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神经节苷脂耗竭增强小鼠关节软骨修复

Depletion of Gangliosides Enhances Articular Cartilage Repair in Mice.

机构信息

Department of Orthopaedic Surgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

Laboratory of Biochemistry, Azabu University, Graduate School of Veterinary Medicine, Sagamihara, Japan.

出版信息

Sci Rep. 2017 Mar 2;7:43729. doi: 10.1038/srep43729.

Abstract

Elucidation of the healing mechanisms in damaged tissues is a critical step for establishing breakthroughs in tissue engineering. Articular cartilage is clinically one of the most successful tissues to be repaired with regenerative medicine because of its homogeneous extracellular matrix and few cell types. However, we only poorly understand cartilage repair mechanisms, and hence, regenerated cartilage remains inferior to the native tissues. Here, we show that glycosylation is an important process for hypertrophic differentiation during articular cartilage repair. GM3, which is a precursor molecule for most gangliosides, was transiently expressed in surrounding damaged tissue, and depletion of GM3 synthase enhanced cartilage repair. Gangliosides also regulated chondrocyte hypertrophy via the Indian hedgehog pathway. These results identify a novel mechanism of cartilage healing through chondrocyte hypertrophy that is regulated by glycosylation. Manipulation of gangliosides and their synthases may have beneficial effects on articular cartilage repair.

摘要

阐明受损组织中的愈合机制是在组织工程学中取得突破的关键步骤。关节软骨是临床中应用再生医学修复最成功的组织之一,这是因为其具有同质的细胞外基质和较少的细胞类型。然而,我们对软骨修复机制的了解甚少,因此,再生的软骨仍然不如天然组织。在这里,我们表明糖基化是关节软骨修复过程中肥大分化的一个重要过程。GM3 是大多数神经节苷脂的前体分子,在周围受损组织中短暂表达,GM3 合酶的耗竭增强了软骨修复。神经节苷脂还通过印度刺猬途径调节软骨细胞肥大。这些结果确定了通过糖基化调节的软骨细胞肥大的软骨愈合的新机制。神经节苷脂及其合酶的操纵可能对关节软骨修复具有有益的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a12/5333092/f498e942f74e/srep43729-f1.jpg

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