Human keratinocytes express cellular prion-related protein in vitro and during inflammatory skin diseases

被引:64
作者
Pammer, J
Weninger, W
Tschachler, E
机构
[1] Univ Vienna, Sch Med, Dept Dermatol, Div Immunol Allergy & Infect Dis, A-1090 Vienna, Austria
[2] Univ Vienna, Sch Med, Inst Clin Pathol, A-1090 Vienna, Austria
关键词
D O I
10.1016/S0002-9440(10)65720-3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Prion diseases are transmissible spongiform encephalopathies of humans and animals characterized by the accumulation of a proteinase-resistant isoform of the cellular prion-related protein (PrPc) within the central nervous system. In the present report we demonstrate for the first time the presence of PrPc on squamous epithelia of normal and diseased human skin and show that inflammatory cytokines regulate PrPc expression in cultured human keratinocytes (KCs). By immunohistochemistry, only little expression of PrPc, which was mainly confined to KCs, was detected in normal skin. In contrast, in inflammatory skin diseases including psoriasis and contact dermatitis, PrPc was strongly present on both KCs and infiltrating mononuclear cells. Strong PrPc expression was also observed in squamous cell carcinomas and viral warts whereas basal cell carcinomas were mostly negative. In mucous membranes of the upper digestive tract and the genital region, distinct PrPc expression by basal squamous epithelial cells was a constant feature. In tissue culture, primary KCs constitutively expressed PrPc mRNA and protein. Exposure of these cells to transforming growth factor (TGF)-alpha or interferon (IFN)-gamma led to an increase of PrPc protein expression. The presence of PrPc on epithelial cells of skin and mucous membranes suggests that these cells represent possible first targets for peripheral infection with prions.
引用
收藏
页码:1353 / 1358
页数:6
相关论文
共 29 条
[1]   Prion research: the next frontiers [J].
Aguzzi, A ;
Weissmann, C .
NATURE, 1997, 389 (6653) :795-798
[2]   Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent [J].
Bruce, ME ;
Will, RG ;
Ironside, JW ;
McConnell, I ;
Drummond, D ;
Suttie, A ;
McCardle, L ;
Chree, A ;
Hope, J ;
Birkett, C ;
Cousens, S ;
Fraser, H ;
Bostock, CJ .
NATURE, 1997, 389 (6650) :498-501
[3]   CELLULAR ISOFORM OF THE SCRAPIE AGENT PROTEIN PARTICIPATES IN LYMPHOCYTE-ACTIVATION [J].
CASHMAN, NR ;
LOERTSCHER, R ;
NALBANTOGLU, J ;
SHAW, I ;
KASCSAK, RJ ;
BOLTON, DC ;
BENDHEIM, PE .
CELL, 1990, 61 (01) :185-192
[4]   THE INFLAMMATORY INFILTRATE IN PSORIASIS [J].
CHRISTOPHERS, E ;
MROWIETZ, U .
CLINICS IN DERMATOLOGY, 1995, 13 (02) :131-135
[5]   Hippocampal slices from prion protein null mice: Disrupted Ca2+-activated K+ currents [J].
Colling, SB ;
Collinge, J ;
Jefferys, JGR .
NEUROSCIENCE LETTERS, 1996, 209 (01) :49-52
[6]   Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytes [J].
Diomede, L ;
Sozzani, S ;
Luini, W ;
Algeri, M ;
DeGioia, L ;
Chiesa, R ;
Lievens, PMJ ;
Bugiani, O ;
Forloni, G ;
Tagliavini, F ;
Salmona, M .
BIOCHEMICAL JOURNAL, 1996, 320 :563-570
[7]   OVEREXPRESSION OF TRANSFORMING GROWTH FACTOR-ALPHA IN PSORIATIC EPIDERMIS [J].
ELDER, JT ;
FISHER, GJ ;
LINDQUIST, PB ;
BENNETT, GL ;
PITTELKOW, MR ;
COFFEY, RJ ;
ELLINGSWORTH, L ;
DERYNCK, R ;
VOORHEES, JJ .
SCIENCE, 1989, 243 (4892) :811-814
[8]  
GAJDUSEK CD, 1996, FIELDS VIROLOGY, P2851
[9]   ASPARAGINE-LINKED GLYCOSYLATION OF THE SCRAPIE AND CELLULAR PRION PROTEINS [J].
HARAGUCHI, T ;
FISHER, S ;
OLOFSSON, S ;
ENDO, T ;
GROTH, D ;
TARENTINO, A ;
BORCHELT, DR ;
TEPLOW, D ;
HOOD, L ;
BURLINGAME, A ;
LYCKE, E ;
KOBATA, A ;
PRUSINER, SB .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1989, 274 (01) :1-13
[10]   Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy [J].
Hill, AF ;
Zeidler, M ;
Ironside, J ;
Collinge, J .
LANCET, 1997, 349 (9045) :99-100