Subcellular localization patterns of transglutaminase 2 in astrocytes and neurons are differentially altered by hypoxia. Issue 18 (13th December 2017)

• Record Type: Journal Article
• Authors: Yunes-Medina, Laura; Feola, Julianne; Johnson, Gail V.W.
• Is Part Of: NeuroReport. Volume 28:Issue 18(2017)
• Publication Date: 2017-12-13
• Subjects: extracellular -- ischemia -- localization -- nuclear -- oxygen/glucose deprivation -- transglutaminase 2; Neurosciences -- Periodicals; Nervous system -- Periodicals; Neurophysiology -- Periodicals; Nervous System Diseases -- Periodicals; Nervous System Physiological Phenomena -- Periodicals; Neurosciences -- Periodicals; 616.805
• DOI: 10.1097/WNR.0000000000000895
• Languages: English
• ISSNs: 0959-4965

Abstract

Abstract : The multifunctional protein transglutaminase 2 (TG2) has been widely implicated as a modulator of cellular viability. Specifically, TG2 expression is beneficial to neuronal survival following an ischemic injury, whereas the opposite is true in astrocytes. Furthermore, its role in mediating cell death and survival processes has been suggested to be dependent on its subcellular localization. Therefore, the aim of this study was to examine the subcellular localization patterns of neuronal and astrocytic TG2 in ischemia-relevant conditions. We found that nuclear levels of TG2 were significantly increased in neurons, but reduced in astrocytes, in response to hypoxia. In addition, there were no changes in extracellular TG2 in astrocytes exposed to hypoxia. Thus, these findings demonstrate a difference in the subcellular localization pattern of TG2 in neurons and astrocytes in ischemia-relevant conditions and provide further avenues for investigation into the role of TG2 in mediating cellular viability.