FEMS Immunology and Medical Microbiology 2005-08-01

Determination of the cytotoxic effect of Clostridium histolyticum culture supernatant on HeLa cells in the presence of protease inhibitors.

Jarosław Jóźwiak, Aldona Komar, Ewa Jankowska, Gayane Martirosian

文献索引:FEMS Immunol. Med. Microbiol. 45(2) , 137-42, (2005)

全文:HTML全文

摘要

Clostridium histolyticum culture supernatant contains numerous enzymes, which exert a cytotoxic effect on host cells. This includes lethal toxin, clostripain and high-potassium-sensitive toxin. Since the number of C. histolyticum infections increased during the last several years, it seems worthwhile to evaluate whether protease inhibitors, used for the treatment of many diseases, could influence toxicity, and thus, pathogenicity of C. histolyticum. In this study we evaluated in vitro the influence of four common protease inhibitors: aprotinin, phenylmethylsulphonyl fluoride (PMSF), l-1-chloro-3-[4-tosylamido]-7-amino-2-heptanone-HCl (TLCK) and chymostatin on the toxicity of C. histolyticum supernatant towards human epithelial HeLa cells. We show that aprotinin has no effect, while PMSF, TLCK and chymostatin potentiate the cytotoxic activity of C. histolyticum, probably by hindering natural defence mechanisms of cells. In addition, PMSF and TLCK block clostripain enzymatic activity, while chymostatin leaves it intact. Elevated cytotoxicity of the supernatant is not related to the quantity of high-potassium-sensitive toxin, as was reported previously, since desalted supernatant still exerted its strong toxic effect. Our results show that addition of protease inhibitors for treating diseases complicated by concurrent C. histolyticum infection must require special attention.


相关化合物

  • 胰凝乳蛋白酶抑制剂
  • 梭菌蛋白酶 来源于...
  • 对甲苯磺酰气氟

相关文献:

Enabling Low Cost Biopharmaceuticals: A Systematic Approach to Delete Proteases from a Well-Known Protein Production Host Trichoderma reesei.

2015-01-01

[PLoS ONE 10 , e0134723, (2015)]

Estrogen inhibits mast cell chymase release to prevent pressure overload-induced adverse cardiac remodeling.

2015-02-01

[Hypertension 65(2) , 328-34, (2015)]

Primacy of angiotensin converting enzyme in angiotensin-(1-12) metabolism.

2013-09-01

[Am. J. Physiol. Heart Circ. Physiol. 305(5) , H644-50, (2013)]

Contractility of placental vascular smooth muscle cells in response to stimuli produced by the placenta: roles of ACE vs. non-ACE and AT1 vs. AT2 in placental vessel cells.

2008-06-01

[Placenta 29(6) , 503-9, (2008)]

The structure of chymostatin, a chymotrypsin inhibitor.

1973-11-01

[J. Antibiot. 26(11) , 625-46, (1973)]

更多文献...