FASEB J. 2025 Nov 15;39(21):e71182. doi: 10.1096/fj.202501781RR.
ABSTRACT
Wilms’ tumor 1-associating protein (WTAP), a core component of the N6-methyladenosine (m6A) methyltransferase complex, plays a crucial role in various biological processes. However, functional studies of WTAP in atherosclerosis development are largely unknown. Here, we demonstrate that WTAP expression was elevated in lipopolysaccharide (LPS)-stimulated macrophages and atherosclerotic lesions of apolipoprotein E-deficient (ApoE-/-) mice. To explore its functional role, we employed AAV8-mediated in vivo knockdown and siRNA-mediated in vitro silencing, which revealed that WTAP deficiency attenuated macrophage apoptosis and reduced atherosclerotic plaque formation. Mechanistically, we identified myosin heavy chain 11 (MYH11) as a mediator of WTAP-induced macrophage apoptosis. Notably, WTAP upregulated MYH11 expression in macrophages through an m6A-independent mechanism. These results delineate a new molecular paradigm that macrophage WTAP promotes macrophage apoptosis and atherosclerosis by increasing MYH11 expression, indicating that WTAP may be a potential therapeutic target against atherosclerosis.
PMID:41148185 | DOI:10.1096/fj.202501781RR
