Kruppel-like factor-6 signaling in myelin formation and repair

髓磷脂形成和修复中的 Kruppel 样因子 6 信号传导

• 批准号: 8818597
• 负责人: GARETH R JOHN
• 金额: $ 37.08万
• 依托单位: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-08-15 至 2019-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8818597
• 关键词: Adult; Axon; Binding; Blindness; Cells; Chromatin; Complex; Data; Demyelinations; Disease; Epigenetic Process; Failure; Genes; Goals; In Vitro; Knowledge; Label; Lesion; Link; Morphology; Multiple Sclerosis; Mus; Myelin; Oligodendroglia; Paralysed; Pathology; Pathway interactions; Patients; Pattern; Proliferating; RXR; Recovery of Function; Recruitment Activity; Research; Role; Signal Transduction; Staging; Symptoms; Testing; Time; Transactivation; Transcription Coactivator; Work; design; genome-wide analysis; histone acetyltransferase; in vivo; myelination; novel; progenitor; programs; public health relevance; remyelination; repaired; white matter

DESCRIPTION (provided by applicant): In multiple sclerosis (MS), demyelination of axons produces conduction block and symptoms including paralysis and blindness, while myelin repair (remyelination) brings functional recovery. A key goal in MS research is to enhance remyelination, which occurs spontaneously but is inefficient, especially in the later stages of the disease. Oligodendrocyte progenitors (OLP) are the major reservoir of remyelinating cells. Their differentiation occurs via an intrinsic transcriptional program, which is promoted by extrinsic pathways, including Stat3, Smad3, Akt-PI3kinase, Erk1/2 and Tralpha1/RXR signaling. Elucidating how these pathways promote differentiation may identify new strategies to enhance remyelination. Recently, we identified the Kr�ppel-like transcriptional activator Klf6 as an essential coordinator of CNS myelination. Importantly, our data also indicate that Klf6 signaling links extrinsic pathways to the intrinsic differentiation program. Notably, key extrinsic pro-myelinating pathways (Stat3 and Smad3 signaling) strongly induce Klf6 in differentiating cells, and Klf6 over-expression accelerates differentiation. Conversely, Klf6 deletion in vitro or in vivo blocks vital steps in differentiation, and leads to complete failure of myelination. This pathology partly mimics deficits resulting from Stat3 or Smad3 inactivation. The effects of Klf6 are restricted to the differentiation program - inactivation in proliferating or mature cells produces o pathology. Our data further suggest important roles in adults, in normal myelin turnover and, critically, in remyelination. Klf6 is strongly induced in remyelinating lesions, paralleling activaion of extrinsic pro-myelinating pathways. To understand Klf6 mechanism of action, we have now used genome-wide analysis of chromatin occupancy, and transcriptional profiling. This work has identified a program of both novel and anticipated Klf6- regulated genes. Importantly, their roles propose Klf6 contributions to sequential steps in differentiation. Moreover, our data further indicate that Klf6 binding also recruits epigenetic coactivators to target loci, and that these enhance transactivation of its transcriptional targets. Together, our findings suggest that Klf6 may form complexes with transcriptional and epigenetic coactivators, to promote differentiation and myelin formation. In this proposal, we will test the central hypothesis that Klf6 linkage of extrinsic regulators with the intrinsic differentiation program is essential for CNS remyelination. We propose three Specific Aims. In Aim 1, we will test the extent to which extrinsic pro-myelinating factors promote differentiation via Klf6 signaling. In Aim 2, we will define the mechanism of action by which Klf6 controls differentiation. In Aim 3, we will then test the role of Klf6 signaling in adult white matter, in normal myelin turnover and, critically, in remyelination. This work will define a new mechanism required for myelin formation, and which may be vital for repair. Elucidating how extrinsic pathways promote maturation may identify new strategies to enhance remyelination.

描述（由申请人提供）：在多发性硬化症（MS）中，轴突脱髓鞘导致传导阻滞和麻痹、失明等症状，髓磷脂修复（髓鞘再生）带来功能恢复。多发性硬化症研究的一个关键目标是增强髓鞘再生，这种再生是自发发生的，但效率低下，特别是在多发性硬化症的后期