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Effects of Adipokines and Insulin on Intracellular pH, Calcium Concentration, and Responses to Hypo-Osmolarity in Human Articular Chondrocytes from Healthy and Osteoarthritic Cartilage

机译:脂肪因子和胰岛素对健康和骨关节炎软骨细胞的pH,钙浓度和对低渗渗透压反应的影响

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Objective: To evaluate the effects of adipokines and insulin on intracellular calcium concentration ([Ca2+]i) and pH (pHi) in human articular chondrocytes from healthy (CHC) and osteoarthritic cartilage (COC). Design: pHi and [Ca2+]i were measured using BCECF and Fura-2 fluorometric probes in CHC and COC under control conditions and following a hypotonic shock. The effects of interleukin-1β (IL1β), tumor necrosis factor-α (TNFα), insulin, leptin, resistin, and adiponectin were assessed. Results: pHi was lower in COC than in CHC. Only IL1β β decreased pHi in both cell types; all the agents enhanced pHi recovery following an ammonium prepulse in CHC, effect that was attenuated by Na+–H+ exchanger inhibitors, but they had no effect in COC. Hypotonic shock (HTS) caused a pHi increase, which was significantly smaller in COC. All the hormones attenuated this response and the effect of IL1β was greater. The basal [Ca2+]i was similar in COC and CHC; IL1β, TNFα, and insulin increased the [Ca2+]i, but leptin, resistin, and adiponectin did not. These effects were greater in COC. This [Ca2+]i increase was dependent on extracellular Ca2+ and attenuated by Na+–Ca2+ exchanger inhibitors. HTS caused a [Ca2+]i increase, which was inhibited by transient receptor potential vanilloid blockers and attenuated by all the hormones tested with the exception of adiponectin. Conclusions: These findings may help explain the association between obesity and osteoarthritis, in which these hormones are altered. The responses of CHC and COC are different, which suggests that a modification of pH and Ca2+ homeostasis is part of the osteoarthritis pathophysiology.
机译:目的:评价脂肪因子和胰岛素对健康人(CHC)和骨关节炎软骨(COC)人关节软骨细胞内钙离子浓度([Ca2 +] i)和pH(pHi)的影响。设计:pHi和[Ca2 +] i是在控制条件下和低渗性休克后,在CHC和COC中使用BCECF和Fura-2荧光探针测量的。评估白介素-1β(IL1β),肿瘤坏死因子-α(TNFα),胰岛素,瘦素,抵抗素和脂联素的作用。结果:COC中的pHi低于CHC。在两种细胞类型中,只有IL1ββ降低pHi。所有试剂均可在CHC中施加氨预脉冲后提高pHi的回收率,但Na + –H +交换抑制剂会减弱这种作用,但对COC没有影响。低渗性休克(HTS)导致pHi升高,而COC显着减小。所有激素都减弱了这种反应,IL1β的作用更大。 COC和CHC中的基础[Ca2 +] i相似。 IL1β,TNFα和胰岛素增加[Ca2 +] i,但瘦素,抵抗素和脂联素则没有。这些影响在COC中更大。 [Ca2 +] i的增加取决于细胞外Ca2 +,并被Na + –Ca2 +交换抑制剂抑制。 HTS引起[Ca2 +] i的增加,这被瞬时受体电位类香草酸阻滞剂抑制,除脂连蛋白外,所有测试的激素均减弱了[Ca2 +] i。结论:这些发现可能有助于解释肥胖与骨关节炎之间的联系,其中这些激素被改变。 CHC和COC的响应不同,这表明pH和Ca2 +稳态的改变是骨关节炎病理生理学的一部分。

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