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蛋白酪氨酸磷酸酶非受体型2负向调控巨噬细胞免疫反应和细胞生物能量学。

PTPN2 Negatively Regulates Macrophage Immune Responses and Cellular Bioenergetics.

作者信息

Vinette Valerie, Zolotarov Yevgen, Poirier Alexandre, Cordova Zuzet Martinez, Aubry Isabelle, Tremblay Michel L

机构信息

Department of Biochemistry, McGill University, Montreal, Canada.

Rosalind and Morris Goodman Cancer Institute, McGill University, Montreal, Canada.

出版信息

FASEB J. 2025 May 15;39(9):e70536. doi: 10.1096/fj.202402405R.

Abstract

PTPN2 is encoded by the protein tyrosine phosphatase N2 (also known as TC-PTP) and is a negative regulator of cytokine signaling and macrophage differentiation. In the past decade, our work and others, including several pharmaceuticals, have emphasized that inhibition of PTPN2 and PTPN1 (also known as PTP1B) may act as a new first-of-class cancer immunotherapeutic. Although the potential roles of these two enzymes in various immune cells have been broadly reported, the specific activity of PTPN2 in regulating macrophage immune and metabolic responses has yet to be fully elucidated. Hence, we sought to investigate the function of PTPN2 in macrophage polarization and on their activities. We used two different mouse models to systematically and specifically inhibit the expression of PTPN2 in macrophages and utilized a chemical inhibitor with a macrophage human cell line to assess their immune and metabolic profiles. We demonstrated that PTPN2 ablation in macrophages alters their immunometabolic transcriptome and enhances their proinflammatory response, as observed by increased IFN-ɣ and nitric oxide production. PTPN2 deficiency also leads to a dysregulation of mitochondrial respiration, as observed by decreased oxygen consumption and ATP production. We establish herein that PTPN2 dampens the proinflammatory response of macrophages while altering their mitochondrial respiration, validating its macrophage inhibition as a contributing factor in the potency of systemic dual inhibition of PTPN1 and PTPN2 against cancer.

摘要

蛋白酪氨酸磷酸酶N2(也称为TC-PTP)编码PTPN2,它是细胞因子信号传导和巨噬细胞分化的负调节因子。在过去十年中,我们以及其他一些研究团队,包括几家制药公司的工作都强调,抑制PTPN2和PTPN1(也称为PTP1B)可能成为一种新型的一流癌症免疫疗法。尽管这两种酶在各种免疫细胞中的潜在作用已有广泛报道,但PTPN2在调节巨噬细胞免疫和代谢反应中的具体活性尚未完全阐明。因此,我们试图研究PTPN2在巨噬细胞极化及其活性方面的功能。我们使用两种不同的小鼠模型来系统地、特异性地抑制巨噬细胞中PTPN2的表达,并利用一种针对巨噬细胞人细胞系的化学抑制剂来评估它们的免疫和代谢谱。我们证明,巨噬细胞中PTPN2的缺失会改变其免疫代谢转录组,并增强其促炎反应,这可通过增加IFN-γ和一氧化氮的产生来观察到。PTPN2缺乏还会导致线粒体呼吸失调,这可通过氧气消耗和ATP产生的减少来观察到。我们在此确定,PTPN2在改变巨噬细胞线粒体呼吸的同时,会抑制其促炎反应,证实其对巨噬细胞的抑制作用是PTPN1和PTPN2对癌症进行全身双重抑制效力的一个促成因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d26/12063717/8e5b68d97bcd/FSB2-39-e70536-g006.jpg

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