Boileau C, Poirier F, Pelletier J-P, Guévremont M, Duval N, Martel-Pelletier J, Reboul P
Unité de Recherche en Arthrose, CR-CHUM, local Y2604, 1560 rue Sherbrooke Est, Montréal, Québec, Canada.
Ann Rheum Dis. 2008 Feb;67(2):175-81. doi: 10.1136/ard.2006.066514. Epub 2007 Jun 1.
Although galectin-3 (gal-3) is expressed during arthritic disorders, the part it plays has never been described. The aim of the study was to determine the intracellular roles of gal-3 in chondrocytes and cartilage.
Following treatment with sodium nitroprusside, a cell death inducer, intracellular levels of total and phosphorylated gal-3 were measured by immunoblots in human osteoarthritic (OA) chondrocytes. Cell viability was also assessed by the lactate dehydrogenase activity in conditioned media from OA chondrocytes or from ATDC5 cells transfected with a gal-3-expressing vector. After generating an OA model by intra-articular injection of 0.5% mono-iodoacetate (MIA), histological evaluation of articular cartilage and subchondral bone was performed in wild-type (WT) and gal-3 knockout (KO) mice aged 6 weeks and 4 months.
In vitro experiments demonstrated that intracellular gal-3 had a protective role in chondrocyte survival, which involved its phosphorylation. In contrast to 6-week-old mice, 4-month-old gal-3 KO mice, compared with WT mice, presented OA-like cartilage modifications. OA induction via MIA injection in WT mice generated cartilage lesions similar to those found in gal-3 KO animals. Moreover, OA induction showed a significant decrease in subchondral bone surface in the gal-3 KO mice in contrast to the WT group.
Altogether these findings indicate that intracellular gal-3 has a beneficial effect in articular cells, as its absence in KO mice led to cartilage lesions.
尽管半乳糖凝集素-3(gal-3)在关节炎疾病中表达,但它所起的作用从未被描述过。本研究的目的是确定gal-3在软骨细胞和软骨中的细胞内作用。
在用细胞死亡诱导剂硝普钠处理后,通过免疫印迹法测定人骨关节炎(OA)软骨细胞中总gal-3和磷酸化gal-3的细胞内水平。还通过OA软骨细胞或转染了gal-3表达载体的ATDC5细胞的条件培养基中的乳酸脱氢酶活性来评估细胞活力。通过关节内注射0.5%单碘乙酸(MIA)建立OA模型后,对6周龄和4月龄的野生型(WT)和gal-3基因敲除(KO)小鼠的关节软骨和软骨下骨进行组织学评估。
体外实验表明,细胞内gal-3对软骨细胞存活具有保护作用,这涉及到它的磷酸化。与6周龄小鼠相比,4月龄的gal-3 KO小鼠与WT小鼠相比呈现出类似OA的软骨改变。通过向WT小鼠注射MIA诱导OA产生的软骨损伤与在gal-3 KO动物中发现的损伤相似。此外,与WT组相比,OA诱导显示gal-3 KO小鼠的软骨下骨表面显著减少。
总之,这些发现表明细胞内gal-3对关节细胞具有有益作用,因为在KO小鼠中缺乏gal-3会导致软骨损伤。