Absence of TLR4 Reduces Neurovascular Unit and Secondary Inflammatory Process after Traumatic Brain Injury in Mice

Akbar Ahmad, Rosalia Crupi, Michela Campolo, Tiziana Genovese, Emanuela Esposito, Salvatore Cuzzocrea

Research output: Contribution to journalArticle

60 Citations (Scopus)

Abstract

Background: Traumatic brain injury (TBI) initiates a neuroinflammatory cascade that contributes to neuronal damage and behavioral impairment. Toll-like receptors (TLRs) are signaling receptors in the innate immune system, although emerging evidence indicates their role in brain injury. We have therefore investigated the role played by TLR4 signaling pathway in the development of mechanisms of secondary inflammatory process in traumatic brain injury (TBI) differ in mice that lack a functional TLR4 signaling pathway. Methods/Principal Findings: Controlled cortical impact injury was performed on TLR4 knockout (KO) mice (C57BL/10ScNJ) and wild-type (WT) mice (C57BL/10ScNJ). TBI outcome was evaluated by determination of infarct volume and assessment of neurological scores. Brains were collected at 24 h after TBI. When compared to WT mice, TLR4 KO mice had lower infarct volumes and better outcomes in neurological and behavioral tests (evaluated by EBST and rotarod test). Mice that lacked TLR4 had minor expression of TBI-induced GFAP, Chymase, Tryptase, IL-1β, iNOS, PARP and Nitrotyrosine mediators implicated in brain damage. The translocation of expression of p-JNK, IκB-α and NF-κB pathway were also lower in brains from TLR4 KO mice. When compared to WT mice, resulted in significant augmentation of all the above described parameters. In addition, apoptosis levels in TLR4 KO mice had minor expression of Bax while on the contrary with Bcl-2. Conclusions/Significance: Our results clearly demonstrated that absence of TLR4 reduces the development of neuroinflammation, tissues injury events associated with brain trauma and may play a neuroprotective role in TBI in mice.

Original languageEnglish (US)
Article numbere57208
JournalPLoS One
Volume8
Issue number3
DOIs
StatePublished - Mar 28 2013
Externally publishedYes

Fingerprint

Brain
brain
Knockout Mice
mice
infarction
Rotarod Performance Test
Chymases
Tryptases
Toll-Like Receptors
Wounds and Injuries
tryptase
Traumatic Brain Injury
Interleukin-1
Inbred C57BL Mouse
Brain Injuries
brain damage
Immune System
interleukin-1
Immune system
Apoptosis

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Absence of TLR4 Reduces Neurovascular Unit and Secondary Inflammatory Process after Traumatic Brain Injury in Mice. / Ahmad, Akbar; Crupi, Rosalia; Campolo, Michela; Genovese, Tiziana; Esposito, Emanuela; Cuzzocrea, Salvatore.

In: PLoS One, Vol. 8, No. 3, e57208, 28.03.2013.

Research output: Contribution to journalArticle

Ahmad, Akbar ; Crupi, Rosalia ; Campolo, Michela ; Genovese, Tiziana ; Esposito, Emanuela ; Cuzzocrea, Salvatore. / Absence of TLR4 Reduces Neurovascular Unit and Secondary Inflammatory Process after Traumatic Brain Injury in Mice. In: PLoS One. 2013 ; Vol. 8, No. 3.
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