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2006 | 58 | 2 |

Tytuł artykułu

Ocena dzialania peptydow antydrobnoustrojowych z hodowli keratynocytow HaCaT na wybrane szczepy bakterii pochodzace ze zmian skornych

Warianty tytułu

EN
The influence of AMPs from HaCaT keratinocytes on some bacteria strains derived from skin changes

Języki publikacji

PL

Abstrakty

PL
Celem badania była ocena działania antydrobnoustrojowego białek pochodzących z ciągłej linii keratynocytów HaCaT na kliniczne izolaty szczepów bakterii Gram-dodatnich. Zbadano wpływ otrzymanego białkowego ekstraktu komórkowego (BEK) na wyżej wymienione szczepy. Zaobserwowano znaczne zróżnicowanie aktywności ekstraktu ze względu na czas inkubacji oraz rodzaj szczepu poddanego działaniu BEK.
EN
The aim of this study was to evaluate antimicrobial activity of protein extracts from HaCaT cell line against bacterial strains, isolated from clinical materials, obtained from patients with clinical symptoms of acne (Propionibacterium acnes) and gas gangrene (Clostridium perfringens and Sterptococcus pyogenes). Reference strain of Staphylococcus aureus ATCC 25923 also was used. Protein extracts from cultured HaCaT cells were obtained by 3-fold freezing/defreezing cells in dry ice following by centrifugation and incubated with appropriate bacterial suspension (0,5 McFarland scale) during 6 and 24 hours. We observed time-depending and strain-depending activity of HaCaT - protein extract. Interestingly, high activity was demonstrated against strains of S. pyogenes and C. perfringens. Because of increasing bacterial resistance to antibiotics further studies in the field of antimicrobial peptides are required.

Wydawca

-

Rocznik

Tom

58

Numer

2

Opis fizyczny

s.163-168,tab.,bibliogr.

Twórcy

autor
  • Slaska Akademia Medyczna w Katowicach, ul.Medykow 18, 40-752 Katowice
autor
autor

Bibliografia

  • 1. Boukamp P, Petrussevska RT, Breitkreutz D i inni. Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line. J Cell Biol. 1988; 106: 761-71.
  • 2. Braff MH, Bardan A, Nizet V i inni. Cutaneous defense mechanisms by antimicrobial peptides. J Invest Dermatol. 2005;125: 9-13.
  • 3. Chen X, Niyonsaba F, Ushio H i inni. Synergistic effect of antibacterial agents human beta-defensins, cathelicidin LL-37 and lysozyme against Staphylococcus aureus and Escherichia coli. J Dermatol Sci. 2005; 40: 123-32.
  • 4. Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanatephenol-chloroform extraction. Anal Biochem. 1987; 162: 156-9.
  • 5. Dartois V, Sanchez-Quesada J, Cabezas E i inni. Systemic antibacterial activity of novel synthetic cyclic peptides. Antimicrob Agents Chemother. 2005; 49: 3302-10.
  • 6. Dinulos JG, Mentele L, Fredericks LP i inni. Keratinocyte expression of human beta defensin 2 following bacterial infection: role in cutaneous host defense. Clin Diagn Lab Immunol. 2003; 10: 161-6.
  • 7. Dorschner RA, Pesionjamasp VK, Tamakuwala S i inni. Cutaneous injury induces the release of cathelicidin anti-microbial peptides active against group A Streptococcus. J Invest Dermatol. 2001; 117: 91-7.
  • 8. Edwards ML, Fagan PK, Smith-Vaughan H i inni. Strains of Streptococcus pyogenes from severe invasive infections bind HEp2 and HaCaT cells more avidly than strains from uncomplicated infections. J Clin Microbiol. 2003; 41: 3936-8.
  • 9. Frohm M, Gunne H, Bergman AC i inni. Biochemical and antibacterial analysis of human wound and blister fluid. Eur J Biochem. 1996; 237: 86-92.
  • 10. Harder J, Bartels J, Christophers E i inni. Isolation and characterization of human beta-defensin-3, a novel human inducible peptide antibiotic. J Biol Chem. 2001; 276: 5707-13.
  • 11. Koczulla AR, Bals R. Antimicrobial peptides: current status and therapeutic potential. Drugs. 2003; 63: 389-406.
  • 12. Lee PH, Ohtake T, Zaiou M i inni. Expression of an additional cathelicidin antimicrobial peptide protects against bacterial skin infection. Proc Natl Acad Sci USA. 2005; 102: 3750-5.
  • 13. Mempel M, Schmidt T, Weidinger S i inni. Role of Staphylococcus aureus surface-associated proteins in the attachment to cultured HaCaT keratinocytes in a new adhesion assay. J Invest Dermatol. 1998; 111:452-6.
  • 14. Midorsikawa K, Ouhara K, Komatsuzawa H i inni. Staphylococcus aureus susceptibility to innate antimicrobial peptides, beta-defensins and CAP 18, expressed by human keratinocytes. Infect Immun. 2003;71:3730-9.
  • 15. Murakami M, Ohtake T, Dorschner RA i inni. Cathelicidin anti-microbial peptide expression in sweat, an innate defense system for the skin. J Invest Dermatol. 2002; 119: 1090-5.
  • 16. Nagy I, Pivarcsi A, Koreck A i inni. Distinct strains of Propionibacterium acnes induce selective human beta-defensin-2 and interleukin-8 expression in human keratinocytes through toll-like receptors. J Invest Dermatol. 2005; 124: 931-8.
  • 17. Sayama K, Komatsuzawa H, Yamasaki K i inni. New mechanisms of skin innate immunity: ASK1- mediated keratinocyte differentiation regulates the expression of beta-defensins, LL37, and TLR2. Eur J Immunol. 2005; 35: 1886-95.
  • 18. Seo SJ, Ahn SW, Hong CK i inni. Expressions of beta-defensins in human keratinocyte cell lines. J Dermatol Sci. 2001; 27: 183-91.
  • 19. Sorensen OE, Thapa DR, Rosenthal A i inni. Differential regulation of beta-defensin expression in human skin by microbial stimuli. J Immunol. 2005; 174: 4870-9.
  • 20. Weidenmaier C, Kristian SA, Peschel A. Bacterial resistance to antimicrobial host defenses-an emerging target for novel antiinfective strategies? Curr Drug Targets. 2003; 4: 643-9.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-9750747e-42c2-41c9-8d22-dd55534e3524
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