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Erschienen in: Archives of Dermatological Research 6/2018

04.05.2018 | Concise Communication

Up-regulation of HMGB1 and TLR4 in skin lesions of lichen planus

verfasst von: Gabriel Costa de Carvalho, Fabiana Yasumoto Araujo Hirata, Rosana Domingues, Cristina Adelaide Figueiredo, Mariana Colombini Zaniboni, Naiura Vieira Pereira, Mirian Nacagami Sotto, Valéria Aoki, Alberto José da Silva Duarte, Maria Notomi Sato

Erschienen in: Archives of Dermatological Research | Ausgabe 6/2018

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Abstract

Lichen planus (LP) is a chronic, mucocutaneous inflammatory disease of an unknown aetiology. The disease has been associated with certain viruses, and the factors such as DAMPs (damage-associated molecular patterns) and PAMPs (pathogen-associated molecular patterns) may also contribute to the inflammatory response in LP. HMGB1 (high mobility group box 1 protein) is one of the major DAMPs that induces inflammation and could trigger LP disease. The present study was aimed to examine TLR4, RAGE and HMGB1 production in epidermis or dermis by immunohistochemistry and the respective expression of these targets in the skin lesions of patients with LP. Moreover, we measured HMGB1 serum levels by ELISA. The results showed similar profile of expression by HMGB1 and TLR4, which are decreased at epidermis and up-regulated at dermis of skin lesions of LP patients that was sustained by intense cellular infiltration. RAGE expression was also increased in dermis of LP. Although there is increased RAGE protein levels, a decreased RAGE transcript levels was detected. Similar HMGB1 serum levels were detected in the LP and control groups. This study demonstrates that HMGB1 and TLR4 could contribute to the inflammatory LP process in skin.
Literatur
1.
Zurück zum Zitat Abdulahad DA, Westra J, Bijzet J, Limburg PC, Kallenberg CG, Bijl M (2011) High mobility group box 1 (HMGB1) and anti-HMGB1 antibodies and their relation to disease characteristics in systemic lupus erythematosus. Arthritis Res Ther 13(3):R71CrossRefPubMedPubMedCentral Abdulahad DA, Westra J, Bijzet J, Limburg PC, Kallenberg CG, Bijl M (2011) High mobility group box 1 (HMGB1) and anti-HMGB1 antibodies and their relation to disease characteristics in systemic lupus erythematosus. Arthritis Res Ther 13(3):R71CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Andersson U, Wang H, Palmblad K, Aveberger AC, Bloom O, Erlandsson-Harris H, Tracey KJ (2000) High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes. J Exp Med 192(4):565–570CrossRefPubMedPubMedCentral Andersson U, Wang H, Palmblad K, Aveberger AC, Bloom O, Erlandsson-Harris H, Tracey KJ (2000) High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes. J Exp Med 192(4):565–570CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat Barkauskaite V, Ek M, Popovic K, Harris HE, Wahren-Herlenius M, Nyberg F (2007) Translocation of the novel cytokine HMGB1 to the cytoplasm and extracellular space coincides with the peak of clinical activity in experimentally UV-induced lesions of cutaneous lupus erythematosus. Lupus 16(10):794–802CrossRefPubMed Barkauskaite V, Ek M, Popovic K, Harris HE, Wahren-Herlenius M, Nyberg F (2007) Translocation of the novel cytokine HMGB1 to the cytoplasm and extracellular space coincides with the peak of clinical activity in experimentally UV-induced lesions of cutaneous lupus erythematosus. Lupus 16(10):794–802CrossRefPubMed
4.
Zurück zum Zitat Bartling B, Hofmann HS, Weigle B, Silber RE, Simm A (2005) Down-regulation of the receptor for advanced glycation end-products (RAGE) supports non-small cell lung carcinoma. Carcinogenesis 26(2):293–301CrossRefPubMed Bartling B, Hofmann HS, Weigle B, Silber RE, Simm A (2005) Down-regulation of the receptor for advanced glycation end-products (RAGE) supports non-small cell lung carcinoma. Carcinogenesis 26(2):293–301CrossRefPubMed
5.
