后代
生物
巨噬细胞
肿瘤坏死因子α
内科学
内分泌学
医学
免疫学
破骨细胞
怀孕
生物化学
体外
遗传学
受体
作者
Makoto Saburi,Hiroyuki Yamada,Naotoshi Wada,Shinichiro Motoyama,T Sugimoto,Hiroshi Kubota,Daisuke Miyawaki,Noriyuki Wakana,Daisuke Kami,Takehiro Ogata,Satoaki Matoba
出处
期刊:Cells
[MDPI AG]
日期:2021-08-27
卷期号:10 (9): 2224-2224
被引量:3
标识
DOI:10.3390/cells10092224
摘要
Maternal high-fat diet (HFD) modulates vascular remodeling in adult offspring. Here, we investigated the impact of maternal HFD on abdominal aortic aneurysm (AAA) development. Female wild-type mice were fed an HFD or normal diet (ND). AAA was induced in eight-week-old pups using calcium chloride. Male offspring of HFD-fed dams (O-HFD) showed a significant enlargement in AAA compared with the offspring of ND-fed dams (O-ND). Positive-staining cells for tartrate-resistant acid phosphate (TRAP) and matrix metalloproteinase (MMP) activity were significantly increased in O-HFD. The pharmacological inhibition of osteoclastogenesis abolished the exaggerated AAA development in O-HFD. The in vitro tumor necrosis factor-α-induced osteoclast-like differentiation of bone marrow-derived macrophages showed a higher number of TRAP-positive cells and osteoclast-specific gene expressions in O-HFD. Consistent with an increased expression of nuclear factor of activated T cells 1 (NFATc1) in O-HFD, the nuclear protein expression of interferon regulatory factor 8 (IRF8), a transcriptional repressor, were much lower, with significantly increased H3K27me3 marks at the promoter region. The enhancer of zeste homolog 2 inhibitor treatment restored IRF8 expression, resulting in no difference in NFATc1 and TRAP expressions between the two groups. Our findings demonstrate that maternal HFD augments AAA expansion, accompanied by exaggerated osteoclast-like macrophage accumulation, suggesting the possibility of macrophage skewing via epigenetic reprogramming.
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