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Thyroid hormone enhances nitric oxide mediated bacterial clearance and promotes survival after meningococcal infection

Chen, Yao (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Sjölinder, Mikael (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Wang, Xiao (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
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Altenbacher, Georg (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Hagner, Matthias (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Berglund, Pernilla (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Gao, Yumin (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Lu, Ting (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Jonsson, Ann-Beth (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Sjölinder, Hong (author)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
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 (creator_code:org_t)
2012-07-23
2012
English.
In: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 7:7
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Euthyroid sick syndrome characterized by reduced levels of thyroid hormones (THs) is observed in patients with meningococcal shock. It has been found that the level of THs reflects disease severity and is predictive for mortality. The present study was conducted to investigate the impact of THs on host defense during meningococcal infection. We found that supplementation of thyroxine to mice infected with Neisseria meningitidis enhanced bacterial clearance, attenuated the inflammatory responses and promoted survival. In vitro studies with macrophages revealed that THs enhanced bacteria-cell interaction and intracellular killing of meningococci by stimulating inducible nitric oxide synthase (iNos)-mediated NO production. TH treatment did not activate expression of TH receptors in macrophages. Instead, the observed TH-directed actions were mediated through nongenomic pathways involving the protein kinases PI3K and ERK1/2 and initiated at the membrane receptor integrin alpha v beta 3. Inhibition of nongenomic TH signaling prevented iNos induction, NO production and subsequent intracellular bacterial killing by macrophages. These data demonstrate a beneficial role of THs in macrophage-mediated N. meningitidis clearance. TH replacement might be a novel option to control meningococcal septicemia.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Keyword

molekylärgenetik
Molecular Genetics

Publication and Content Type

ref (subject category)
art (subject category)

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