Zurück zum Zitat Bergmann C, Strohbuecker L, Lotfi R, Sucker A, Joosten I, Koenen H, Körber A (2016) High mobility group box 1 is increased in the sera of psoriatic patients with disease progression. J Eur Acad Dermatol Venereol 30(3):435–441CrossRefPubMed Bergmann C, Strohbuecker L, Lotfi R, Sucker A, Joosten I, Koenen H, Körber A (2016) High mobility group box 1 is increased in the sera of psoriatic patients with disease progression. J Eur Acad Dermatol Venereol 30(3):435–441CrossRefPubMed
6.
Zurück zum Zitat Bonaldi T, Talamo F, Scaffidi P, Ferrera D, Porto A, Bachi A, Bianchi ME (2003) Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion. The EMBO journal 22(20):5551–5560CrossRefPubMedPubMedCentral Bonaldi T, Talamo F, Scaffidi P, Ferrera D, Porto A, Bachi A, Bianchi ME (2003) Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion. The EMBO journal 22(20):5551–5560CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Chen T, Guo ZP, Li L, Wang L, Jia RZ, Cao N, Li MM (2013) Increased HMGB1 serum levels and altered HMGB1 expression in patients with psoriasis vulgaris. Arch Dermatol Res 305(3):263–267CrossRefPubMed Chen T, Guo ZP, Li L, Wang L, Jia RZ, Cao N, Li MM (2013) Increased HMGB1 serum levels and altered HMGB1 expression in patients with psoriasis vulgaris. Arch Dermatol Res 305(3):263–267CrossRefPubMed
9.
Zurück zum Zitat de Carvalho GC, Domingues R, de Sousa Nogueira MA, Calvielli Castelo Branco AC, Gomes Manfrere KC, Pereira NV, Aoki V, Sotto MN, Da Silva Duarte AJ, Sato MN (2016) Up-regulation of Proinflammatory Genes and Cytokines Induced by S100A8 in CD8 + T Cells in Lichen Planus. Acta dermato-venereologica 96(4):485–489. https://doi.org/10.2340/00015555-2306 CrossRefPubMed de Carvalho GC, Domingues R, de Sousa Nogueira MA, Calvielli Castelo Branco AC, Gomes Manfrere KC, Pereira NV, Aoki V, Sotto MN, Da Silva Duarte AJ, Sato MN (2016) Up-regulation of Proinflammatory Genes and Cytokines Induced by S100A8 in CD8 + T Cells in Lichen Planus. Acta dermato-venereologica 96(4):485–489. https://​doi.​org/​10.​2340/​00015555-2306 CrossRefPubMed
10.
Zurück zum Zitat De Vries HJ, van Marle J, Teunissen MB, Picavet D, Zorgdrager F, Bos JD (2006) Lichen planus is associated with human herpesvirus type 7 replication and infiltration of plasmacytoid dendritic cells. Br J Dermatol 154(2):361–364CrossRefPubMed De Vries HJ, van Marle J, Teunissen MB, Picavet D, Zorgdrager F, Bos JD (2006) Lichen planus is associated with human herpesvirus type 7 replication and infiltration of plasmacytoid dendritic cells. Br J Dermatol 154(2):361–364CrossRefPubMed
11.
Zurück zum Zitat Domingues R, de Carvalho GC, da Silva Oliveira LM, Futata Taniguchi E, Zimbres JM, Aoki V, da Silva Duarte AJ, Sato MN (2015) The dysfunctional innate immune response triggered by toll-like receptor activation is restored by TLR7/TLR8 and TLR9 ligands in cutaneous lichen planus. Br J Dermatol 172(1):48–55CrossRefPubMed Domingues R, de Carvalho GC, da Silva Oliveira LM, Futata Taniguchi E, Zimbres JM, Aoki V, da Silva Duarte AJ, Sato MN (2015) The dysfunctional innate immune response triggered by toll-like receptor activation is restored by TLR7/TLR8 and TLR9 ligands in cutaneous lichen planus. Br J Dermatol 172(1):48–55CrossRefPubMed
12.
Zurück zum Zitat Einck L, Bustin M (1985) The intracellular distribution and function of the high mobility group chromosomal proteins. Exp Cell Res 156:295–310CrossRefPubMed Einck L, Bustin M (1985) The intracellular distribution and function of the high mobility group chromosomal proteins. Exp Cell Res 156:295–310CrossRefPubMed
13.
Zurück zum Zitat Englert JM, Hanford LE, Kaminski N, Tobolewski JM, Tan RJ, Fattman CL, Kasper M (2008) A role for the receptor for advanced glycation end products in idiopathic pulmonary fibrosis. Am J Pathol 172(3):583–591CrossRefPubMedPubMedCentral Englert JM, Hanford LE, Kaminski N, Tobolewski JM, Tan RJ, Fattman CL, Kasper M (2008) A role for the receptor for advanced glycation end products in idiopathic pulmonary fibrosis. Am J Pathol 172(3):583–591CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Guo HF, Liu SX, Zhang YJ, Liu QJ, Hao J, Gao LX (2011) High mobility group box 1 induces synoviocyte proliferation in rheumatoid arthritis by activating the signal transducer and activator transcription signal pathway. J Clin Exp Med 11(2):65–74CrossRef Guo HF, Liu SX, Zhang YJ, Liu QJ, Hao J, Gao LX (2011) High mobility group box 1 induces synoviocyte proliferation in rheumatoid arthritis by activating the signal transducer and activator transcription signal pathway. J Clin Exp Med 11(2):65–74CrossRef
