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Itaconate inhibits corticosterone-induced necroptosis and neuroinflammation via up-regulating menin in HT22 cells.
- Source :
-
Journal of physiology and biochemistry [J Physiol Biochem] 2024 May; Vol. 80 (2), pp. 393-405. Date of Electronic Publication: 2024 Mar 01. - Publication Year :
- 2024
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Abstract
- Corticosterone (CORT) damages hippocampal neurons as well as induces neuroinflammation. The tricarboxylic acid cycle metabolite itaconate has an anti-inflammatory role. Necroptosis is a form of programmed cell death, also known as inflammatory cell death. Menin is a multifunctional scaffold protein, which deficiency aggravates neuroinflammation. In this study, we explored whether itaconate inhibits CORT-induced neuroinflammation as well as necroptosis and further investigated the mediatory role of Menin in this protective effect of itaconate by using an exposure of CORT to HT22 cells (a hippocampal neuronal cell line). The viability of HT22 cells was examined by the cell counting kit 8 (CCK-8). The morphology of HT22 cells was observed by transmission electron microscope (TEM). The expressions of necroptosis-related proteins (p-RIP1/RIP1, p-RIP3/RIP3, and p-MLKL/MLKL) were evaluated by western blotting. The contents of inflammatory factors were detected by an enzyme-linked immunosorbent assay (ELISA) kit. Our results showed that CORT increases the contents of pro-inflammatory factors (IL-1β, TNF-α) as well as decreases the contents of anti-inflammatory factors (IL-4, IL-10) in HT22 cells. We also found that CORT increases the expressions of necroptosis-related proteins (p-RIP1/RIP1, p-RIP3/RIP3, and p-MLKL/MLKL) and decreases the cell viability in HT22 cells, indicating that CORT induces necroptosis in HT22 cells. Itaconate improves CORT-induced neuroinflammation and necroptosis. Furthermore, itaconate upregulates the expression of Menin in CORT-exposed HT22 cells. Importantly, silencing Menin abolishes the antagonistic effect of itaconate on CORT-induced necroptosis and neuroinflammation. In brief, these results indicated that itaconate protects HT22 cells against CORT-induced neuroinflammation and necroptosis via upregulating Menin.<br /> (© 2024. The Author(s) under exclusive licence to University of Navarra.)
- Subjects :
- Animals
Mice
Anti-Inflammatory Agents pharmacology
Cell Line
Cell Survival drug effects
Hippocampus metabolism
Hippocampus drug effects
Hippocampus pathology
Neuroinflammatory Diseases metabolism
Neuroinflammatory Diseases drug therapy
Neuroinflammatory Diseases chemically induced
Neuroinflammatory Diseases pathology
Neurons drug effects
Neurons metabolism
Neurons pathology
Receptor-Interacting Protein Serine-Threonine Kinases metabolism
Receptor-Interacting Protein Serine-Threonine Kinases genetics
Succinates pharmacology
Corticosterone
Necroptosis drug effects
Proto-Oncogene Proteins metabolism
Proto-Oncogene Proteins genetics
Up-Regulation drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1877-8755
- Volume :
- 80
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of physiology and biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 38427168
- Full Text :
- https://doi.org/10.1007/s13105-024-01012-3