Sialic acid has putative signaling roles in muscle disorders of aging

唾液酸在衰老肌肉疾病中具有假定的信号作用

• 批准号: 8513221
• 负责人: Nam Pham
• 金额: $ 2.98万
• 依托单位: UT SOUTHWESTERN MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-01 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8513221
• 关键词: Affect; Age; Age-Years; Aging; Anabolism; Antibodies; Atrophic; Binding; Biopsy; Birth; Carbohydrates; Cell Communication; Cell Fractionation; Cell Nucleus; Cell surface; Cells; Cholesterol; Commit; Cytidine Monophosphate N-Acetylneuraminic Acid; Dependence; Development; Disease; Distal; Dystroglycan; Embryo; Enzymes; Eukaryota; Fatty Acids; Gene Chips; Gene Silencing; Genes; Genetic Transcription; Glycoconjugates; Glycoproteins; Homeostasis; Human; Immune system; In Vitro; Inclusion Bodies; Inclusion Body Myositis; Individual; Infiltration; Inflammatory; Inherited; Knowledge; Lead; Life; MEKs; Messenger RNA; Metabolism; Mus; Muscle; Muscle Weakness; Mutation; Myopathy; N-acetylmannosamine; Nature; Neural Cell Adhesion Molecules; Nuclear; Pathogenesis; Pathologic; Pathology; Pathway interactions; Patients; Phosphotransferases; Polysaccharides; Process; Property; Proteins; Resistance; Role; Sialic Acids; Signal Transduction; Signaling Molecule; Site; Sporadic Inclusion Body Myopathy; Time; UDP-N-acetylglucosamine 2-epimerase; Vacuole; Western Blotting; Wheelchairs; Work; analog; axonal guidance; base; combat; effective therapy; insight; muscle degeneration; mutant; new therapeutic target; novel; protein aggregate; research study; sensor; sialylation; small hairpin RNA; sugar; sugar nucleotide

DESCRIPTION (provided by applicant): Sporadic inclusion body myositis (sIBM) is the most common acquired muscle disease associated with aging. sIBM afflicts individuals older than 50 years of age. While muscle weakness develops gradually, the disease is relentlessly progressive, leading to gross atrophy and severe weakness of both the distal and proximal muscles. Afflicted individuals are wheelchair bound within 5-10 years of onset. Pathologic analyses of patient muscle biopsies reveal two pathologies: (1) infiltration of inflammatory cells and (2) muscle degenerative changes consisting of rimmed vacuole formation, protein aggregate inclusions, and myonuclear breakdown. Despite this knowledge, the exact pathogenic cascade that leads to muscle degeneration and muscle weakness is poorly understood. Furthermore, the relationship between the inflammatory and degenerative components of sIBM remains a mystery. As a result, no effective treatment for sIBM exists. Dysregulation of sialic acid biosynthesis is implicated in inclusion body myopathy (IBM) pathogenesis. Mutations in UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE), which encodes the enzyme that catalyzes the first committed step of sialic acid biosynthesis, have been found in patients suffering from hereditary inclusion body myopathy (hIBM), an autosomal recesive disease. The pathology of hIBM mimics sIBM. Additionally, like sIBM, hIBM is a disease of aging; despite having a mutant gene at birth, humans harboring hIBM mutations in GNE do not develop muscle weakness until they reach a certain age, typically their mid-20s. Understanding how mutations in GNE and subsequent disruption of sialic acid homeostasis affects transcriptional and signaling networks will provide insight into pathways dysregulated in IBM. Aim 1 of this proposal is to ascertain the ability of sialic acid to act as a signaling molecule. This will reveal pathways dysregulated in IBM muscle. Aim 2 is to determine the sialic acid metabolite(s) that is acting as a signaling molecule and to discover the protein that is acting as a sialic acid sensor. The results of this work will reveal new therapeutic targets for IBM disease. The purpose of aim 3 is to determine the dependence of sialic acid signaling on subcellular localization. Taken together, these experiments will reveal novel roles for sugar metabolism and provide mechanistic insight into IBM, a common, devastating disease.

描述（由申请人提供）：散发包涵体肌炎（sIBM）是最常见的与衰老相关的获得性肌肉疾病。sIBM折磨50岁以上的人。虽然肌肉无力是逐渐发展的，但疾病是无情的进展，导致远端和近端肌肉的严重萎缩和严重无力。患者发病后5-10年内必须坐轮椅。患者肌肉活检的病理分析显示两种病理：(1)炎症细胞浸润；(2)肌肉退行性改变，包括边缘液泡形成、蛋白质聚集包涵体和肌核破裂。尽管有这些知识，导致肌肉退化和肌肉无力的确切致病级联尚不清楚。此外，sIBM的炎症和退行性成分之间的关系仍然是一个谜。因此，目前还没有有效的sIBM治疗方法。唾液酸生物合成失调与包涵体肌病（IBM）的发病机制有关。编码唾液酸生物合成第一步的酶的udp - n -乙酰氨基葡萄糖-2- epimase / n -乙酰氨基甘露胺激酶基因（GNE）在遗传性包涵体肌病（hIBM）患者中发现突变，这是一种常染色体隐性疾病。hIBM的病理与sIBM相似。此外，与sIBM一样，hIBM也是一种衰老疾病；尽管在出生时就有突变基因，但在GNE中携带hIBM突变的人在达到一定年龄（通常是25岁左右）之前不会出现肌肉无力。了解GNE突变和随后唾液酸稳态的破坏如何影响转录和信号网络，将有助于深入了解IBM中失调的途径。本研究的目的1是确定唾液酸作为信号分子的能力。这将揭示IBM肌中失调的通路。目的2是确定作为信号分子的唾液酸代谢物，并发现作为唾液酸传感器的蛋白质。这项工作的结果将揭示IBM病的新治疗靶点。目的3是确定唾液酸信号传导对亚细胞定位的依赖性。综上所述，这些实验将揭示糖代谢的新作用，并为IBM这种常见的毁灭性疾病提供机制上的洞察。