A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification

Summary: Based on high-throughput transcriptomic sequencing, SNHG3 was among the most highly expressed long noncoding RNAs in calcific aortic valve disease. SNHG3 upregulation was verified in human and mouse calcified aortic valves. Moreover, in vivo and in vitro studies showed SNHG3 silencing marke...

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Main Authors: Long Chen, MD, Hanning Liu, MD, PhD, Cheng Sun, MD, PhD, Jianqiu Pei, PhD, Jun Li, MD, Yue Li, PhD, Ke Wei, MD, PhD, Xiaoyi Wang, MD, Peng Wang, MD, Fangzhou Li, MD, Shujie Gai, MD, PhD, Yan Zhao, MD, Zhe Zheng, MD, PhD
Format: Article
Language:English
Published: Elsevier 2022-09-01
Series:JACC: Basic to Translational Science
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2452302X22002297
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author Long Chen, MD
Hanning Liu, MD, PhD
Cheng Sun, MD, PhD
Jianqiu Pei, PhD
Jun Li, MD
Yue Li, PhD
Ke Wei, MD, PhD
Xiaoyi Wang, MD
Peng Wang, MD
Fangzhou Li, MD
Shujie Gai, MD, PhD
Yan Zhao, MD
Zhe Zheng, MD, PhD
author_facet Long Chen, MD
Hanning Liu, MD, PhD
Cheng Sun, MD, PhD
Jianqiu Pei, PhD
Jun Li, MD
Yue Li, PhD
Ke Wei, MD, PhD
Xiaoyi Wang, MD
Peng Wang, MD
Fangzhou Li, MD
Shujie Gai, MD, PhD
Yan Zhao, MD
Zhe Zheng, MD, PhD
author_sort Long Chen, MD
collection DOAJ
description Summary: Based on high-throughput transcriptomic sequencing, SNHG3 was among the most highly expressed long noncoding RNAs in calcific aortic valve disease. SNHG3 upregulation was verified in human and mouse calcified aortic valves. Moreover, in vivo and in vitro studies showed SNHG3 silencing markedly ameliorated aortic valve calcification. In-depth functional assays showed SNHG3 physically interacted with polycomb repressive complex 2 to suppress the H3K27 trimethylation BMP2 locus, which in turn activated BMP2 expression and signaling pathways. Taken together, SNHG3 promoted aortic valve calcification by upregulating BMP2, which might be a novel therapeutic target in human calcific aortic valve disease.
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spelling doaj.art-3129fe2e76f44c7a89427c5cf1419cbe2022-12-22T03:48:09ZengElsevierJACC: Basic to Translational Science2452-302X2022-09-0179899914A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve CalcificationLong Chen, MD0Hanning Liu, MD, PhD1Cheng Sun, MD, PhD2Jianqiu Pei, PhD3Jun Li, MD4Yue Li, PhD5Ke Wei, MD, PhD6Xiaoyi Wang, MD7Peng Wang, MD8Fangzhou Li, MD9Shujie Gai, MD, PhD10Yan Zhao, MD11Zhe Zheng, MD, PhD12Department of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaDepartment of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaAddress for correspondence: Dr Zhe Zheng, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Beilishi Road, Xicheng District, Beijing, PR China.; Department of Cardiovascular Surgery, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Disease, China and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of ChinaSummary: Based on high-throughput transcriptomic sequencing, SNHG3 was among the most highly expressed long noncoding RNAs in calcific aortic valve disease. SNHG3 upregulation was verified in human and mouse calcified aortic valves. Moreover, in vivo and in vitro studies showed SNHG3 silencing markedly ameliorated aortic valve calcification. In-depth functional assays showed SNHG3 physically interacted with polycomb repressive complex 2 to suppress the H3K27 trimethylation BMP2 locus, which in turn activated BMP2 expression and signaling pathways. Taken together, SNHG3 promoted aortic valve calcification by upregulating BMP2, which might be a novel therapeutic target in human calcific aortic valve disease.http://www.sciencedirect.com/science/article/pii/S2452302X22002297BMP2 pathwaycalcific aortic valve diseaselong noncoding RNAosteoblast differentiationtherapeutic target
spellingShingle Long Chen, MD
Hanning Liu, MD, PhD
Cheng Sun, MD, PhD
Jianqiu Pei, PhD
Jun Li, MD
Yue Li, PhD
Ke Wei, MD, PhD
Xiaoyi Wang, MD
Peng Wang, MD
Fangzhou Li, MD
Shujie Gai, MD, PhD
Yan Zhao, MD
Zhe Zheng, MD, PhD
A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification
JACC: Basic to Translational Science
BMP2 pathway
calcific aortic valve disease
long noncoding RNA
osteoblast differentiation
therapeutic target
title A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification
title_full A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification
title_fullStr A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification
title_full_unstemmed A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification
title_short A Novel LncRNA SNHG3 Promotes Osteoblast Differentiation Through BMP2 Upregulation in Aortic Valve Calcification
title_sort novel lncrna snhg3 promotes osteoblast differentiation through bmp2 upregulation in aortic valve calcification
topic BMP2 pathway
calcific aortic valve disease
long noncoding RNA
osteoblast differentiation
therapeutic target
url http://www.sciencedirect.com/science/article/pii/S2452302X22002297
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