Regulation of Toll-like receptor 1 and -2 in neonatal mice brains after hypoxia-ischemia
2011

Regulation of Toll-like receptors in neonatal mice brains after hypoxia-ischemia

Sample size: 15 publication Evidence: moderate

Author Information

Author(s): Linnea Stridh, Peter LP Smith, Andrew S Naylor, Xiaoyang Wang, Carina Mallard

Primary Institution: Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg

Hypothesis

The expression of Toll-like receptors (TLRs) in the neonatal brain and their regulation after hypoxia-ischemia is unknown.

Conclusion

TLR-2 deficiency reduced hypoxic-ischemic injury in neonatal mice, suggesting it plays a role in neonatal brain injury.

Supporting Evidence

  • TLR-1 was down-regulated at 30 min and up-regulated at 6 h and 24 h after hypoxia-ischemia.
  • TLR-2 was constitutively expressed in astrocytes and a population of neurons in the hypothalamus.
  • TLR-2 KO mice showed a decreased infarct volume compared to wild type after hypoxia-ischemia.

Takeaway

This study found that certain receptors in the brain, called TLRs, change after a lack of oxygen in newborn mice, and one of them, TLR-2, helps protect the brain from damage.

Methodology

Neonatal mice were subjected to hypoxia-ischemia, and TLR mRNA expression was analyzed using RT-qPCR and immunohistochemistry.

Participant Demographics

Neonatal C57BL/6 mice, including wild type and TLR knockout strains.

Statistical Information

P-Value

0.0051

Statistical Significance

p = 0.0051

Digital Object Identifier (DOI)

10.1186/1742-2094-8-45

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