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Matrix reboot: IL-17 signals CAFs to create a second tumor T cell checkpoint 基质重启:IL-17信号CAFs创建第二个肿瘤T细胞检查点
Pub Date : 2022-05-18 DOI: 10.1084/jem.20220444
M. McGeachy
IL-17 promotes collagen deposition by cancer-associated fibroblasts and enhances immune exclusion of tumors.
IL-17促进癌症相关成纤维细胞的胶原沉积,增强肿瘤的免疫排斥。
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引用次数: 0
ATP spreads inflammation to other limbs through crosstalk between sensory neurons and interneurons ATP通过感觉神经元和中间神经元之间的串扰将炎症传播到其他肢体
Pub Date : 2022-05-17 DOI: 10.1084/jem.20212019
R. Hasebe, K. Murakami, Masaya Harada, N. Halaka, H. Nakagawa, F. Kawano, Y. Ohira, T. Kawamoto, F. Yull, T. Blackwell, J. Nio-Kobayashi, Toshihiko Iwanaga, Masahiko Watanabe, N. Watanabe, H. Hotta, T. Yamashita, D. Kamimura, Yuki Tanaka, M. Murakami
Local inflammation spreads to remote positions via sensory neuron–interneuron crosstalk using ATP. This neural pathway, or remote inflammation gateway reflex, may be a therapeutic target for inflammatory diseases with remote inflammation, such as rheumatoid arthritis.
局部炎症通过ATP通过感觉神经元-神经元间串扰向远处扩散。这种神经通路,或远端炎症通道反射,可能是具有远端炎症的炎症性疾病,如类风湿关节炎的治疗靶点。
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引用次数: 8
GIMAP6 regulates autophagy, immune competence, and inflammation in mice and humans GIMAP6调节小鼠和人的自噬、免疫能力和炎症
Pub Date : 2022-05-13 DOI: 10.1084/jem.20201405
Yikun Yao, Ping Du Jiang, B. Chao, D. Çağdaş, S. Kubo, Arasu Balasubramaniyam, Yu Zhang, B. Shadur, A. NaserEddin, L. Folio, Benjamin Schwarz, Eric Bohrnsen, Lixin Zheng, Matthew Lynberg, Simone Gottlieb, Michael A. Leney-Greene, Ann Y. Park, I. Tezcan, A. Akdoğan, R. Gocmen, S. Onder, A. Rosenberg, E. Soilleux, Errin Johnson, P. Jackson, J. Demeter, Samuel D. Chauvin, F. Paul, M. Selbach, H. Bulut, M. Clatworthy, Z. Tuong, Hanlin Zhang, B. Stewart, C. Bosio, P. Stepensky, S. Clare, S. Ganesan, J. Pascall, O. Daumke, G. Butcher, A. McMichael, A. Simon, M. Lenardo
Yao et al. describe GIMAP6 deficiency in humans and mice showing immune dysfunction and susceptibility to bacterial infections. They find impaired autophagy in GIMAP6-deficient immune cells and define a functional complex composed of GIMAP6, GIMAP7, and GABARAPL2.
Yao等人描述了人类和小鼠的GIMAP6缺乏,表现出免疫功能障碍和对细菌感染的易感性。他们在GIMAP6缺陷的免疫细胞中发现了受损的自噬,并定义了一个由GIMAP6、GIMAP7和GABARAPL2组成的功能复合物。
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引用次数: 3
Role of adipose tissue macrophages in obesity-related disorders 脂肪组织巨噬细胞在肥胖相关疾病中的作用
Pub Date : 2022-05-11 DOI: 10.1084/jem.20211948
S. Chakarov, Camille Blériot, F. Ginhoux
As the first immune cells to colonize tissues and long-lived resident cells, macrophages play important roles in tissue functions during early development, homeostasis, and disease. Here, Chakarov et al. discuss macrophage origin and functions in adipose tissue and how these features are modulated in obesity.
巨噬细胞作为最早在组织中定植的免疫细胞和长寿的常驻细胞,在早期发育、体内平衡和疾病的组织功能中发挥着重要作用。在这里,Chakarov等人讨论了巨噬细胞在脂肪组织中的起源和功能,以及这些特征如何在肥胖中被调节。
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引用次数: 22
Sex biases in infectious diseases research 传染病研究中的性别偏见
Pub Date : 2022-05-05 DOI: 10.1084/jem.20211486
S. Dhakal, Sabal Chaulagain, S. Klein
Reporting the distribution and inclusion of both males and females in immunology and infectious diseases research is improving, but rigorous analyses of differential outcomes between males and females, including mechanistic inquiries into the causes of sex differences, still lags behind.
