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ATP in the mechanotransduction pathway of normal human chondrocytes

机译:正常人软骨细胞机械转导途径中的ATP

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on chondrocyte function, generally acting via P2 purinoceptors. We have previously shown that mechanical stimulation at 0.33 Hz of normal human chondrocyte cultures causes cellular hyperpolarisation, while chondrocytes derived from osteoarthritic (OA) cartilage depolarise. Experiments have been undertaken to establish whether ATP is involved in the response of the chondrocyte to mechanical stimulation. Chondrocytes, isolated from normal and OA cartilage obtained, with consent, from human knee joints following surgery, were cultured in non-confluent monolayer. Cells were mechanically stimulated at 0.33 Hz for 20 minutes at 37℃ in the presence or absence of inhibitors of ATP signalling, or were stimulated by the addition of exogenous ATP or derivatives, and electrophysiological measurements recorded. Samples of medium bathing the cells were collected before and after mechanical stimulation, and the concentration of ATP in the cell medium was measured. Total RNA was extracted from cultured chondrocytes, reverse-transcribed and used for RT-PCR with primers specific for P2Y2 purinoceptors. ATP, UTP 2-methylthioadenosine and α/β-methylene adenosine 5′-triphosphate all induced a hyperpolarisation response in normal human articular chondrocytes. No significant change was observed in the membrane potentials of chondrocytes isolated from OA cartilage following the addition of these nucleotides to the medium. In normal chondrocytes, the hyperpolarisation induced by ATP was blocked by the presence of apamin, indicating the involvement of small-conductance calcium-activated potassium channels. Following mechanical stimulation of normal ehondrocytes, an increase was observed in ATP concentration in the cell culture medium bathing the cells. The presence within the culture medium of suramin or pyridoxal-phosphate-6-azophenyl-2′, 4′-disulphonic acid (PPADS) prior to and during the period of mechanical stimulation abolished the hyperpolarisation response in normal chondrocytes. The presence of mRNA for P2Y2 purinoceptors was demonstrated in both normal and OA chondrocytes by RT-PCR. These results suggest that ATP has a role in the response of normal chondrocytes to mechanical stimulation, via P2Y2 purinoceptors. This response appears to be different in chondrocytes derived from OA cartilage, and may be important in the progression of this disease.
机译:通常通过P2嘌呤受体起作用。先前我们已经证明,正常人软骨细胞培养物在0.33 Hz的机械刺激会导致细胞超极化,而源自骨关节炎(OA)软骨的软骨细胞会去极化。已经进行实验以确定ATP是否参与软骨细胞对机械刺激的反应。在同意后,从人膝关节分离自正常和OA软骨分离的软骨细胞,在非融合单层中培养。在存在或不存在ATP信号抑制剂的情况下,在0.33 Hz下于37℃机械刺激细胞20分钟,或通过添加外源ATP或衍生物刺激细胞,并记录电生理学测量值。在机械刺激之前和之后收集浸没细胞的培养基样品,并测量细胞培养基中ATP的浓度。从培养的软骨细胞中提取总RNA,逆转录后,用对P2Y2嘌呤受体特异的引物进行RT-PCR。 ATP,UTP 2-甲基硫代腺苷和α/β-亚甲基腺苷5'-三磷酸酯均在正常人关节软骨细胞中诱导超极化反应。将这些核苷酸添加到培养基中后,从OA软骨分离的软骨细胞的膜电位未见明显变化。在正常的软骨细胞中,由ATP诱导的超极化被罂粟碱的存在所阻止,表明参与了小传导钙激活的钾通道。机械刺激正常的母细胞后,在浸泡细胞的细胞培养基中观察到ATP浓度增加。在机械刺激之前和期间,苏拉明或吡ido醛-磷酸-6-偶氮苯基-2',4'-二磺酸(PPADS)在培养基中的存在消除了正常软骨细胞中的超极化反应。通过RT-PCR在正常和OA软骨细胞中证明了P2Y2嘌呤受体的mRNA的存在。这些结果表明,ATP通过P2Y2嘌呤受体在正常软骨细胞对机械刺激的反应中起作用。这种反应在源自OA软骨的软骨细胞中似乎是不同的,并且在该疾病的进展中可能是重要的。

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