15.
Zurück zum Zitat Hudson BI, Carter AM, Harja E, Kalea AZ, Arriero M, Yang H, Schmidt AM (2008) Identification, classification, and expression of RAGE gene splice variants. FASEB J 22(5):1572–1580CrossRefPubMed Hudson BI, Carter AM, Harja E, Kalea AZ, Arriero M, Yang H, Schmidt AM (2008) Identification, classification, and expression of RAGE gene splice variants. FASEB J 22(5):1572–1580CrossRefPubMed
16.
Zurück zum Zitat Huttunen HJ, Fages C, Kuja-Panula J, Ridley AJ, Rauvala H (2002) Receptor for advanced glycation end products-binding COOH-terminal motif of amphoterin inhibits invasive migration and metastasis. Can Res 62(16):4805–4811 Huttunen HJ, Fages C, Kuja-Panula J, Ridley AJ, Rauvala H (2002) Receptor for advanced glycation end products-binding COOH-terminal motif of amphoterin inhibits invasive migration and metastasis. Can Res 62(16):4805–4811
17.
Zurück zum Zitat Irvine C, Irvine F, Champion RH (1991) Long-term follow-up of lichenplanus. Acta Dermatol Venereol 71:242–244 Irvine C, Irvine F, Champion RH (1991) Long-term follow-up of lichenplanus. Acta Dermatol Venereol 71:242–244
19.
Zurück zum Zitat Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25(4):402–408CrossRefPubMed Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25(4):402–408CrossRefPubMed
20.
Zurück zum Zitat Lodi G, Giuliani M, Majorana A, Sardella A, Bez C, Demarosi F (2004) Lichen planus and hepatitis C virus: a multicentre study of patients with oral lesions and a systematic review. Br J Dermatol 151(6):1172–1181CrossRefPubMed Lodi G, Giuliani M, Majorana A, Sardella A, Bez C, Demarosi F (2004) Lichen planus and hepatitis C virus: a multicentre study of patients with oral lesions and a systematic review. Br J Dermatol 151(6):1172–1181CrossRefPubMed
21.
Zurück zum Zitat Lotze MT, Tracey KJ (2005) High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal. Nat Rev Immunol 5(4):331–342CrossRefPubMed Lotze MT, Tracey KJ (2005) High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal. Nat Rev Immunol 5(4):331–342CrossRefPubMed
22.
Zurück zum Zitat Nogueira MA, Gavioli CF, Pereira NZ, de Carvalho GC, Domingues R, Aoki V, Sato MN (2015) Human endogenous retrovirus expression is inversely related with the up-regulation of interferon-inducible genes in the skin of patients with lichen planus. Arch Dermatol Res 307(3):259–264CrossRefPubMed Nogueira MA, Gavioli CF, Pereira NZ, de Carvalho GC, Domingues R, Aoki V, Sato MN (2015) Human endogenous retrovirus expression is inversely related with the up-regulation of interferon-inducible genes in the skin of patients with lichen planus. Arch Dermatol Res 307(3):259–264CrossRefPubMed
23.
Zurück zum Zitat Palumbo R, Sampaolesi M, De Marchis F, Tonlorenzi R, Colombetti S, Mondino A, Bianchi ME (2004) Extracellular HMGB1, a signal of tissue damage, induces mesoangioblast migration and proliferation. J Cell Biol 164(3):441–449CrossRefPubMedPubMedCentral Palumbo R, Sampaolesi M, De Marchis F, Tonlorenzi R, Colombetti S, Mondino A, Bianchi ME (2004) Extracellular HMGB1, a signal of tissue damage, induces mesoangioblast migration and proliferation. J Cell Biol 164(3):441–449CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat Popovic K, Ek M, Espinosa A, Padyukov L, Harris HE, Wahren-Herlenius M, Nyberg F (2005) Increased expression of the novel proinflammatory cytokine high mobility group box chromosomal protein 1 in skin lesions of patients with lupus erythematosus. Arthritis Rheum 52(11):3639–3645CrossRefPubMed Popovic K, Ek M, Espinosa A, Padyukov L, Harris HE, Wahren-Herlenius M, Nyberg F (2005) Increased expression of the novel proinflammatory cytokine high mobility group box chromosomal protein 1 in skin lesions of patients with lupus erythematosus. Arthritis Rheum 52(11):3639–3645CrossRefPubMed
25.
