In light of our mission to find novel therapeutic targets to stimulate atherosclerotic
lesion regression, we have reviewed with great interest the data presented by Zhang
et al. in Atherosclerosis which suggest that global inhibition of PLTP activity facilitates the disappearance
of macrophages from regressing atherosclerotic lesions [
[1]
].Keywords
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References
- Inducible phospholipid transfer protein deficiency ameliorates atherosclerosis.Atherosclerosis. 2021; 324: 9-17
- Macrophage phospholipid transfer protein contributes significantly to total plasma phospholipid transfer activity and its deficiency leads to diminished atherosclerotic lesion development.Arterioscler. Thromb. Vasc. Biol. 2007; 27: 578-586
- Inflammatory Ly6Chi monocytes and their conversion to M2 macrophages drive atherosclerosis regression.J. Clin. Invest. 2017; 127: 2904-2915
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Article Info
Publication History
Published online: June 18, 2022
Accepted:
June 10,
2022
Received:
May 23,
2022
Publication stage
In Press Journal Pre-ProofIdentification
Copyright
© 2022 Elsevier B.V. All rights reserved.
ScienceDirect
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- PLTP deficiency-mediated atherosclerosis regression could be related to sphinogosine-1-phosphate reductionAtherosclerosis
- PreviewWe appreciate the positive comment, from Drs. Menno Hoekstra, Ezra J. van der Wel, and Miranda Van Eck, on our recent work of PLTP deficiency-mediated atherosclerosis regression [1]. We agree that the lesion regression effect observed by us can also be attributed to the effect of PLTP deficiency specifically in macrophages, although the mechanism remains unclear.
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