4.6 Article

m6A Modification-mediated GRAP Regulates Vascular Remodeling in Hypoxic Pulmonary Hypertension

出版社

AMER THORACIC SOC
DOI: 10.1165/rcmb.2021-0429OC

关键词

GRAP; m6A modification; pulmonary arterial hypertension; pulmonary vascular remodeling

资金

  1. Henan Province Medical Science and Technology Research Plan Joint project [LHGJ20200283]
  2. China Postdoctoral Science Foundation [2020M682364]

向作者/读者索取更多资源

This study reveals that m(6)A-modified GRAP mRNA is upregulated in PAH, while GRAP mRNA and protein are downregulated. Overexpression of GRAP alleviates the proliferative and invasive ability of PAH HPASMCs through inhibition of the Ras/ERK signaling pathway. Additionally, METTL14 and the m(6)A binding protein YTHDF2 are significantly increased in PAH.
Pulmonary arterial hypertension (PAH) is characterized by pulmonary vascular remodeling induced by human pulmonary arterial smooth muscle cell (HPASMC) proliferation, migration, and apoptosis resistance. m(6)A (N-6-methyladenosine) is the most prevalent RNA posttranscriptional modification in eukaryotic cells. However, its role in PAH remains elusive. We designed this study to investigate whether m(6)A modification and its effector proteins play a role in pulmonary vascular resistance. Lung samples were used to profile m(6)A concentrations in control subjects and patients with PAH. Bioinformatics analysis, realtime PCR, immunohistochemistry, and Western blotting were used to determine the role of m(6)A effectors in PAH. The biological effects of GRAP modified by m(6)A were investigated using in vitro and in vivo models. Furthermore, RIP-PCR was used to assess the writers and readers of GRAP. In this study, we revealed that m(6)A-modified GRAP mRNA was upregulated in PAH lung samples, cHx/Su-induced mouse models, and hypoxiastimulated HPASMCs; however, GRAP mRNA and protein were abnormally downregulated. Functionally, overexpression of GRAP drastically alleviated the proliferative and invasive ability of PAH HPASMCs through inhibition of the Ras/ERK signaling pathway in vitro and in vivo. In addition, METTL14 (methyltransferase-like 14) and the m(6)A binding protein YTHDF2 were significantly increased in PAH. Moreover, we found that m6A-modified GRAP mRNA was recognized by YTHDF2 to mediate the degradation. GRAP expression was consistently negatively correlated with METTL14 and YTHDF2 in vivo and in vitro. Taken together, for the first time, our findings highlight the function and therapeutic target value of GRAP and extend our understanding of the importance of RNA epigenetics in PAH.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据