kim S., Park C.S., Liu K.-H., Choi E.H. As in Atopic Dermatitis, Nonlesional Skin in Allergic Contact Dermatitis Displays Abnormalities in Barrier Function and Ceramide Content. J. Investig. Dermatol. 2017;137:748–750. doi: 10.1016/j.jid.2016.10.034. PubMed DOI

Amen N., Mathow D., Rabionet M., Sandhoff R., Langbein L., Gretz N., Jäckel C., Gröne H.-J., Jennemann R. Differentiation of epidermal keratinocytes is dependent on glucosylceramide:ceramide processing. Hum. Mol. Genet. 2013;22:4164–4179. doi: 10.1093/hmg/ddt264. PubMed DOI

Alessandrini F., Pfister S., Kremmer E., Gerber J.-K., Ring J., Behrendt H. Alterations of glucosylceramide-beta-glucosidase levels in the skin of patients with psoriasis vulgaris. J. Investig. Dermatol. 2004;123:1030–1036. doi: 10.1111/j.0022-202X.2004.23469.x. PubMed DOI

Sassa T., Ohno Y., Suzuki S., Nomura T., Nishioka C., Kashiwagi T., Hirayama T., Akiyama M., Taguchi R., Shimizu H., et al. Impaired epidermal permeability barrier in mice lacking elovl1, the gene responsible for very-long-chain fatty acid production. Mol. Cell. Biol. 2013;33:2787–2796. doi: 10.1128/MCB.00192-13. PubMed DOI PMC

Hong K.-K., Cho H.-R., Ju W.-C., Cho Y., Kim N.-I. A Study on Altered Expression of Serine Palmitoyltransferase and Ceramidase in Psoriatic Skin Lesion. J. Korean Med. Sci. 2007;22:862–867. doi: 10.3346/jkms.2007.22.5.862. PubMed DOI PMC

Nakajima K., Terao M., Takaishi M., Kataoka S., Goto-Inoue N., Setou M., Horie K., Sakamoto F., Ito M., Azukizawa H., et al. Barrier abnormality due to ceramide deficiency leads to psoriasiform inflammation in a mouse model. J. Investig. Dermatol. 2013;133:2555–2565. doi: 10.1038/jid.2013.199. PubMed DOI

Bonté F., Barré P., Pinguet P., Dusser I., Dumas M., Meybeck A. Simarouba amara extract increases human skin keratinocyte differentiation. J. Ethnopharmacol. 1996;53:65–74. doi: 10.1016/0378-8741(96)01423-7. PubMed DOI

Chon S.-H., Tannahill R., Yao X., Southall M.D., Pappas A. Keratinocyte differentiation and upregulation of ceramide synthesis induced by an oat lipid extract via the activation of PPAR pathways. Exp. Dermatol. 2015;24:290–295. doi: 10.1111/exd.12658. PubMed DOI

Schmuth M., Jiang Y.J., Dubrac S., Elias P.M., Feingold K.R. Thematic Review Series: Skin Lipids. Peroxisome proliferator-activated receptors and liver X receptors in epidermal biology. J. Lipid Res. 2008;49:499–509. doi: 10.1194/jlr.R800001-JLR200. PubMed DOI

Michalik L., Wahli W. Peroxisome proliferator-activated receptors (PPARs) in skin health, repair and disease. Biochim. Biophys. Acta (BBA) Mol. Cell Biol. Lipids. 2007;1771:991–998. doi: 10.1016/j.bbalip.2007.02.004. PubMed DOI

Takeda S., Shimoda H., Takarada T., Imokawa G. Strawberry seed extract and its major component, tiliroside, promote ceramide synthesis in the stratum corneum of human epidermal equivalents. PLoS ONE. 2018;13:e0205061. doi: 10.1371/journal.pone.0205061. PubMed DOI PMC

Calderón C., Rubarth L., Cebo M., Merfort I., Lämmerhofer M. Lipid Atlas of Keratinocytes and Betulin Effects on its Lipidome Profiled by Comprehensive UHPLC–MS/MS with Data Independent Acquisition Using Targeted Data Processing. Proteomics. 2019:1900113. doi: 10.1002/pmic.201900113. PubMed DOI

Rheinwald J.G., Green H. Serial cultivation of strains of human epidermal keratinocytes: The formation of keratinizing colonies from single cells. Cell. 1975;6:331–343. doi: 10.1016/S0092-8674(75)80001-8. PubMed DOI

Schmittgen T.D., Livak K.J. Analyzing real-time PCR data by the comparative C T method. Nat. Protoc. 2008;3:1101–1108. doi: 10.1038/nprot.2008.73. PubMed DOI

Vávrová K., Henkes D., Strüver K., Sochorová M., Školová B., Witting M.Y., Friess W., Schreml S., Meier R.J., Schäfer-Korting M., et al. Filaggrin Deficiency Leads to Impaired Lipid Profile and Altered Acidification Pathways in a 3D Skin Construct. J. Investig. Dermatol. 2014;134:746–753. doi: 10.1038/jid.2013.402. PubMed DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...