| Literature DB >> 26874068 |
Xin Chen1, Meihua Yang1, Feiji Sun1, Chao Liang1, Yujia Wei1, Lukang Wang1, Jiong Yue1, Bing Chen1, Song Li1, Shiyong Liu2, Hui Yang3.
Abstract
Cortical tubers in patients with tuberous sclerosis complex (TSC) are highly associated with intractable epilepsy. Recent evidence has shown that transient receptor potential vanilloid 4 (TRPV4) has direct effects on both neurons and glial cells. To understand the role of TRPV4 in pathogenesis of cortical tubers, we investigated the expression patterns of TRPV4 in cortical tubers of TSC compared with normal control cortex (CTX). We found that TRPV4 was clearly up-regulated in cortical tubers at the protein levels. Immunostaining indicated that TRPV4 was specially distributed in abnormal cells, including dysplastic neurons (DNs) and giant cells (GCs). In addition, double immunofluorescent staining revealed that TRPV4 was localized on neurofilament proteins (NF200) positive neurons and glial fibrillary acidic portein (GFAP) positive reactive astrocytes. Moreover, TRPV4 co-localized with both glutamatergic and GABAergic neurons. Furthermore, protein levels of protein kinase C (PKC), but not protein kinase A (PKA), the important upstream factors of the TRPV4, were significantly increased in cortical tubers. Taken together, the overexpression and distribution patterns of TRPV4 may be linked with the intractable epilepsy caused by TSC.Entities:
Keywords: Epilepsy; Protein kinase A; Protein kinase C; Transient receptor potential vanilloid 4; Tuberous sclerosis complex
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Year: 2016 PMID: 26874068 DOI: 10.1016/j.brainres.2016.02.012
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252