Summary
Raidoprotective 105 (RP105) was first discovered on the surface of mouse B cells and it has been demonstrated that RP105 can function as an inflammatory regulator in cardiovascular disease (CVD), such as myocardial ischemic reperfusion injury (MI/RI), atherosclerosis and myocardial infarction (MI). As a member of Toll-like receptor (TLR) homolog which is capable of regulating toll-like receptor (TLR4) signaling pathway, RP105 is implicated in various biological processes. Mounting evidence suggests that RP105 regulates the function of TLR4 and phosphoinositide 3-kinase (PI3K) signaling pathways. Here, we review the effect of RP105 on CVD through regulating TLR4/PI3K signaling pathways.
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This study was supported by the National Natural Science Foundation of China (No. 81770360 and No. 81800258)
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The authors declare that there is no conflict of interest with any financial organization or corporation or individual that can inappropriately influence this work.
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Yang, J., Zeng, P., Yang, J. et al. The Role of RP105 in Cardiovascular Disease through Regulating TLR4 and PI3K Signaling Pathways. CURR MED SCI 39, 185–189 (2019). https://doi.org/10.1007/s11596-019-2017-3
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DOI: https://doi.org/10.1007/s11596-019-2017-3