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Review
. 2019 Jun 1;20(11):2703.
doi: 10.3390/ijms20112703.

Akt Signaling in Macrophage Polarization, Survival, and Atherosclerosis

Affiliations
Review

Akt Signaling in Macrophage Polarization, Survival, and Atherosclerosis

MacRae F Linton et al. Int J Mol Sci. .

Abstract

The PI3K/Akt pathway plays a crucial role in the survival, proliferation, and migration of macrophages, which may impact the development of atherosclerosis. Changes in Akt isoforms or modulation of the Akt activity levels in macrophages significantly affect their polarization phenotype and consequently atherosclerosis in mice. Moreover, the activity levels of Akt signaling determine the viability of monocytes/macrophages and their resistance to pro-apoptotic stimuli in atherosclerotic lesions. Therefore, elimination of pro-apoptotic factors as well as factors that antagonize or suppress Akt signaling in macrophages increases cell viability, protecting them from apoptosis, and this markedly accelerates atherosclerosis in mice. In contrast, inhibition of Akt signaling by the ablation of Rictor in myeloid cells, which disrupts mTORC2 assembly, significantly decreases the viability and proliferation of blood monocytes and macrophages with the suppression of atherosclerosis. In addition, monocytes and macrophages exhibit a threshold effect for Akt protein levels in their ability to survive. Ablation of two Akt isoforms, preserving only a single Akt isoform in myeloid cells, markedly compromises monocyte and macrophage viability, inducing monocytopenia and diminishing early atherosclerosis. These recent advances in our understanding of Akt signaling in macrophages in atherosclerosis may have significant relevance in the burgeoning field of cardio-oncology, where PI3K/Akt inhibitors being tested in cancer patients can have significant cardiovascular and metabolic ramifications.

Keywords: Akt signaling; apoptosis; atherosclerosis; macrophages; polarization; survival.

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Conflict of interest statement

The authors declare that our research was conducted and performed in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
The survival signaling pathways related to the PI3K/Akt pathway in mouse macrophages. The black arrows show the direction of signaling, T-bars indicate the suppression of following signaling and dotted arrows are possible phosphorylation of IκB with release the complex into nucleus whereas the red arrows are the part of signaling we discussed in our review.

References

    1. Libby P. Inflammation in atherosclerosis. Arterioscl. Thromb Vasc. Biol. 2012;32:2045–2051. doi: 10.1161/ATVBAHA.108.179705. - DOI - PMC - PubMed
    1. Hansson Göran K., Jonasson L. The discovery of cellular immunity in the atherosclerotic plaque. Arterioscl. Thromb Vasc. Biol. 2009;29:1714–1717. doi: 10.1161/ATVBAHA.108.179713. - DOI - PubMed
    1. Tabas I., Bornfeldt K.E. Macrophage phenotype and function in different stages of atherosclerosis. Circulation Res. 2016;118:653–667. doi: 10.1161/CIRCRESAHA.115.306256. - DOI - PMC - PubMed
    1. Kockx M.M., Herman A.G. Apoptosis in atherosclerosis: Beneficial or detrimental? Cardiovasc Res. 2000;45:736–746. doi: 10.1016/S0008-6363(99)00235-7. - DOI - PubMed
    1. Fruman D.A., Chiu H., Hopkins B.D., Bagrodia S., Cantley L.C., Abraham R.T. The pi3k pathway in human disease. Cell. 2017;170:605–635. doi: 10.1016/j.cell.2017.07.029. - DOI - PMC - PubMed

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