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KLF2 Promotes Neutrophil Apoptosis in Mice with Myocardial ischemia-reperfusion Injury by Upregulating Notch1.

作者信息

Nie Furu, Deng Xu

机构信息

Cardiovascular Department III, Hunan Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Changsha, 410006, Hunan, China.

Department of Cardiology, the Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, China.

出版信息

Cell Biochem Biophys. 2025 Sep 12. doi: 10.1007/s12013-025-01889-x.

DOI:10.1007/s12013-025-01889-x
PMID:40938482
Abstract
摘要

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KLF2 Promotes Neutrophil Apoptosis in Mice with Myocardial ischemia-reperfusion Injury by Upregulating Notch1.KLF2通过上调Notch1促进心肌缺血再灌注损伤小鼠中性粒细胞凋亡。
Cell Biochem Biophys. 2025 Sep 12. doi: 10.1007/s12013-025-01889-x.
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J Am Heart Assoc. 2025 Jul;14(13):e038142. doi: 10.1161/JAHA.124.038142. Epub 2025 Jun 27.
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本文引用的文献

1
KLF2 controls the apoptosis of neutrophils and is associated with disease activity of systemic lupus erythematosus.KLF2控制中性粒细胞的凋亡,并与系统性红斑狼疮的疾病活动相关。
Arthritis Res Ther. 2024 Dec 19;26(1):222. doi: 10.1186/s13075-024-03461-z.
2
Myocardial ischemia-reperfusion injury: The balance mechanism between mitophagy and NLRP3 inflammasome.心肌缺血再灌注损伤:自噬与 NLRP3 炎性小体之间的平衡机制。
Life Sci. 2024 Oct 15;355:122998. doi: 10.1016/j.lfs.2024.122998. Epub 2024 Aug 20.
3
"Find Me" and "Eat Me" signals: tools to drive phagocytic processes for modulating antitumor immunity.
“找我”和“吃我”信号:用于调节抗肿瘤免疫的吞噬过程的工具。
Cancer Commun (Lond). 2024 Jul;44(7):791-832. doi: 10.1002/cac2.12579. Epub 2024 Jun 23.
4
WTAP-mediated mA modification of lncRNA Snhg1 improves myocardial ischemia-reperfusion injury via miR-361-5p/OPA1-dependent mitochondrial fusion.WTAP 通过介导 lncRNA Snhg1 的 mA 修饰作用改善心肌缺血再灌注损伤,其作用机制是通过 miR-361-5p/OPA1 依赖性线粒体融合。
J Transl Med. 2024 May 25;22(1):499. doi: 10.1186/s12967-024-05330-4.
5
MSC-Derived Exosomes Mitigate Myocardial Ischemia/Reperfusion Injury by Reducing Neutrophil Infiltration and the Formation of Neutrophil Extracellular Traps.MSC 来源的外泌体通过减少中性粒细胞浸润和中性粒细胞细胞外陷阱的形成来减轻心肌缺血/再灌注损伤。
Int J Nanomedicine. 2024 Mar 5;19:2071-2090. doi: 10.2147/IJN.S436925. eCollection 2024.
6
B cell subsets contribute to myocardial protection by inducing neutrophil apoptosis after ischemia and reperfusion.B 细胞亚群通过在缺血再灌注后诱导中性粒细胞凋亡来发挥心肌保护作用。
JCI Insight. 2024 Feb 22;9(4):e167201. doi: 10.1172/jci.insight.167201.
7
Dying to Defend: Neutrophil Death Pathways and their Implications in Immunity.《垂死防御:中性粒细胞死亡途径及其在免疫中的意义》。
Adv Sci (Weinh). 2024 Feb;11(8):e2306457. doi: 10.1002/advs.202306457. Epub 2023 Dec 3.
8
Inflammation in Myocardial Ischemia/Reperfusion Injury: Underlying Mechanisms and Therapeutic Potential.心肌缺血/再灌注损伤中的炎症:潜在机制与治疗潜力
Antioxidants (Basel). 2023 Oct 31;12(11):1944. doi: 10.3390/antiox12111944.
9
FGF2 Alleviates Microvascular Ischemia-Reperfusion Injury by KLF2-mediated Ferroptosis Inhibition and Antioxidant Responses.FGF2 通过 KLF2 介导的铁死亡抑制和抗氧化反应减轻微血管缺血再灌注损伤。
Int J Biol Sci. 2023 Aug 21;19(13):4340-4359. doi: 10.7150/ijbs.85692. eCollection 2023.
10
Kindlin-2 controls angiogenesis through modulating Notch1 signaling.Kindlin-2 通过调节 Notch1 信号通路控制血管生成。
Cell Mol Life Sci. 2023 Jul 22;80(8):223. doi: 10.1007/s00018-023-04866-w.