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Removing senescent cells as a therapeutic strategy was first verified by killing cells with high p16 Ink4a expression in INK-ATTAC and p16-3MR transgenic mice, which delayed organ dysfunction and prolonged the lifespan in mice aged both prematurely and naturally [5]

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Therefore, above we considered how TLR4 potentially can trigger LPS-induced inflammation caused by the disruption of intestinal integrity through the TIRAP/MyD88 signaling cascade, that leads to the early activation of NF-B (Figure 2, left part)