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

被引:39
作者
Toegel, Stefan [1 ]
Bieder, Daniela [1 ]
Andre, Sabine [2 ]
Altmann, Friedrich [3 ]
Walzer, Sonja M. [1 ]
Kaltner, Herbert [2 ]
Hofstaetter, Jochen G. [1 ,4 ]
Windhager, Reinhard [1 ]
Gabius, Hans-Joachim [2 ]
机构
[1] Med Univ Vienna, Dept Orthopaed, Karl Chiari Lab Orthopaed Biol, A-1090 Vienna, Austria
[2] Univ Munich, Fac Vet Med, Inst Physiol Chem, Munich, Germany
[3] Univ Nat Resources & Life Sci, Dept Chem, Vienna, Austria
[4] Orthopaed Hosp Vienna Speising, Dept 2, Vienna, Austria
关键词
ARTICULAR-CARTILAGE; N-GLYCANS; GALECTIN-1; EXPRESSION; MOLECULAR SWITCHES; O-GLYCOSYLATION; DOWN-REGULATION; CROSS-LINKING; IN-VITRO; BINDING; CARCINOMA;
D O I
10.1186/ar4330
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
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 beta-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.
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页数:12
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