Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, 10833 Le Conte Ave., CHS 14-127, Los Angeles, CA 90095, USA.
Department of Microbiology, Immunology and Molecular Genetics, University of California Los Angeles, 609 Charles E Young Dr E, Los Angeles, CA 90095, USA.
Glycobiology. 2017 Dec 1;27(12):1134-1143. doi: 10.1093/glycob/cwx073.
Our understanding of muscle glycosylation to date has derived from studies in mouse models and a limited number of human lectin histochemistry studies. As various therapeutic approaches aimed at treating patients with muscular dystrophies are being translated from rodent models to human, it is critical to better understand human muscle glycosylation and relevant disease-specific differences between healthy and dystrophic muscle. Here, we report the first quantitative characterization of human muscle glycosylation, and identify differentiation- and disease-specific differences in human muscle glycosylation. Utilizing a panel of 13 lectins with varying glycan specificities, we surveyed lectin binding to primary and immortalized myoblasts and myotubes from healthy and dystrophic sources. Following differentiation of primary and immortalized healthy human muscle cells, we observed increased binding of Narcissus pseudonarcissus agglutinin (NPA), PNA, MAA-II and WFA to myotubes compared to myoblasts. Following differentiation of immortalized healthy and dystrophic human muscle cells, we observed disease-specific differences in binding of NPA, Jac and Tricosanthes japonica agglutinin-I (TJA-I) to differentiated myotubes. We also observed differentiation- and disease-specific differences in binding of NPA, Jac, PNA, TJA-I and WFA to glycoprotein receptors in muscle cells. Additionally, Jac, PNA and WFA precipitated functionally glycosylated α-DG, that bound laminin, while NPA and TJA-I did not. Lectin histochemistry of healthy and dystrophic human muscle sections identified disease-specific differences in binding of O-glycan and sialic acid-specific lectins between healthy and dystrophic muscle. These results indicate that specific and discrete changes in glycosylation occur following differentiation, and identify specific lectins as potential biomarkers sensitive to changes in healthy human muscle glycosylation.
迄今为止,我们对肌肉糖基化的认识主要来源于小鼠模型和少数人类凝集素组织化学研究。由于各种旨在治疗肌肉营养不良症患者的治疗方法正从啮齿动物模型转化为人类,因此更好地了解人类肌肉糖基化以及健康和病变肌肉之间的相关疾病特异性差异至关重要。在这里,我们首次对人类肌肉糖基化进行了定量描述,并确定了人类肌肉糖基化的分化和疾病特异性差异。利用一组具有不同聚糖特异性的 13 种凝集素,我们调查了凝集素与来自健康和病变来源的原代和永生化成肌细胞及肌管的结合情况。在原代和永生化健康人类肌肉细胞分化后,与成肌细胞相比,我们观察到水仙花凝集素(NPA)、PNA、MAA-II 和 WFA 对肌管的结合增加。在永生化健康和病变人类肌肉细胞分化后,我们观察到 NPA、Jac 和三叶猪殃殃凝集素-I(TJA-I)与分化的肌管结合存在疾病特异性差异。我们还观察到 NPA、Jac、PNA、TJA-I 和 WFA 与肌肉细胞中糖蛋白受体的结合存在分化和疾病特异性差异。此外,Jac、PNA 和 WFA 沉淀了功能糖基化的α-DG,其与层粘连蛋白结合,而 NPA 和 TJA-I 则没有。健康和病变人类肌肉切片的凝集素组织化学鉴定出健康和病变肌肉之间 O-聚糖和唾液酸特异性凝集素结合的疾病特异性差异。这些结果表明,在分化后会发生特定和离散的糖基化变化,并确定特定的凝集素作为潜在的生物标志物,对健康人类肌肉糖基化的变化敏感。