Expression of the Vanin Gene Family in Normal and Inflamed Human Skin: Induction by Proinflammatory Cytokines

被引:69
作者
Jansen, Patrick A. M. [1 ,2 ]
Kamsteeg, Marijke [1 ,2 ]
Rodijk-Olthuis, Diana [1 ,2 ]
van Vlijmen-Willems, Ivonne M. J. J. [1 ,2 ]
de Jongh, Gys J. [1 ,2 ]
Bergers, Mieke [1 ,2 ]
Tjabringa, Geuranne S. [1 ,2 ]
Zeeuwen, Patrick L. J. M. [1 ,2 ]
Schalkwijk, Joost [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Dermatol, NL-6525 ED Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, NL-6525 ED Nijmegen, Netherlands
关键词
ACTIVATED-RECEPTOR-GAMMA; HUMAN EPIDERMAL-KERATINOCYTES; ATOPIC-DERMATITIS; TRANSGLUTAMINASE ACTIVITY; PSORIATIC SKIN; DIFFERENTIATION; PANTETHEINASE; DISEASE; MOUSE; LOCALIZATION;
D O I
10.1038/jid.2009.67
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The vanin gene family encodes secreted and membrane-bound ectoenzymes that convert pantetheine into pantothenic acid and cysteamine. Recent studies in a mouse colitis model indicated that vanin-1 has proinflammatory activity and suggest that pantetheinases are potential therapeutic targets in inflammatory diseases. In a microarray analysis of epidermal gene expression of psoriasis and atopic dermatitis lesions, we identified vanin-3 as the gene showing the highest differential expression of all annotated genes that we studied (19-fold upregulation in psoriasis). Quantitative real-time PCR analysis confirmed the microarray data on vanin-3 and showed similar induction of vanin-1, but not of vanin-2, in psoriatic epidermis. Immunohistochemistry showed that vanin-3 is expressed in the differentiated epidermal layers. Using submerged and organotypic keratinocyte cultures, we found that vanin-1 and vanin-3 are induced at the mRNA and protein level by psoriasis-associated proinflammatory cytokines (Th17/Th1) but not by Th2 cytokines. We hypothesize that increased levels of pantetheinase activity are part of the inflammatory-regenerative epidermal differentiation program, and may contribute to the phenotype observed in psoriasis.
引用
收藏
页码:2167 / 2174
页数:8
相关论文
共 51 条
[11]   INCREASED MEMBRANE-ASSOCIATED TRANSGLUTAMINASE ACTIVITY IN PSORIASIS [J].
ESMANN, J ;
VOORHEES, JJ ;
FISHER, GJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 164 (01) :219-224
[12]   Two human genes related to murine Vanin-1 are located on the long arm of human chromosome 6 [J].
Galland, F ;
Malergue, F ;
Bazin, H ;
Mattei, MG ;
Aurrand-Lions, M ;
Theillet, C ;
Naquet, P .
GENOMICS, 1998, 53 (02) :203-213
[13]   An ESTs description of the new Vanin gene family conserved from fly to human [J].
Granjeaud, S ;
Naquet, P ;
Galland, F .
IMMUNOGENETICS, 1999, 49 (11-12) :964-972
[14]   SKIN WATER LOSS AND ACCIDENTAL HYPOTHERMIA IN PSORIASIS ICHTHYOSIS AND ERYTHRODERMA [J].
GRICE, KA ;
BETTLEY, FR .
BRITISH MEDICAL JOURNAL, 1967, 4 (5573) :195-&
[15]   Transglutaminase inhibitors induce hyperproliferation and parakeratosis in tissue-engineered skin [J].
Harrison, C. A. ;
Layton, C. M. ;
Hau, Z. ;
Bullock, A. J. ;
Johnson, T. S. ;
MacNeil, S. .
BRITISH JOURNAL OF DERMATOLOGY, 2007, 156 (02) :247-257
[16]   Psoriasis is associated with increased β-defensin genomic copy number [J].
Hollox, Edward J. ;
Huffmeier, Ulrike ;
Zeeuwen, Patrick L. J. M. ;
Palla, Raquel ;
Lascorz, Jesús ;
Rodijk-Olthuis, Diana ;
van de Kerkhof, Peter C. M. ;
Traupe, Heiko ;
de Jongh, Gys ;
den Heijer, Martin ;
Reis, Andre ;
Armour, John A. L. ;
Schalkwijk, Joost .
NATURE GENETICS, 2008, 40 (01) :23-25
[17]   Different inhibition characteristics of intracellular transglutaminase activity by cystamine and cysteamine [J].
Jeon, JH ;
Lee, HJ ;
Jang, GY ;
Kim, CW ;
Shin, DM ;
Cho, SY ;
Yeo, EJ ;
Park, SC ;
Kim, IG .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2004, 36 (06) :576-581
[18]   Increased expression of carbonic anhydrase II (CA II) in lesional skin of atopic dermatitis: Regulation by Th2 cytokines [J].
Kamsteeg, Marijke ;
Zeeuwen, Patrick L. J. M. ;
de Jongh, Gys J. ;
Rodijk-Olthuis, Diana ;
Zeeuwen-Franssen, Manon E. J. ;
van Erp, Piet E. J. ;
Schalkwijk, Joost .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 (07) :1786-1789
[19]  
KIM IG, 1993, J BIOL CHEM, V268, P12682
[20]  
Le M, 1996, ARCH DERMATOL RES, V288, P684, DOI 10.1007/BF02505278