Serine proteinase inhibitors in the skin:: Role in homeostasis and disease

被引:15
作者
Mägert, HJ
Drögemüller, K
Raghunath, M
机构
[1] Anhalt Univ Appl Sci, Fac 7, Kothen, Germany
[2] IPF PharmaCeut GmbH, Hannover, Germany
[3] Natl Univ Singapore, Fac Engn, Dept Bioengn, Singapore 117548, Singapore
[4] Natl Univ Singapore, Fac Med, Dept Biochem, Singapore 117548, Singapore
关键词
Netherton syndrome; atopic dermatitis; psoriasis; LEKTI; SPINK5; kallikreins; keratinocytes;
D O I
10.2174/1389203054065374
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Serine proteinases fulfill and facilitate a broad spectrum of biological processes. They are held in check by different specific inhibitors. This delicate balance can be disturbed by genetic defects or exogenous influences and has been shown as the underlying or promoting cause for a large number of different diseases. For instance, proteinases are under investigation as drug targets for cancer, infections, neurodegenerative diseases, osteoporosis, inflammatory disorders and many more. Dermatological research has contributed greatly to the appreciation of the complex regulatory network between serine proteinases and serine proteinase inhibitors. In addition, proteolytically trimmed proteinase-activated receptors (PARs) trigger keratinocyte proliferation and differentiation as well as leukocyte attraction and activation. New insights have been gained particularly concerning the progression of inflammatory disorders of the skin. This review summarizes the role of serine proteinase inhibitors in physiology and pathophysiology of the skin.
引用
收藏
页码:241 / 254
页数:14
相关论文
共 174 条
[1]   Cloning and characterization of hurpin (protease inhibitor 13):: A new skin-specific, UV-repressible serine proteinase inhibitor of the ovalbumin serpin family [J].
Abts, HF ;
Welss, T ;
Mirmohammadsadegh, A ;
Köhrer, K ;
Michel, G ;
Ruzicka, T .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 293 (01) :29-39
[2]   Analysis of UVB-modulated gene expression in human keratinocytes by mRNA differential display polymerase chain reaction [J].
Abts, HF ;
Breuhahn, K ;
Michel, G ;
Kohrer, K ;
Esser, P ;
Ruzicka, T .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (03) :363-367
[3]   Purification and partial amino acid sequence of proteins from human epidermal keratinocyte conditioned medium [J].
Ahmed, A ;
Kandola, P ;
Ziada, G ;
Parenteau, N .
JOURNAL OF PROTEIN CHEMISTRY, 2001, 20 (04) :273-278
[4]   Atopic dermatitis [J].
Ahuja, A ;
Land, K ;
Barnes, CJ .
SOUTHERN MEDICAL JOURNAL, 2003, 96 (11) :1068-1072
[5]  
AKES IA, 2000, AM J PHYSIOL-LUNG C, V278, pL193
[6]   ELASTASE INHIBITION BY THE INTER-ALPHA-TRYPSIN INHIBITOR AND DERIVED INHIBITORS OF MAN AND CATTLE [J].
ALBRECHT, GJ ;
HOCHSTRASSER, K ;
SALIER, JP .
HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1983, 364 (12) :1703-1708
[7]   Distribution and potential biologic function of the thrombin receptor PAR-1 on human keratinocytes [J].
Algermissen, B ;
Sitzmann, J ;
Nürnberg, W ;
Laubscher, JC ;
Henz, BM ;
Bauer, F .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 2000, 292 (10) :488-495
[8]   LEVELS OF SKIN-DERIVED ANTILEUKOPROTEINASE (SKALP) ELAFIN IN SERUM CORRELATE WITH DISEASE-ACTIVITY DURING TREATMENT OF SEVERE PSORIASIS WITH CYCLOSPORINE-A [J].
ALKEMADE, HAC ;
DEJONGH, GJ ;
ARNOLD, WP ;
VANDEKERKHOF, PCM ;
SCHALKWIJK, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (02) :189-193
[9]  
ALKEMADE HAC, 1993, AM J PATHOL, V143, P1679
[10]  
ALKEMADE JAC, 1994, J CELL SCI, V107, P2335