• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

钙非依赖性磷脂酶 Aβ(iPLAβ)对免疫细胞的影响。

The Impact of the Ca-Independent Phospholipase Aβ (iPLAβ) on Immune Cells.

机构信息

Department of Cell, Developmental and Integrative Biology, Comprehensive Diabetes Center, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Biomolecules. 2021 Apr 15;11(4):577. doi: 10.3390/biom11040577.

DOI:10.3390/biom11040577
PMID:33920898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8071342/
Abstract

The Ca-independent phospholipase Aβ (iPLAβ) is a member of the PLA family that has been proposed to have roles in multiple biological processes including membrane remodeling, cell proliferation, bone formation, male fertility, cell death, and signaling. Such involvement has led to the identification of iPLAβ activation in several diseases such as cancer, cardiovascular abnormalities, glaucoma, periodontitis, neurological disorders, diabetes, and other metabolic disorders. More recently, there has been heightened interest in the role that iPLAβ plays in promoting inflammation. Recognizing the potential contribution of iPLAβ in the development of autoimmune diseases, we review this issue in the context of an iPLAβ link with macrophages and T-cells.

摘要

钙非依赖性磷脂酶 Aβ(iPLAβ)是 PLA 家族的一员,被认为在多种生物过程中发挥作用,包括膜重塑、细胞增殖、骨形成、男性生育力、细胞死亡和信号转导。这种参与导致在几种疾病中鉴定出 iPLAβ 的激活,如癌症、心血管异常、青光眼、牙周炎、神经紊乱、糖尿病和其他代谢紊乱。最近,人们对 iPLAβ 在促进炎症中的作用产生了浓厚的兴趣。鉴于 iPLAβ 在自身免疫性疾病发展中的潜在贡献,我们在与巨噬细胞和 T 细胞的联系的背景下审查了这个问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/8c6bc3cee31e/biomolecules-11-00577-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/31d3aae07a74/biomolecules-11-00577-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/eed48b2655c0/biomolecules-11-00577-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/8c6bc3cee31e/biomolecules-11-00577-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/31d3aae07a74/biomolecules-11-00577-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/eed48b2655c0/biomolecules-11-00577-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b98/8071342/8c6bc3cee31e/biomolecules-11-00577-g003.jpg

相似文献

1
The Impact of the Ca-Independent Phospholipase Aβ (iPLAβ) on Immune Cells.钙非依赖性磷脂酶 Aβ(iPLAβ)对免疫细胞的影响。
Biomolecules. 2021 Apr 15;11(4):577. doi: 10.3390/biom11040577.
2
Inhibition of Ca2+-independent phospholipase A2β (iPLA2β) ameliorates islet infiltration and incidence of diabetes in NOD mice.抑制非钙依赖性磷脂酶A2β(iPLA2β)可改善非肥胖糖尿病(NOD)小鼠的胰岛浸润和糖尿病发病率。
Diabetes. 2015 Feb;64(2):541-54. doi: 10.2337/db14-0097. Epub 2014 Sep 11.
3
Analyses of Calcium-Independent Phospholipase Abeta (iPLAβ) in Biological Systems.生物系统中钙非依赖性磷脂酶Aβ(iPLAβ)的分析
Methods Enzymol. 2017;583:119-141. doi: 10.1016/bs.mie.2016.09.001. Epub 2016 Oct 18.
4
Macrophage polarization is linked to Ca-independent phospholipase Aβ-derived lipids and cross-cell signaling in mice.巨噬细胞极化与 Ca 非依赖性磷脂酶 Aβ衍生脂质和小鼠中的细胞间信号转导有关。
J Lipid Res. 2020 Feb;61(2):143-158. doi: 10.1194/jlr.RA119000281. Epub 2019 Dec 9.
5
Mice with Genetic Deletion of Group VIA Phospholipase A2β Exhibit Impaired Macrophage Function and Increased Parasite Load in Trypanosoma cruzi-Induced Myocarditis.通过基因敲除VIA组磷脂酶A2β构建的小鼠在克氏锥虫诱发的心肌炎中表现出巨噬细胞功能受损和寄生虫负荷增加。
Infect Immun. 2016 Mar 24;84(4):1137-1142. doi: 10.1128/IAI.01564-15. Print 2016 Apr.
6
Polarization of Macrophages toward M2 Phenotype Is Favored by Reduction in iPLA2β (Group VIA Phospholipase A2).巨噬细胞向M2表型的极化因iPLA2β(ⅥA组磷脂酶A2)减少而受到促进。
J Biol Chem. 2016 Oct 28;291(44):23268-23281. doi: 10.1074/jbc.M116.754945. Epub 2016 Sep 20.
7
Progesterone-induced Acrosome Exocytosis Requires Sequential Involvement of Calcium-independent Phospholipase A2β (iPLA2β) and Group X Secreted Phospholipase A2 (sPLA2).孕酮诱导的顶体胞吐作用需要钙非依赖性磷脂酶A2β(iPLA2β)和X组分泌型磷脂酶A2(sPLA2)的顺序参与。
J Biol Chem. 2016 Feb 5;291(6):3076-89. doi: 10.1074/jbc.M115.677799. Epub 2015 Dec 11.
8
Cytosolic group IVA and calcium-independent group VIA phospholipase A2s act on distinct phospholipid pools in zymosan-stimulated mouse peritoneal macrophages.胞质 IVA 组和钙非依赖性 VIA 组磷酯酶 A2s 在酵母聚糖刺激的鼠腹膜巨噬细胞中作用于不同的磷脂池。
J Immunol. 2014 Jan 15;192(2):752-62. doi: 10.4049/jimmunol.1302267. Epub 2013 Dec 13.
9
Ca-independent phospholipase Aβ-derived PGE contributes to osteogenesis.钙离子非依赖型磷脂酶 Aβ 衍生的 PGE 有助于成骨。
Prostaglandins Other Lipid Mediat. 2022 Feb;158:106605. doi: 10.1016/j.prostaglandins.2021.106605. Epub 2021 Dec 16.
10
Deficiency of Group VIA Phospholipase A2 (iPLA2β) Renders Susceptibility for Chemical-Induced Colitis.第六组A类磷脂酶A2(iPLA2β)缺乏导致对化学诱导性结肠炎的易感性。
Dig Dis Sci. 2015 Dec;60(12):3590-602. doi: 10.1007/s10620-015-3807-5. Epub 2015 Jul 17.

