Nonreceptor tyrosine kinases in Systemic Lupus Erythematosus

系统性红斑狼疮中的非受体酪氨酸激酶

• 批准号: 10409830
• 负责人: W Todd MILLER
• 金额: $ 31.56万
• 依托单位: STATE UNIVERSITY NEW YORK STONY BROOK
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-05-25 至 2026-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10409830
• 关键词: Active Sites; Apoptosis; Apoptotic; Autoimmune Diseases; BCAR1 gene; Binding; Binding Sites; Biological Assay; Cell Surface Receptors; Cell model; Cells; Collaborations; Coupled; Coupling; Crystallization; Disease; Environmental Risk Factor; Enzyme Kinetics; Enzymes; Eukaryotic Cell; Excision; Fluorescence; Genetic; Growth; Human; Inflammatory; Insecta; Laboratories; Light; Link; Lupus; Malignant Neoplasms; Mammalian Cell; Mammary Neoplasms; Measures; Mutation; Normal Cell; PTK6 gene; Pathology; Pathway interactions; Patients; Phagocytes; Phagocytosis; Phosphatidylserines; Phosphotransferases; Physiological; Physiology; Protein Tyrosine Kinase; Proteins; Receptor Protein-Tyrosine Kinases; Regulation; Role; Series; Signal Pathway; Signal Transduction; Structure; Substrate Specificity; Systemic Lupus Erythematosus; Testing; Work; cohort; experimental study; human disease; induced pluripotent stem cell; insight; loss of function mutation; macrophage; mutant; new therapeutic target; novel; novel therapeutic intervention; three dimensional structure

Tyrosine kinases are important regulators of growth, differentiation, and apoptosis in eukaryotic cells. Inappropriate tyrosine kinase signaling is observed in many cancers and inflammatory diseases. This project focuses on the structure, activity, and regulation of the Ack1 and Brk nonreceptor tyrosine kinases. In collaboration with Dr. Frederic Geissmann and colleagues, we have discovered a series of loss-of- function mutations in Ack1 and Brk in a cohort of patients with severe Systemic Lupus Erythematosus (SLE). These are the first tyrosine kinase mutations found to be linked to this disease. Our preliminary work shows that the mutations drastically decrease (or completely block) kinase activity, downstream signaling, and phagocytosis of apoptotic cells. We propose to conduct functional studies of the wild-type and mutant forms of Ack1 and Brk in mammalian cells, including experiments in induced pluripotent stem cell (iPSC)- derived macrophages from the lupus patients and their healthy relatives. We will carry out global screens of substrate specificity to determine whether the mutations “rewire” cellular signaling networks. We will also carry out mechanistic and structural studies on the purified mutant kinases, and test how they are coupled to the cell surface receptor MerTK. The overall hypothesis is that Ack1 and Brk link recognition of phosphatidylserine on apoptotic cells to phagocytic engulfment. Regulation or tuning of this signaling pathway could provide a new strategy for therapeutic approaches in autoimmune diseases.

酪氨酸激酶是真核细胞生长、分化和凋亡的重要调节因子。 在许多癌症和炎性疾病中观察到不适当的酪氨酸激酶信号传导。这 该项目的重点是结构，活动和调节的Ack 1和Brk非受体酪氨酸激酶。 在与Frederic Geissmann博士及其同事的合作中，我们发现了一系列... 一组严重系统性红斑狼疮患者中Ack 1和Brk的功能突变 （SLE）。这些是发现与这种疾病有关的第一个酪氨酸激酶突变。我们的前期工作 显示突变显著降低（或完全阻断）激酶活性，下游信号传导， 和吞噬凋亡细胞。我们建议对野生型和突变型进行功能研究 哺乳动物细胞中的Ack 1和Brk形式，包括诱导多能干细胞（iPSC）实验- 从狼疮患者及其健康亲属中提取的巨噬细胞。我们将进行全球筛查 底物特异性，以确定突变是否“重新连接”细胞信号网络。我们还将 对纯化的突变激酶进行机制和结构研究，并测试它们是如何偶联的 细胞表面受体MerTK。总的假设是，Ack 1和Brk连接识别 磷脂酰丝氨酸对凋亡细胞的吞噬作用。调节或调谐这种信号 该通路可能为自身免疫性疾病的治疗提供新的策略。