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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 38 Issue 3
Mar.  2022
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Article Contents

Mechanism of action of bone morphogenetic protein 9 in portopulmonary hypertension

DOI: 10.3969/j.issn.1001-5256.2022.03.037
Research funding:

Foundation of Science and Technology Commission of Jilin Province (20190201065JC)

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  • Corresponding author: WEN Xiaoyu, xywen@jlu.edu.cn(ORCID: 0000-0003-2109-1557)
  • Received Date: 2021-07-24
  • Accepted Date: 2021-09-08
  • Published Date: 2022-03-20
  • Portopulmonary hypertension (POPH) is an increase in pulmonary artery pressure that occurs on the basis of portal hypertension. As a member of the BMP family, bone morphogenetic protein 9 (BMP9) not only has the osteogenic activity, but can also protect endothelial integrity and maintain vascular homeostasis. This article reviews the pathogenesis of POPH, the physiological expression and role of BMP9, and related research advances in the BMP9 signaling pathway and its involvement in pulmonary hypertension and vascular remodeling, thereby exploring the possibility of BMP9 as a new biomarker for POPH to assist in the diagnosis of POPH.

     

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