Inflammatory signals induce the expression of tonicity-responsive enhancer binding protein (TonEBP) in microglia.

Citation data:

Journal of neuroimmunology, ISSN: 1872-8421, Vol: 295-296, Page: 21-9

Publication Year:
2016
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Repository URL:
http://scholarworks.unist.ac.kr/handle/201301/19116
PMID:
27235345
DOI:
10.1016/j.jneuroim.2016.04.009
Author(s):
Jeong, Ga Ram; Im, Sun-Kyoung; Bae, Yun-Hee; Park, Eun Su; Jin, Byung Kwan; Kwon, Hyug Moo; Lee, Beom-Joon; Bu, Youngmin; Hur, Eun-Mi; Lee, Byoung Dae
Publisher(s):
Elsevier BV; ELSEVIER SCIENCE BV
Tags:
Medicine; Immunology and Microbiology; Neuroscience; LPS; Microglia; Neuroinflammation; TonEBP
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article description
Tonicity-responsive enhancer (TonE) binding protein (TonEBP) is known as an osmosensitive transcription factor that regulates cellular homeostasis during states of hypo- and hypertonic stress. In addition to its role in osmoadaptation, growing lines of evidence suggest that TonEBP might have tonicity-independent functions. In particular, a number of studies suggest that inflammatory stimuli induce the expression and activation of TonEBP in peripheral immune cells. However, whether TonEBP is expressed in microglia, resident immune cells of the central nervous system, is unknown. Here we show that inflammatory signals induce the expression of TonEBP in microglia both in vitro and in vitro. In cultured primary microglia, treatment with lipopolysaccharide (LPS), interferon-γ, and interleukin 4 increased the expression of TonEBP. Moreover, we found that stereotaxic injection of LPS into the substantia nigra region of rat brain increased TonEBP expression in OX-42-positive cells. Furthermore, expression of TonEBP was induced in OX-42-positive cells in a rat model of transient middle cerebral artery occlusion. Together these results show that the expression of TonEBP is regulated by inflammatory signals in mammalian brain, suggesting that TonEBP might play a part during neuroinflammation.