Aktuelle Dermatologie 2016; 42(01/02): 20-22
DOI: 10.1055/s-0041-109824
Eine Klinik im Blickpunkt
© Georg Thieme Verlag KG Stuttgart · New York

Antimikrobielle Peptid (AMP)-Forschung an der Kieler Universitäts-Hautklinik

Ein zeitlicher Abriss und Zusammenfassung anlässlich der Pensionierung von Prof. Dr. Jens-Michael SchröderAntimicrobial Peptide (AMP) Research at the Department of Dermatology, University of KielA Historical Review in Celebration of the Retirement of Prof. Dr. Jens-Michael Schröder
J. Harder
Universitäts-Hautklinik Kiel
› Author Affiliations
Further Information

Publication History

Publication Date:
04 February 2016 (online)

Zusammenfassung

Antimikrobielle Peptide (AMPs) sind kleine körpereigene Proteine mit potenter antimikrobieller und auch immunmodulatorischer Aktivität. Eine Fehlregulation von AMPs wird in Verbindung mit diversen infektiösen und entzündlichen Krankheitsgeschehen gebracht. Die AMP-Forschung an der Kieler Universitäts-Hautklinik wurde Mitte der neunziger Jahre initiiert und vorangetrieben von Prof. Dr. rer. nat. Jens-Michael Schröder, der im Jahre 2015 pensioniert wurde. Im Laufe der Jahre konnten diverse neue AMPs entdeckt und charakterisiert werden sowie deren wichtige Rolle in der epithelialen Abwehr aufgedeckt werden, wodurch sich Kiel zu einem international renommierten AMP-Forschungsstandort etablieren konnte.

Abstract

Antimicrobial peptides (AMPs) are small endogeneous proteins exhibiting potent antimicrobial activity as well as immunomodulatory activites. A dysregulation of AMPs may be associated with several infectious and inflammatory diseases. AMP research at the Department of Dermatology in Kiel started in the mid 1990s and was initiated and driven by Prof. Dr. rer. nat. Jens-Michael Schröder who retired in 2015. Over the years the discovery and characterization of diverse novel AMPs as well as uncovering their important role in epithelial defense established Kiel as an international renowned AMP research site.

 
  • Literatur

  • 1 Zasloff M. Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor. Proc Natl Acad Sci USA 1987; 84: 5449-5453
  • 2 Harder J, Schröder JM. Psoriatic scales: a promising source for the isolation of human skin-derived antimicrobial proteins. J Leukoc Biol 2005; 77: 476-486
  • 3 Henseler T, Christophers E. Disease concomitance in psoriasis. J Am Acad Dermatol 1995; 32: 982-986
  • 4 Harder J, Bartels J, Christophers E et al. A peptide antibiotic from human skin. Nature 1997; 387: 861
  • 5 Harder J, Bartels J, Christophers E et al. Isolation and characterization of human beta-defensin-3, a novel human inducible peptide antibiotic. J Biol Chem 2001; 27: 5707-5713
  • 6 Gläser R, Meyer-Hoffert U, Harder J et al. The antimicrobial protein psoriasin (S100A7) is upregulated in atopic dermatitis and after experimental skin barrier disruption. J Invest Dermatol 2009; 129: 641-649
  • 7 Harder J, Dressel S, Wittersheim M et al. Enhanced expression and secretion of antimicrobial peptides in atopic dermatitis and after superficial skin injury. J Invest Dermatol 2010; 130: 1355-1364
  • 8 Harder J, Schröder JM. Antimicrobial peptides in human skin. Chem Immunol Allergy 2005; 86: 22-41
  • 9 Gläser R, Harder J, Lange H et al. Antimicrobial psoriasin (S100A7) protects human skin from Escherichia coli infection. Nat Immunol 2005; 6: 57-64
  • 10 Harder J, Schröder JM. RNase 7, a novel innate immune defense antimicrobial protein of healthy human skin. J Biol Chem 2002; 277: 46779-46784
  • 11 Firat YH, Simanski M, Rademacher F et al. Infection of Keratinocytes with Trichophytum rubrum Induces Epidermal Growth Factor-Dependent RNase 7 and Human Beta-Defensin-3 Expression. PLoS One 2014; 9: e93941
  • 12 Fritz P, Beck-Jendroschek V, Brasch J. Inhibition of dermatophytes by the antimicrobial peptides human beta-defensin-2, ribonuclease 7 and psoriasin. Medical mycology 2012; 50: 579-584
  • 13 Hein KZ, Takahashi H, Tsumori T et al. Disulphide-reduced psoriasin is a human apoptosis-inducing broad-spectrum fungicide. Proc Natl Acad Sci USA 2015; 112: 13039-13044
  • 14 Hilchie AL, Wuerth K, Hancock RE. Immune modulation by multifaceted cationic host defense (antimicrobial) peptides. Nature chemical biology 2013; 9: 761-768
  • 15 Eilers Jr RE, Gandhi M, Patel JD et al. Dermatologic infections in cancer patients treated with epidermal growth factor receptor inhibitor therapy. Journal of the National Cancer Institute 2010; 102: 47-53
  • 16 Kopfnagel V, Harder J, Werfel T. Expression of antimicrobial peptides in atopic dermatitis and possible immunoregulatory functions. Current opinion in allergy and clinical immunology 2013; 13: 531-536
  • 17 Lichtenberger BM, Gerber PA, Holcmann M et al. Epidermal EGFR controls cutaneous host defense and prevents inflammation. Sci Transl Med 2013; 5: 199ra111
  • 18 Minegishi Y, Saito M, Nagasawa M et al. Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome. J Exp Med 2009; 206: 1291-1301
  • 19 Schröder JM. Antimicrobial peptides in healthy skin and atopic dermatitis. Allergol Int 2011; 60: 17-24
  • 20 Ostaff MJ, Stange EF, Wehkamp J. Antimicrobial peptides and gut microbiota in homeostasis and pathology. EMBO molecular medicine 2013; 5: 1465-1483
  • 21 Spencer JD, Schwaderer AL, Dirosario JD et al. Ribonuclease 7 is a potent antimicrobial peptide within the human urinary tract. Kidney Int 2011; 80: 174-180
  • 22 Zasloff M. Antimicrobial peptides, innate immunity, and the normally sterile urinary tract. JASN 2007; 18: 2810-2816
  • 23 Bracke S, Carretero M, Guerrero-Aspizua S et al. Targeted silencing of DEFB4 in a bioengineered skin-humanized mouse model for psoriasis: development of siRNA SECosome-based novel therapies. Exp Dermatol 2014; 23: 199-201
  • 24 Hollox EJ, Huffmeier U, Zeeuwen PL et al. Psoriasis is associated with increased beta-defensin genomic copy number. Nat Genet 2008; 40: 23-25
  • 25 Dorschner RA, Williams MR, Gallo RL. Rosacea, the face of innate immunity. Br J Dermatol 2014; 171: 1282-1284
  • 26 Gallo RL, Nakatsuji T. Microbial symbiosis with the innate immune defense system of the skin. J Invest Dermatol 2011; 131: 1974-1980
  • 27 Harder J, Schröder JM, Gläser R. The skin surface as antimicrobial barrier: present concepts and future outlooks. Exp Dermatol 2013; 22: 1-5
  • 28 Gläser R, Navid F, Schuller W et al. UV-B radiation induces the expression of antimicrobial peptides in human keratinocytes in vitro and in vivo. J Allergy Clin Immunol 2009; 123: 1117-1123