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通过 RT-qPCR、质谱法、植物/人凝集素的组织化学和糖蛋白的凝集素定位对骨关节炎软骨和软骨细胞进行糖表型分析。

Glycophenotyping of osteoarthritic cartilage and chondrocytes by RT-qPCR, mass spectrometry, histochemistry with plant/human lectins and lectin localization with a glycoprotein.

出版信息

Arthritis Res Ther. 2013 Oct 4;15(5):R147. doi: 10.1186/ar4330.

Abstract

INTRODUCTION

This study aimed to characterize the glycophenotype of osteoarthritic cartilage and human chondrocytes.

METHODS

Articular knee cartilage was obtained from nine osteoarthritis (OA) patients. mRNA levels for 27 glycosyltransferases were analyzed in OA chondrocytes using RT-qPCR. Additionally, N- and O-glycans were quantified using mass-spectrometry. Histologically, two cartilage areas with Mankin scores (MS) either ≤ 4 or ≥ 9 were selected from each patient representing areas of mild and severe OA, respectively. Tissue sections were stained with (1) a selected panel of plant lectins for probing into the OA glycophenotype, (2) the human lectins galectins-1 and -3, and (3) the glycoprotein asialofetuin (ASF) for visualizing β-galactoside-specific endogenous lectins.

RESULTS

We found that OA chondrocytes expressed oligomannosidic structures as well as non-, mono- and disialylated complex-type N-glycans, and core 2 O-glycans. Reflecting B4GALNT3 mRNA presence in OA chondrocytes, LacdiNAc-terminated structures were detected. Staining profiles for plant and human lectins were dependent on the grade of cartilage degeneration, and ASF-positive cells were observed in significantly higher rates in areas of severe degeneration.

CONCLUSIONS

In summary, distinct aspects of the glycome in OA cartilage are altered with progressing degeneration. In particular, the alterations measured by galectin-3 and the pan-galectin sensor ASF encourage detailed studies of galectin functionality in OA.

摘要

简介

本研究旨在描述骨关节炎软骨和人软骨细胞的糖表型。

方法

从 9 名骨关节炎(OA)患者的膝关节软骨中获取关节软骨。使用 RT-qPCR 分析 OA 软骨细胞中 27 种糖基转移酶的 mRNA 水平。此外,使用质谱法定量 N-和 O-聚糖。组织学上,从每位患者中选择两个具有曼金评分(MS)≤4 或≥9 的软骨区域,分别代表轻度和重度 OA 区域。组织切片用(1)一组选定的植物凝集素对 OA 糖表型进行探测,(2)人凝集素半乳糖凝集素-1 和 -3,以及(3)糖蛋白脱唾液酸胎球蛋白(ASF)对β-半乳糖苷特异性内源性凝集素进行可视化。

结果

我们发现 OA 软骨细胞表达寡甘露糖结构以及非、单和二唾液酸化的复杂型 N-聚糖和核心 2 O-聚糖。反映 B4GALNT3 mRNA 在 OA 软骨细胞中的存在,检测到 LacdiNAc 末端结构。植物和人凝集素的染色模式依赖于软骨退化的程度,并且在严重退化区域中观察到 ASF 阳性细胞的比例显著更高。

结论

总之,OA 软骨中糖组的不同方面随着退化的进展而改变。特别是,通过半乳糖凝集素-3 和泛半乳糖凝集素传感器 ASF 测量的改变鼓励对 OA 中半乳糖凝集素功能进行详细研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73f7/3978707/e573af7d94c9/ar4330-1.jpg

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