关于男性和女性在免疫学和传染病研究中的分布和纳入情况的报告正在改善,但是对男性和女性之间差异结果的严格分析,包括对性别差异原因的机械调查,仍然落后。
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引用次数: 5
Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation 在高尔基体中捕获CDC42 c末端变异体驱动pyrin炎性体过度活化
Pub Date : 2022-04-28 DOI: 10.1084/jem.20211889
Masahiko Nishitani-Isa, Kojiro Mukai, Y. Honda, H. Nihira, Takayuki Tanaka, H. Shibata, K. Kodama, E. Hiejima, K. Izawa, Yuri Kawasaki, M. Osawa, Yu Katata, Sachiko Onodera, Tatsuya Watanabe, T. Uchida, S. Kure, J. Takita, O. Ohara, M. Saito, R. Nishikomori, T. Taguchi, Y. Sasahara, T. Yasumi
Using induced pluripotent stem cells carrying CDC42R186C, trapping of CDC42 C-terminal variants within the Golgi apparatus is shown to trigger autoinflammation by promoting pyrin inflammasome assembly through a mechanism independent of their GTPase activity.
利用携带CDC42R186C的诱导多能干细胞,在高尔基体中捕获CDC42 c端变体,通过一种独立于GTPase活性的机制,促进pyrin炎性体的组装,从而引发自身炎症。
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引用次数: 10
EP3 enhances adhesion and cytotoxicity of NK cells toward hepatic stellate cells in a murine liver fibrosis model EP3增强小鼠肝纤维化模型中NK细胞对肝星状细胞的粘附和细胞毒性
Pub Date : 2022-04-14 DOI: 10.1084/jem.20212414
Xixi Tao, Rui Zhang, Ronglu Du, Tingting Yu, H. Yang, Jiwen Li, Yuhong Wang, Qian Liu, Shengkai Zuo, Xi Wang, M. Lazarus, Lu Zhou, Bangmao Wang, Yingjia Yu, Yujun Shen
Tao et al. describe that activation of E-prostanoid 3 receptor (EP3) ameliorates injury-induced liver fibrosis through promoting NK cell adhesion and killing of activated hepatic stellate cells in mice, indicating that EP3 may serve as a potential therapeutic target for liver fibrosis.
Tao等人描述了E-prostanoid 3受体(EP3)的激活通过促进NK细胞粘附和杀死小鼠活化的肝星状细胞来改善损伤性肝纤维化,这表明EP3可能是肝纤维化的潜在治疗靶点。
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引用次数: 9
Toward an understanding of allogeneic conflict in pregnancy and transplantation 对妊娠和移植中同种异体冲突的理解
Pub Date : 2022-04-13 DOI: 10.1084/jem.20211493
Samarth S Durgam, M. Alegre, A. Chong
Discussion on the divergent immunological effects of pregnancy on T cell and humoral immunity, how prior pregnancy impacts responses upon alloantigen re-encounter in the context of solid organ transplantation, and potential strategies for controlling pregnancy-dependent allosensitization.
讨论妊娠对T细胞和体液免疫的不同免疫作用,既往妊娠如何影响实体器官移植中同种异体抗原再次相遇的反应,以及控制妊娠依赖性同种异体致敏的潜在策略。
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引用次数: 7
Calcium burns beige 钙烧米色
Pub Date : 2022-04-12 DOI: 10.1084/jem.20220382
Jakub Bunk, L. Kazak
In this issue of Journal of Experimental Medicine, Yin et al. (2022) discover that loss of FNIP1 is associated with browning of white adipose tissue, which they propose is driven by decreased calcium uptake into the ER.
在这一期的《实验医学杂志》上,Yin等人(2022)发现FNIP1的缺失与白色脂肪组织的褐变有关,他们认为这是由内质网钙摄取减少引起的。
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引用次数: 1
FNIP1 regulates adipocyte browning and systemic glucose homeostasis in mice by shaping intracellular calcium dynamics FNIP1通过塑造细胞内钙动力学调节小鼠脂肪细胞褐变和全身葡萄糖稳态
Pub Date : 2022-04-12 DOI: 10.1084/jem.20212491
Yujing Yin, Dengqiu Xu, Yan Mao, Liwei Xiao, Zongchao Sun, Jing Liu, Danxia Zhou, Zhisheng Xu, Lin Liu, Tingting Fu, Chenyun Ding, Qiqi Guo, Wanping Sun, Zheng Zhou, Likun Yang, Yuhuan Jia, Xinyi Chen, Z. Gan
Metabolically beneficial beige adipocytes offer tremendous potential to treat obesity and metabolic diseases. Yin et al. show that FNIP1 acts as a negative regulator of beige adipocyte thermogenesis to control systemic glucose homeostasis through modulating the ER Ca2+-ATPase SERCA.
有益代谢的米色脂肪细胞为治疗肥胖和代谢疾病提供了巨大的潜力。Yin等人的研究表明,FNIP1作为米色脂肪细胞产热的负调节因子,通过调节ER Ca2+- atp酶SERCA来控制全身葡萄糖稳态。
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引用次数: 6
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The Tokushima journal of experimental medicine
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