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©The Author(s) 2024.
World J Psychiatry. Aug 19, 2024; 14(8): 1254-1266
Published online Aug 19, 2024. doi: 10.5498/wjp.v14.i8.1254
Published online Aug 19, 2024. doi: 10.5498/wjp.v14.i8.1254
Figure 2 SPP1 targeted by botulinum toxin type A promotes proliferation and represses apoptosis of lipopolysaccharide-induced microglia.
A-E: Lipopolysaccharide-treated microglia were treated with control short hairpin RNA (shRNA) or SPP1 shRNA, or co-treated with botulinum toxin type A. The expression of SPP1 was analyzed by quantitative real-time polymerase chain reaction (A). The expression of SPP1 was measured by western blot (B). Cell viability was detected by cell counting kit-8 assay (C). Cell apoptosis was examined by flow cytometry (D and E). aP < 0.05, bP < 0.01, cP < 0.001. BTX-A: Botulinum toxin type A.
- Citation: Chen LP, Gui XD, Tian WD, Kan HM, Huang JZ, Ji FH. Botulinum toxin type A-targeted SPP1 contributes to neuropathic pain by the activation of microglia pyroptosis. World J Psychiatry 2024; 14(8): 1254-1266
- URL: https://www.wjgnet.com/2220-3206/full/v14/i8/1254.htm
- DOI: https://dx.doi.org/10.5498/wjp.v14.i8.1254