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细胞程序性死亡通路与肺动脉高压中肺血管重构的新兴关联。

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

机构信息

Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, China.

Key Laboratory of Endocrine Gland Diseases of Zhejiang Province, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China.

出版信息

J Cell Mol Med. 2024 Aug;28(16):e70003. doi: 10.1111/jcmm.70003.

DOI:10.1111/jcmm.70003
PMID:39153207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11330287/
Abstract

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.

摘要

肺动脉高压(PH)是一种以肺血管阻力和肺动脉压异常为特征的慢性进行性血管疾病。PH 过程中的主要结构改变是肺血管重构,这主要是由肺血管细胞的增殖和凋亡失衡引起的。以前,人们认为细胞凋亡是唯一类型的程序性细胞死亡(PCD)。不久之后,其他类型的 PCD 也被鉴定出来,包括自噬、细胞焦亡、铁死亡和坏死性凋亡。在这篇综述中,我们总结了上述五种 PCD 形式在介导肺血管重构中的作用,并讨论了它们对 PH 治疗的指导意义。目前的综述可以更好地理解 PCD 与肺血管重构之间的相关性,有助于确定 PH 相关的新的 PCD 药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/d22d4d31901b/JCMM-28-e70003-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/53def0f5fe3d/JCMM-28-e70003-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/36c65bd4e91a/JCMM-28-e70003-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/d22d4d31901b/JCMM-28-e70003-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/53def0f5fe3d/JCMM-28-e70003-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/36c65bd4e91a/JCMM-28-e70003-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff5/11330287/d22d4d31901b/JCMM-28-e70003-g002.jpg

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本文引用的文献

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Hypoxia-induced long non-coding RNA plasmacytoma variant translocation 1 upregulation aggravates pulmonary arterial smooth muscle cell proliferation by regulating autophagy via miR-186/Srf/Ctgf and miR-26b/Ctgf signaling pathways.缺氧诱导的长链非编码 RNA 浆细胞瘤变异易位 1 上调通过 miR-186/Srf/Ctgf 和 miR-26b/Ctgf 信号通路调节自噬加重肺动脉平滑肌细胞增殖。
Int J Cardiol. 2023 Jan 1;370:368-377. doi: 10.1016/j.ijcard.2022.09.060. Epub 2022 Sep 27.
2
LncRNA GAS5 promotes spermidine‑induced autophagy through the miRNA‑31‑5p/NAT8L axis in pulmonary artery endothelial cells of patients with CTEPH.长链非编码 RNA GAS5 通过 miRNA-31-5p/NAT8L 轴促进精脒诱导的肺动脉内皮细胞自噬在 CTEPH 患者中。
Mol Med Rep. 2022 Oct;26(4). doi: 10.3892/mmr.2022.12813. Epub 2022 Aug 3.
3
Prostaglandin E1 reduces apoptosis and improves the homing of mesenchymal stem cells in pulmonary arterial hypertension by regulating hypoxia-inducible factor 1 alpha.前列腺素 E1 通过调节低氧诱导因子 1α 减少肺动脉高压中骨髓间充质干细胞的凋亡并改善其归巢。
Stem Cell Res Ther. 2022 Jul 16;13(1):316. doi: 10.1186/s13287-022-03011-x.
4
The mechanism of the imbalance between proliferation and ferroptosis in pulmonary artery smooth muscle cells based on the activation of SLC7A11.基于 SLC7A11 激活的肺动脉平滑肌细胞增殖与铁死亡失衡的机制。
Eur J Pharmacol. 2022 Aug 5;928:175093. doi: 10.1016/j.ejphar.2022.175093. Epub 2022 Jun 11.
5
α-toxin activates the NLRP3 inflammasome by engaging GPI-anchored proteins.α-毒素通过结合 GPI 锚定蛋白激活 NLRP3 炎症小体。
Sci Immunol. 2022 May 20;7(71):eabm1803. doi: 10.1126/sciimmunol.abm1803.
6
Paradoxical roles of caspase-3 in regulating cell survival, proliferation, and tumorigenesis.半胱天冬酶-3 在调节细胞存活、增殖和肿瘤发生中的矛盾作用。
J Cell Biol. 2022 Jun 6;221(6). doi: 10.1083/jcb.202201159. Epub 2022 May 12.
7
Nets, pulmonary arterial hypertension, and thrombo-inflammation.网状内皮系统、肺动脉高压和血栓炎症。
J Mol Med (Berl). 2022 May;100(5):713-722. doi: 10.1007/s00109-022-02197-0. Epub 2022 Apr 20.
8
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J Cell Mol Med. 2022 May;26(9):2633-2645. doi: 10.1111/jcmm.17272. Epub 2022 Apr 7.
9
Circular RNA Sirtuin1 represses pulmonary artery smooth muscle cell proliferation, migration and autophagy to ameliorate pulmonary hypertension via targeting microRNA-145-5p/protein kinase-B3 axis.环状RNA沉默调节蛋白1通过靶向微小RNA-145-5p/蛋白激酶B3轴抑制肺动脉平滑肌细胞增殖、迁移和自噬,从而改善肺动脉高压。
Bioengineered. 2022 Apr;13(4):8759-8771. doi: 10.1080/21655979.2022.2036302.
10
Immune Cells in Pulmonary Arterial Hypertension.免疫细胞在肺动脉高压中的作用。
Heart Lung Circ. 2022 Jul;31(7):934-943. doi: 10.1016/j.hlc.2022.02.007. Epub 2022 Mar 28.