引用本文的文献

1
Lipid Droplets, Phospholipase A, Arachidonic Acid, and Atherosclerosis.脂滴、磷脂酶A、花生四烯酸与动脉粥样硬化
Biomedicines. 2021 Dec 13;9(12):1891. doi: 10.3390/biomedicines9121891.

本文引用的文献

1
Urocortin participates in LPS-induced apoptosis of THP-1 macrophages via S1P-cPLA2 signaling pathway.尿皮质素通过鞘氨醇-1-磷酸-胞浆型磷脂酶A2信号通路参与脂多糖诱导的THP-1巨噬细胞凋亡。
Eur J Pharmacol. 2020 Nov 15;887:173559. doi: 10.1016/j.ejphar.2020.173559. Epub 2020 Sep 16.
2
Lipid mediators and biomarkers associated with type 1 diabetes development.与 1 型糖尿病发展相关的脂质介质和生物标志物。
JCI Insight. 2020 Aug 20;5(16):138034. doi: 10.1172/jci.insight.138034.
3
Phospholipid Arachidonic Acid Remodeling During Phagocytosis in Mouse Peritoneal Macrophages.
小鼠腹腔巨噬细胞吞噬作用过程中的磷脂花生四烯酸重塑
Biomedicines. 2020 Aug 5;8(8):274. doi: 10.3390/biomedicines8080274.
4
Single-cell RNA sequencing of murine islets shows high cellular complexity at all stages of autoimmune diabetes.单细胞 RNA 测序显示,在自身免疫性糖尿病的所有阶段,胰岛具有高度的细胞复杂性。
J Exp Med. 2020 Jun 1;217(6). doi: 10.1084/jem.20192362.
5
Cross-presentation of exogenous antigens on MHC I molecules.外源性抗原在 MHC I 分子上的交叉呈递。
Curr Opin Immunol. 2020 Jun;64:1-8. doi: 10.1016/j.coi.2019.12.005. Epub 2020 Jan 9.
6
Macrophage polarization is linked to Ca-independent phospholipase Aβ-derived lipids and cross-cell signaling in mice.巨噬细胞极化与 Ca 非依赖性磷脂酶 Aβ衍生脂质和小鼠中的细胞间信号转导有关。
J Lipid Res. 2020 Feb;61(2):143-158. doi: 10.1194/jlr.RA119000281. Epub 2019 Dec 9.
7
Therapeutic Potential of ω-3 Polyunsaturated Fatty Acids in Human Autoimmune Diseases.ω-3 多不饱和脂肪酸在人类自身免疫性疾病中的治疗潜力。
Front Immunol. 2019 Sep 27;10:2241. doi: 10.3389/fimmu.2019.02241. eCollection 2019.
8
The origins and non-canonical functions of macrophages in development and regeneration.巨噬细胞在发育和再生中的起源和非经典功能。
Development. 2019 May 2;146(9):dev156000. doi: 10.1242/dev.156000.
9
SLPI Inhibits ATP-Mediated Maturation of IL-1β in Human Monocytic Leukocytes: A Novel Function of an Old Player.SLPI 抑制人单核白血病细胞中 ATP 介导的 IL-1β成熟:旧分子的新功能。
Front Immunol. 2019 Apr 4;10:664. doi: 10.3389/fimmu.2019.00664. eCollection 2019.
10
Substrate-Specific Inhibition Constants for Phospholipase A Acting on Unique Phospholipid Substrates in Mixed Micelles and Membranes Using Lipidomics.基于脂质组学的混合胶束和膜中独特磷脂底物上的磷脂酶 A 的底物特异性抑制常数。
J Med Chem. 2019 Feb 28;62(4):1999-2007. doi: 10.1021/acs.jmedchem.8b01568. Epub 2019 Feb 4.