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正常人软骨细胞机械转导途径中的三磷酸腺苷

ATP in the mechanotransduction pathway of normal human chondrocytes.

作者信息

Millward-Sadler S J, Wright M O, Flatman P W, Salter D M

机构信息

Osteoarticular Research Group, Division of Pathology, School of Molecular and Clinical Medicine, College of Medicine and Veterinary Medicine, Edinburgh University Medical School, Teviot Place, Edinburgh, UK.

出版信息

Biorheology. 2004;41(3-4):567-75.

Abstract

Extracellular nucleotides have been shown to have diverse effects 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 degrees C 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 alphabeta-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 chondrocytes, 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.

摘要

细胞外核苷酸已被证明对软骨细胞功能有多种影响,通常通过P2嘌呤受体起作用。我们之前已经表明,以0.33Hz的频率对正常人软骨细胞培养物进行机械刺激会导致细胞超极化,而源自骨关节炎(OA)软骨的软骨细胞则会发生去极化。已经进行了实验以确定ATP是否参与软骨细胞对机械刺激的反应。从接受手术的人膝关节中获得的正常和OA软骨中分离出的软骨细胞,经同意后在非汇合单层中培养。在存在或不存在ATP信号抑制剂的情况下,将细胞在37℃下以0.33Hz机械刺激20分钟,或者通过添加外源性ATP或其衍生物进行刺激,并记录电生理测量结果。在机械刺激前后收集细胞培养液样本,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,逆转录并用于使用针对P2Y2嘌呤受体的特异性引物进行RT-PCR。ATP、UTP、2-甲硫基腺苷和αβ-亚甲基腺苷5'-三磷酸均在正常人关节软骨细胞中诱导超极化反应。向培养基中添加这些核苷酸后,未观察到从OA软骨分离的软骨细胞膜电位有明显变化。在正常软骨细胞中,ATP诱导的超极化被蜂毒肽的存在所阻断,表明小电导钙激活钾通道参与其中。对正常软骨细胞进行机械刺激后,观察到细胞培养液中ATP浓度增加。在机械刺激之前和期间,培养基中存在苏拉明或磷酸吡哆醛-6-偶氮苯基-2',4'-二磺酸(PPADS)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软骨细胞中均证明了P2Y2嘌呤受体的mRNA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有所不同,并且可能在该疾病的进展中起重要作用。

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