Emerging connectivity of programmed cell death pathways and pulmonary vascular remodelling during pulmonary hypertension

被引:3
作者
Yuan, Meng-Nan [1 ,2 ]
Liu, Ting [1 ,2 ]
Cai, An-Qi [1 ,2 ]
Zhan, Zibo [3 ]
Cheng, Yi-Li [1 ,2 ]
Wang, Qi-Yue [1 ,2 ]
Xia, Yu-Xuan [1 ,2 ]
Shen, Nong-Er [1 ,2 ]
Huang, Ping [1 ,2 ]
Zou, Xiao-Zhou [1 ,2 ]
机构
[1] Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Ctr Clin Pharm,Canc Ctr,Dept Pharm, Shangtang Rd 158, Hangzhou 310014, Zhejiang, Peoples R China
[2] Zhejiang Prov Peoples Hosp, Key Lab Endocrine Gland Dis Zhejiang Prov, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Chinese Med Univ, Sch Pharmaceut Sci, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; autophagy; ferroptosis; necroptosis; programmed cell death; pulmonary hypertension; pulmonary vascular remodelling; pyroptosis; ARTERIAL-HYPERTENSION; MOLECULAR-MECHANISMS; IMMUNE CELLS; DNA-DAMAGE; AUTOPHAGY; APOPTOSIS; BAX; ACTIVATION; DISTINCT; P53;
D O I
10.1111/jcmm.70003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pulmonary hypertension (PH) is a chronic progressive vascular disease characterized by abnormal pulmonary vascular resistance and pulmonary artery pressure. The major structural alteration during PH is pulmonary vascular remodelling, which is mainly caused by the imbalance between proliferation and apoptosis of pulmonary vascular cells. Previously, it was thought that apoptosis was the only type of programmed cell death (PCD). Soon afterward, other types of PCD have been identified, including autophagy, pyroptosis, ferroptosis and necroptosis. In this review, we summarize the role of the above five forms of PCD in mediating pulmonary vascular remodelling, and discuss their guiding significance for PH treatment. The current review could provide a better understanding of the correlation between PCD and pulmonary vascular remodelling, contributing to identify new PCD-associated drug targets for PH.
引用
收藏
页数:12
相关论文
共 116 条
[1]   CCR2/CCR5-mediated macrophage-smooth muscle cell crosstalk in pulmonary hypertension [J].
Abid, Shariq ;
Marcos, Elisabeth ;
Parpaleix, Aurelien ;
Amsellem, Valerie ;
Breau, Marielle ;
Houssaini, Amal ;
Vienney, Nora ;
Lefevre, Marine ;
Derumeaux, Genevieve ;
Evans, Steven ;
Hubeau, Cedric ;
Delcroix, Marion ;
Quarck, Rozenn ;
Adnot, Serge ;
Lipskaia, Larissa .
EUROPEAN RESPIRATORY JOURNAL, 2019, 54 (04)
[2]   Three-dimensional structure of the apoptosome: Implications for assembly, procaspase-9 binding, and activation [J].
Acehan, D ;
Jiang, XJ ;
Morgan, DG ;
Heuser, JE ;
Wang, XD ;
Akey, CW .
MOLECULAR CELL, 2002, 9 (02) :423-432
[3]   In Defense of the Nucleus: NUDT1 and Oxidative DNA Damage in Pulmonary Arterial Hypertension [J].
Agarwal, Stuti ;
Perez, Vinicio A. de Jesus .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2021, 203 (05) :541-542
[4]   GsdmD p30 elicited by caspase-11 during pyroptosis forms pores in membranes [J].
Aglietti, Robin A. ;
Estevez, Alberto ;
Gupta, Aaron ;
Ramirez, Monica Gonzalez ;
Liu, Peter S. ;
Kayagaki, Nobuhiko ;
Ciferri, Claudio ;
Dixit, Vishva M. ;
Dueber, Erin C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (28) :7858-7863
[5]   Neutrophil Extracellular Traps Promote Angiogenesis: Evidence From Vascular Pathology in Pulmonary Hypertension [J].
Aldabbous, Lulwah ;
Abdul-Salam, Vahitha ;
McKinnon, Tom ;
Duluc, Lucie ;
Pepke-Zaba, Joanna ;
Southwood, Mark ;
Ainscough, Alexander J. ;
Hadinnapola, Charaka ;
Wilkins, Martin R. ;
Toshner, Mark ;
Wojciak-Stothard, Beata .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2016, 36 (10) :2078-2087
[6]   Activation of Anoctamin-1 Limits Pulmonary Endothelial Cell Proliferation via p38-Mitogen-activated Protein Kinase-Dependent Apoptosis [J].
Allawzi, Ayed M. ;
Vang, Alexander ;
Clements, Richard T. ;
Jhun, Bong Sook ;
Kue, Nouaying R. ;
Mancini, Thomas J. ;
Landi, Amy K. ;
Terentyev, Dmitry ;
O-Uchi, Jin ;
Comhair, Suzy A. ;
Erzurum, Serpil C. ;
Choudhary, Gaurav .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2018, 58 (05) :658-667
[7]   Triple-tyrosine kinase inhibition attenuates pulmonary arterial hypertension and neointimal formation [J].
Ambade, Anjira S. ;
Jung, Birgit ;
Lee, Dongwon ;
Doods, Henri ;
Wu, Dongmei .
TRANSLATIONAL RESEARCH, 2019, 203 :15-30
[8]   Pyruvate Kinase and Warburg Metabolism in Pulmonary Arterial Hypertension Uncoupled Glycolysis and the Cancer-Like Phenotype of Pulmonary Arterial Hypertension [J].
Archer, Stephen L. .
CIRCULATION, 2017, 136 (25) :2486-2490
[9]   Nets, pulmonary arterial hypertension, and thrombo-inflammation [J].
Baptista de Barros Ribeiro Dourado, Luis Pedro ;
Santos, Mario ;
Moreira-Goncalves, Daniel .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2022, 100 (05) :713-722
[10]   Emerging connectivity of programmed cell death pathways and its physiological implications [J].
Bedoui, Sammy ;
Herold, Marco J. ;
Strasser, Andreas .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2020, 21 (11) :678-695