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首页> 外文期刊>The Journal of rheumatology >Avocado/soybean unsaponifiables prevent the inhibitory effect of osteoarthritic subchondral osteoblasts on aggrecan and type II collagen synthesis by chondrocytes.
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Avocado/soybean unsaponifiables prevent the inhibitory effect of osteoarthritic subchondral osteoblasts on aggrecan and type II collagen synthesis by chondrocytes.

机译:鳄梨/大豆不皂化物阻止骨关节炎软骨下成骨细胞抑制软骨聚集蛋白聚糖和II型胶原的合成。

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OBJECTIVE: To determine the effects of avocado/soybean unsaponifiables (ASU) on osteoblast-induced dysregulation of chondrocyte metabolism. METHODS: Human chondrocytes were isolated from osteoarthritis (OA) cartilage and cultured in alginate beads for 4 or 10 days in the absence or presence of osteoblasts isolated from nonsclerotic (NSC) or sclerotic (SC) zones of OA subchondral bone plate in monolayer. Before co-culture, osteoblasts were incubated or not with 10 microg/ml ASU for 72 hours. Aggrecan, type II collagen, matrix metalloproteinase-3 (MMP-3) and MMP-13, tissue inhibitor of metalloproteinase (TIMP-1), transforming growth factor-beta1 (TGF-beta1) and TGF-beta3, inducible NO synthase (iNOS), and cyclooxygenase-2 (COX-2) mRNA levels in chondrocytes were quantified by RT-PCR. Aggrecan, osteocalcin, TGF-beta1, interleukin 1beta (IL-1beta), and IL-6 production were assayed by immunoassays. RESULTS: In co-culture, SC osteoblasts induced a significant inhibition of matrix protein production and a significant increase of MMP synthesis by chondrocytes. In contrast, SC osteoblasts did not modify TIMP-1, TGF-beta1 and TGF-beta3, iNOS, or COX-2 mRNA levels in chondrocytes. The pretreatment of SC osteoblasts with ASU fully prevented the inhibitory effects of SC osteoblasts on matrix component production, and even significantly increased type II collagen mRNA level over the control (chondrocytes alone) value. In contrast, pretreatment of SC osteoblasts with ASU did not significantly modify the expression of MMP, TIMP-1, TGF-beta1, TGF-beta3, iNOS, or COX-2 gene by chondrocytes. CONCLUSION: ASU prevent the osteoarthritic osteoblast-induced inhibition of matrix molecule production, suggesting that this compound may promote OA cartilage repair by acting on subchondral bone osteoblasts. This finding constitutes a new mechanism of action for this compound, known for its beneficial effects on cartilage.
机译:目的:确定鳄梨/大豆不皂化物(ASU)对成骨细胞诱导的软骨细胞代谢失调的影响。方法:从骨关节炎(OA)软骨中分离出人类软骨细胞,并在藻酸盐珠粒中培养4或10天,不存在或存在从单层OA软骨下骨板的非硬化(NSC)或硬化(SC)区分离的成骨细胞。共培养前,将成骨细胞与否与10 microg / ml ASU孵育72小时。 Aggrecan,II型胶原蛋白,基质金属蛋白酶3(MMP-3)和MMP-13,金属蛋白酶组织抑制剂(TIMP-1),转化生长因子β1(TGF-beta1)和TGF-beta3,诱导型一氧化氮合酶(iNOS) ),并通过RT-PCR定量软骨细胞中的环氧合酶2(COX-2)mRNA水平。用免疫测定法测定了Aggrecan,骨钙蛋白,TGF-β1,白介素1β(IL-1β)和IL-6的产生。结果:在共培养中,SC成骨细胞显着抑制了基质蛋白的产生,并显着增加了软骨细胞MMP的合成。相反,SC成骨细胞没有改变软骨细胞中的TIMP-1,TGF-beta1和TGF-beta3,iNOS或COX-2 mRNA水平。用ASU预处理SC成骨细胞完全阻止了SC成骨细胞对基质成分产生的抑制作用,甚至显着提高了II型胶原mRNA水平,使其超过了对照值(仅软骨细胞)。相反,用ASU预处理SC成骨细胞不会明显改变软骨细胞的MMP,TIMP-1,TGF-beta1,TGF-beta3,iNOS或COX-2基因的表达。结论:ASU可以预防骨关节炎成骨细胞对基质分子产生的抑制作用,表明该化合物可能通过作用于软骨下成骨细胞来促进OA软骨修复。这一发现构成了该化合物的一种新的作用机理,以其对软骨的有益作用而闻名。

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