The Contribution of TRPV4 Channels to Astrocyte Volume Regulation and Brain Edema Formation
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30367945
DOI
10.1016/j.neuroscience.2018.10.028
PII: S0306-4522(18)30691-2
Knihovny.cz E-zdroje
- Klíčová slova
- TRPV4 channels, astrocytes, ischemia, volume regulation,
- MeSH
- astrocyty metabolismus patologie MeSH
- edém mozku etiologie metabolismus patologie MeSH
- infarkt arteria cerebri media metabolismus patologie MeSH
- ischemie mozku komplikace MeSH
- kationtové kanály TRPV genetika metabolismus MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- primární buněčná kultura MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- kationtové kanály TRPV MeSH
- Trpv4 protein, mouse MeSH Prohlížeč
Transient receptor potential vanilloid type 4 (TRPV4) channels are involved in astrocyte volume regulation; however, only limited data exist about its mechanism in astrocytes in situ. We performed middle cerebral artery occlusion in adult mice, where we found twice larger edema 1 day after the insult in trpv4-/- mice compared to the controls, which was quantified using magnetic resonance imaging. This result suggests disrupted volume regulation in the brain cells in trpv4-/- mice leading to increased edema formation. The aim of our study was to elucidate whether TRPV4 channel-based volume regulation occurs in astrocytes in situ and whether the disrupted volume regulation in trpv4-/- mice might lead to higher edema formation after brain ischemia. For our experiments, we used trpv4-/- mice crossed with transgenic mice expressing enhanced green fluorescent protein (EGFP) under the control of the glial fibrillary acidic protein promoter, which leads to astrocyte visualization by EGFP expression. For quantification of astrocyte volume changes, we used two-dimensional (2D) and three-dimensional (3D) morphometrical approaches and a quantification algorithm based on fluorescence intensity changes during volume alterations induced by hypotonicity or by oxygen-glucose deprivation. In contrast to in vitro experiments, we found little evidence of the contribution of TRPV4 channels to volume regulation in astrocytes in situ in adult mice. Moreover, we only found a rare expression of TRPV4 channels in adult mouse astrocytes. Our data suggest that TRPV4 channels are not involved in astrocyte volume regulation in situ; however, they play a protective role during the ischemia-induced brain edema formation.
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