TLR2 activation inhibits embryonic neural progenitor cell proliferation

Eitan Okun, Kathleen J. Griffioen, Tae Gen Son, Jong Hwan Lee, Nicholas J. Roberts, Mohamed R. Mughal, Emmette Hutchison, Aiwu Cheng, Thiruma V. Arumugam, Justin D. Lathia, Henriette Van Praag, Mark P. Mattson

Research output: Contribution to journalArticlepeer-review

Abstract

Toll-like receptors (TLRs) play essential roles in innate immunity, and increasing evidence indicates that these receptors are expressed in neurons, astrocytes, and microglia in the brain, where they mediate responses to infection, stress, and injury. To address the possibility that TLR2 heterodimer activation could affect progenitor cells in the developing brain, we analyzed the expression of TLR2 throughout mouse cortical development, and assessed the role of TLR2 heterodimer activation in neuronal progenitor cell (NPC) proliferation. TLR2 mRNA and protein was expressed in the cortex in embryonic and early postnatal stages of development, and in cultured cortical NPC. While NPC from TLR2-deficient and wild type embryos had the same proliferative capacity, TLR2 activation by the synthetic bacterial lipopeptides Pam 3CSK4 and FSL1, or low molecular weight hyaluronan, an endogenous ligand for TLR2, inhibited neurosphere formation in vitro. Intracerebral in utero administration of TLR2 ligands resulted in ventricular dysgenesis characterized by increased ventricle size, reduced proliferative area around the ventricles, increased cell density, an increase in phospho-histone 3 cells, and a decrease in BrdU+ cells in the sub-ventricular zone. Our findings indicate that loss of TLR2 does not result in defects in cerebral development. However, TLR2 is expressed and functional in the developing telencephalon from early embryonic stages and infectious agent-related activation of TLR2 inhibits NPC proliferation. TLR2-mediated inhibition of NPC proliferation may therefore be a mechanism by which infection, ischemia, and inflammation adversely affect brain development.

Original languageEnglish (US)
Pages (from-to)462-474
Number of pages13
JournalJournal of Neurochemistry
Volume114
Issue number2
DOIs
StatePublished - Jul 2010
Externally publishedYes

Keywords

  • cerebral cortex
  • neuronal progenitor cells
  • nuclear factor-κB
  • proliferation
  • toll-like receptors

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

Fingerprint Dive into the research topics of 'TLR2 activation inhibits embryonic neural progenitor cell proliferation'. Together they form a unique fingerprint.

Cite this