Literature DB >> 19840854

Tumour necrosis factor-alpha impairs neuronal differentiation but not proliferation of hippocampal neural precursor cells: Role of Hes1.

Aoife Keohane1, Sinead Ryan, Eimer Maloney, Aideen M Sullivan, Yvonne M Nolan.   

Abstract

Tumour necrosis factor-alpha (TNFalpha) is a pro-inflammatory cytokine, which influences neuronal survival and function yet there is limited information available on its effects on hippocampal neural precursor cells (NPCs). We show that TNFalpha treatment during proliferation had no effect on the percentage of proliferating cells prepared from embryonic rat hippocampal neurosphere cultures, nor did it affect cell fate towards either an astrocytic or neuronal lineage when cells were then allowed to differentiate. However, when cells were differentiated in the presence of TNFalpha, significantly reduced percentages of newly born and post-mitotic neurons, significantly increased percentages of astrocytes and increased expression of TNFalpha receptors, TNF-R1 and TNF-R2, as well as expression of the anti-neurogenic Hes1 gene, were observed. These data indicate that exposure of hippocampal NPCs to TNFalpha when they are undergoing differentiation but not proliferation has a detrimental effect on their neuronal lineage fate, which may be mediated through increased expression of Hes1. Copyright 2009 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 19840854     DOI: 10.1016/j.mcn.2009.10.003

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  48 in total

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Journal:  J Neuroimmune Pharmacol       Date:  2011-07-05       Impact factor: 4.147

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7.  NFκB signaling regulates embryonic and adult neurogenesis.

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8.  Long nonding RNA UCA1 regulates neural stem cell differentiation by controlling miR-1/Hes1 expression.

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9.  Synergistic and Superimposed Effect of Bone Marrow-Derived Mesenchymal Stem Cells Combined with Fasudil in Experimental Autoimmune Encephalomyelitis.

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Review 10.  The evolving role of neuro-immune interaction in brain repair after cerebral ischemic stroke.

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