Zurück zum Zitat Semino C, Angelini G, Poggi A, Rubartelli A (2005) NK/iDC interaction results in IL-18 secretion by DCs at the synaptic cleft followed by NK cell activation and release of the DC maturation factor HMGB1. Blood 106(2):609–616CrossRefPubMed Semino C, Angelini G, Poggi A, Rubartelli A (2005) NK/iDC interaction results in IL-18 secretion by DCs at the synaptic cleft followed by NK cell activation and release of the DC maturation factor HMGB1. Blood 106(2):609–616CrossRefPubMed
26.
Zurück zum Zitat Taguchi A, Blood DC, del Toro G, Canet A, Lee DC, Qu W, Hofmann MA (2000) Blockade of RAGE–amphoterin signalling suppresses tumour growth and metastases. Nature 405(6784):354–360CrossRefPubMed Taguchi A, Blood DC, del Toro G, Canet A, Lee DC, Qu W, Hofmann MA (2000) Blockade of RAGE–amphoterin signalling suppresses tumour growth and metastases. Nature 405(6784):354–360CrossRefPubMed
27.
Zurück zum Zitat Taniguchi N, Kawahara KI, Yone K, Hashiguchi T, Yamakuchi M, Goto M, Nakajima T (2003) High mobility group box chromosomal protein 1 plays a role in the pathogenesis of rheumatoid arthritis as a novel cytokine. Arthritis Rheum 48(4):971–981CrossRefPubMed Taniguchi N, Kawahara KI, Yone K, Hashiguchi T, Yamakuchi M, Goto M, Nakajima T (2003) High mobility group box chromosomal protein 1 plays a role in the pathogenesis of rheumatoid arthritis as a novel cytokine. Arthritis Rheum 48(4):971–981CrossRefPubMed
28.
Zurück zum Zitat Tateno T, Ueno S, Hiwatashi K, Matsumoto M, Okumura H, Setoyama T, Shinchi H (2009) Expression of receptor for advanced glycation end products (RAGE) is related to prognosis in patients with esophageal squamous cell carcinoma. Ann Surg Oncol 16(2):440–446CrossRefPubMed Tateno T, Ueno S, Hiwatashi K, Matsumoto M, Okumura H, Setoyama T, Shinchi H (2009) Expression of receptor for advanced glycation end products (RAGE) is related to prognosis in patients with esophageal squamous cell carcinoma. Ann Surg Oncol 16(2):440–446CrossRefPubMed
29.
Zurück zum Zitat Wang H, Bloom O, Zhang M, Vishnubhakat JM, Ombrellino M, Che J, Manogue KR (1999) HMGB-1 as a late mediator of endotoxin lethality in mice. Science 285(5425):248–251CrossRefPubMed Wang H, Bloom O, Zhang M, Vishnubhakat JM, Ombrellino M, Che J, Manogue KR (1999) HMGB-1 as a late mediator of endotoxin lethality in mice. Science 285(5425):248–251CrossRefPubMed
30.
Zurück zum Zitat Yan SF, Ramasamy R, Schmidt AM (2009) Receptor for AGE (RAGE) and its ligands—cast into leading roles in diabetes and the inflammatory response. Int J Mol Med 87(3):235–247CrossRef Yan SF, Ramasamy R, Schmidt AM (2009) Receptor for AGE (RAGE) and its ligands—cast into leading roles in diabetes and the inflammatory response. Int J Mol Med 87(3):235–247CrossRef
31.
Zurück zum Zitat Youn JH, Shin JS (2006) Nucleocytoplasmic shuttling of HMGB1 is regulated by phosphorylation that redirects it toward secretion. J Immunol 177(11):7889–7897CrossRefPubMed Youn JH, Shin JS (2006) Nucleocytoplasmic shuttling of HMGB1 is regulated by phosphorylation that redirects it toward secretion. J Immunol 177(11):7889–7897CrossRefPubMed
32.
Zurück zum Zitat Zhang W, Guo S, Li B, Liu L, Ge R, Cao T, Wang H, Gao T, Wang G, Li C (2016) Proinflammatory effect of high-mobility group protein B1 on keratinocytes: an autocrine mechanism underlying psoriasis development. J Pathol 241(3):392–404CrossRefPubMed Zhang W, Guo S, Li B, Liu L, Ge R, Cao T, Wang H, Gao T, Wang G, Li C (2016) Proinflammatory effect of high-mobility group protein B1 on keratinocytes: an autocrine mechanism underlying psoriasis development. J Pathol 241(3):392–404CrossRefPubMed
Metadaten
Titel
Up-regulation of HMGB1 and TLR4 in skin lesions of lichen planus
verfasst von
Gabriel Costa de Carvalho
Fabiana Yasumoto Araujo Hirata
Rosana Domingues
Cristina Adelaide Figueiredo
Mariana Colombini Zaniboni
Naiura Vieira Pereira
Mirian Nacagami Sotto
Valéria Aoki
Alberto José da Silva Duarte
Maria Notomi Sato
Publikationsdatum
04.05.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Archives of Dermatological Research / Ausgabe 6/2018
Print ISSN: 0340-3696
Elektronische ISSN: 1432-069X
DOI
https://doi.org/10.1007/s00403-018-1837-5

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