Related Experiment Video
Updated: Nov 11, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
LncRNA AC105942.1 Downregulates hnRNPA2/B1 to Attenuate Vascular Smooth Muscle Cells Proliferation
Ru-Yi Zhang1, Chang-Meng Wu1, Xiu-Mei Hu1
1Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Abstract:
The abnormal proliferation of vascular smooth muscle cells (VSMCs) is crucial in the atherosclerosis. Although long noncoding RNAs (lncRNAs) are implicated in a variety of diseases, their roles in activation of VSMCs proliferation and vascular disorder diseases are not well understood. In addition, heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNPA2/B1) was reported to participate in lncRNAs-mediated function. Herein, we propose to investigate the role of lncRNA AC105942.1 and hnRNPA2/B1 in pathological VSMCs proliferation and the possible mechanisms in vitro. We have identified that lncRNA AC105942.1 was downregulated and hnRNPA2/B1 was upregulated in atherosclerotic plaques compared with normal artery tissues. Enhanced lncRNA AC105942.1 could noticeably inhibit Ang II-induced VSMCs proliferation. Further investigation suggested that lncRNA AC105942.1 could downregulate the expression of hnRNPA2/B1 and then regulate the level of CDK4 and p27. Taken together, our study indicated that lncRNA AC105942.1 downregulated hnRNPA2B1 to protect against the atherosclerosis by suppressing VSMCs proliferation. LncRNA AC105942.1 and hnRNPA2/B1 could represent potential therapeutic and diagnostic targets to atherosclerosis-related diseases.
Insights
Long noncoding RNA AC105942.1 inhibits vascular smooth muscle cell proliferation, a key factor in atherosclerosis. This study reveals AC105942.1
Area of Science:
- Cardiovascular Biology
- Molecular Biology
- RNA Biology
Background:
- Vascular smooth muscle cell (VSMC) proliferation is central to atherosclerosis.
- The role of long noncoding RNAs (lncRNAs) in VSMC activation and vascular diseases remains unclear.
- Heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNPA2/B1) is involved in lncRNA functions.
Purpose of the Study:
- To investigate the roles of lncRNA AC105942.1 and hnRNPA2/B1 in pathological VSMC proliferation.
- To elucidate the underlying molecular mechanisms in vitro.
- To explore their potential as therapeutic targets for atherosclerosis.
Main Methods:
- Comparative analysis of lncRNA AC105942.1 and hnRNPA2/B1 expression in atherosclerotic plaques versus normal artery tissues.
- In vitro experiments assessing the effect of enhanced lncRNA AC105942.1 on Ang II-induced VSMC proliferation.
- Investigation of the regulatory pathways involving hnRNPA2/B1, CDK4, and p27.
Main Results:
- lncRNA AC105942.1 was downregulated, while hnRNPA2/B1 was upregulated in atherosclerotic plaques.
- Increased lncRNA AC105942.1 expression significantly inhibited Ang II-induced VSMC proliferation.
- lncRNA AC105942.1 was found to downregulate hnRNPA2/B1, subsequently affecting CDK4 and p27 levels.
Conclusions:
- lncRNA AC105942.1 protects against atherosclerosis by suppressing VSMC proliferation via downregulation of hnRNPA2/B1.
- lncRNA AC105942.1 and hnRNPA2/B1 present potential diagnostic and therapeutic targets for atherosclerosis-related diseases.
More Related Videos
08:28Isolation of Primary Patient-specific Aortic Smooth Muscle Cells and Semiquantitative Real-time Contraction Measurements In Vitro
Published on: February 15, 2022
07:49Molecular Analysis of Endothelial-mesenchymal Transition Induced by Transforming Growth Factor-β Signaling
Published on: August 3, 2018
Related Concept Videos
lncRNA - Long Non-coding RNAs
lncRNA - Long Non-coding RNAs
Regulation of Angiogenesis and Blood Supply
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...
MicroRNAs
MicroRNAs