1.The Chemokine CCL2 Promotes Excitatory Synaptic Transmission in Hippocampal Neurons via GluA1 Subunit Trafficking.
En JI ; Yuanyuan ZHANG ; Zhiqiang LI ; Lai WEI ; Zhaofa WU ; Yulong LI ; Xiang YU ; Tian-Jia SONG
Neuroscience Bulletin 2024;40(11):1649-1666
The CC chemokine ligand 2 (CCL2, also known as MCP-1) and its cognate receptor CCR2 have well-characterized roles in chemotaxis. CCL2 has been previously shown to promote excitatory synaptic transmission and neuronal excitability. However, the detailed molecular mechanism underlying this process remains largely unclear. In cultured hippocampal neurons, CCL2 application rapidly upregulated surface expression of GluA1, in a CCR2-dependent manner, assayed using SEP-GluA1 live imaging, surface GluA1 antibody staining, and electrophysiology. Using pharmacology and reporter assays, we further showed that CCL2 upregulated surface GluA1 expression primarily via Gαq- and CaMKII-dependent signaling. Consistently, using i.p. injection of lipopolysaccharide to induce neuroinflammation, we found upregulated phosphorylation of S831 and S845 sites on AMPA receptor subunit GluA1 in the hippocampus, an effect blocked in Ccr2-/- mice. Together, these results provide a mechanism through which CCL2, and other secreted molecules that signal through G-protein coupled receptors, can directly regulate synaptic transmission.
Animals
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Receptors, AMPA/metabolism*
;
Chemokine CCL2/metabolism*
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Hippocampus/drug effects*
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Neurons/drug effects*
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Synaptic Transmission/drug effects*
;
Mice
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Receptors, CCR2/metabolism*
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Protein Transport/drug effects*
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Mice, Inbred C57BL
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Cells, Cultured
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Mice, Knockout
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Excitatory Postsynaptic Potentials/drug effects*
;
Rats
2.Effect of extracts from Radix Trichosanthis on the expression of HBsAg and HBeAg in HepG2.2.15 cells.
Jia CHEN ; Zhaofa XU ; Hongtao OUYANG ; Minyuan PENG ; Ting WU ; Jing LIU ; Yanping LIU ; Huiwen YAN
Journal of Central South University(Medical Sciences) 2012;37(1):38-41
OBJECTIVE:
To investigate the effect of extracts with water and alcohol from Radix Trichosanthis on the cell survival and the expression of hepatitis B surface antigen (HBsAg) and hepatitis B e-antigen (HBeAg) in HepG2.2.15 cell supernatant.
METHODS:
The cell survival rate of HepG2.2.15 cells was detected by MTT assay. The HBsAg and HBeAg in HepG 2.2.15 cell supernatant were evaluated by enzyme linked immunosorbent assay.
RESULTS:
The water and alcohol soluble extracts from Radix Trichosanthis significantly inhibited the levels of HBsAg and HBeAg in HepG2.2.15 cells in a time-and-concentration-dependent manner. However, the therapeutic index of extracts with water from Radix Trichosanthis was better than that in the alcohol group.
CONCLUSION
The activity of water-soluble extract from Radix Trichosanthis is stronger on anti-hepatitis B virus than that of the alcohol-soluble extract.
Antiviral Agents
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pharmacology
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Drugs, Chinese Herbal
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classification
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pharmacology
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Hep G2 Cells
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Hepatitis B Surface Antigens
;
biosynthesis
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Hepatitis B e Antigens
;
biosynthesis
;
Hepatitis B virus
;
drug effects
;
Humans

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