Selected article for: "inflammatory response and LPS stimulation"

Author: Takenouchi, Takato; Kitani, Hiroshi; Suzuki, Shunichi; Nakai, Michiko; Fuchimoto, Dai-ichiro; Tsukimoto, Mitsutoshi; Shinkai, Hiroki; Sato, Mitsuru; Uenishi, Hirohide
Title: Immortalization and Characterization of Porcine Macrophages That Had Been Transduced with Lentiviral Vectors Encoding the SV40 Large T Antigen and Porcine Telomerase Reverse Transcriptase
  • Document date: 2017_8_21
  • ID: 0cqtxqjv_36
    Snippet: Furthermore, we assessed the capacity of the IPKM to produce inflammatory and anti-inflammatory cytokines in response to stimulation with LPS. As was found for the primary PKM, the IPKM secreted substantial amounts of inflammatory cytokines, such as tumor necrosis factor α and IL-1β, after being stimulated with LPS for 24 h (Figure 4 , upper and middle panels). In contrast, although the primary PKM secreted a substantial amount of the anti-infl.....
    Document: Furthermore, we assessed the capacity of the IPKM to produce inflammatory and anti-inflammatory cytokines in response to stimulation with LPS. As was found for the primary PKM, the IPKM secreted substantial amounts of inflammatory cytokines, such as tumor necrosis factor α and IL-1β, after being stimulated with LPS for 24 h (Figure 4 , upper and middle panels). In contrast, although the primary PKM secreted a substantial amount of the anti-inflammatory cytokine IL-10 upon LPS stimulation, the IPKM failed to secrete measurable amounts of IL-10 (Figure 4, lower panel) . These findings suggest that the IPKM primarily displayed the pro-inflammatory M1 phenotype in response to bacterial endotoxins (20) . Further studies using various stimuli are required to determine whether IPKM can exhibit the antiinflammatory M2 phenotype.

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