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Identification of BATF function and targets during NK cell activation

NK 细胞激活过程中 BATF 功能和靶标的鉴定

基本信息

批准号：
10354363
负责人：
BARBARA L. KEE
金额：
$ 20.5万
依托单位：
UNIVERSITY OF CHICAGO
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-09-23 至 2023-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10354363
关键词：
Activated Natural Killer Cell Address Bacteria Binding Binding Sites CD8-Positive T-Lymphocytes Cell physiology Cell surface Cells Chromatin Chronic Computer Analysis Coronavirus Cytokine Receptors Cytokine Signaling Data Disease Environment Exploratory/Developmental Grant Family Foundations Future Gene Expression Genes Genetic Transcription Germ Lines Goals Grant Herpesviridae Histocompatibility IRF4 gene Immune response Infection Inflammatory Interferon Type II Interleukin-12 Interleukin-18 Knowledge Lead Ligands Malignant - descriptor Metastatic Melanoma Metastatic to Methods Modeling Murid herpesvirus 1 Mus NK Cell Activation Natural Killer Cells Neoplasm Metastasis Pathogenicity Pathway interactions Phase Play Production Receptor Signaling Role Series Signal Pathway Signal Transduction Signaling Protein Site Solid Neoplasm Stress Testing Therapeutic Time Transcription Factor AP-1 Transcriptional Activation Viral Cancer Virus Virus Diseases XCL1 gene anti-cancer cell motility chemokine cytokine cytotoxicity immune checkpoint blockade insight melanoma member migration novel pathogen programs receptor response transcription factor transcriptome sequencing tumor tumor microenvironment

项目摘要

Project Summary Natural killer (NK) cells play essential roles in the immune response to intracellular pathogens, including viruses and bacteria, and form an important defense against malignant transformation and metastasis. NK cells are activated when they detect an imbalance in the signals from receptors on their cell surface, either a loss of inhibitory signals or activation through activating receptors including cytokine receptors. Alterations in these signaling pathways impact the transcriptional regulatory networks that contribute to NK cell activation and effector function. At the present time there is a gap in our knowledge of the major transcription factors that are impacted by these signaling pathways and how they modulate NK cell function. In this R21 application, we present data to support the hypothesis that Batf, the founding member of the AP-1 family of transcription factors, is induced by proinflammatory cytokine signaling in NK cells and impacts multiple aspects of the NK cell response. In aim 1, we will test the hypothesis that Batf regulates key genes involved in NK cell expansion, survival, and effector function by identifying direct Batf targets during the response to mouse cytomegalovirus. In aim 2, we will test the hypothesis that Batf plays unique roles in different NK cell activating contexts by testing the requirement for Batf in the NK cell response to metastatic melanoma and in a solid tumor model that relies on NK cell migration and chemokine production. Taken together, these studies will provide a broad view of the requirements for Batf in distinct NK cell activation contexts and lead to the identification of Batf targets that underlie its essential functions.

项目总结