Department of Mechanical Engineering, University of Delaware, Newark, Delaware, USA.
Center for Bioinformatics and Computational Biology, University of Delaware, Newark, Delaware, USA.
FASEB J. 2019 Apr;33(4):4675-4687. doi: 10.1096/fj.201801460R. Epub 2019 Jan 2.
Intracellular calcium ([Ca]) oscillation is a fundamental signaling response of cartilage cells under mechanical loading or osmotic stress. Chondrocytes are usually considered as nonexcitable cells with no spontaneous [Ca] signaling. This study proved that chondrocytes can exhibit robust spontaneous [Ca] signaling without explicit external stimuli. The intensity of [Ca] peaks from individual chondrocytes maintain a consistent spatiotemporal pattern, acting as a unique "fingerprint" for each cell. Statistical analysis revealed lognormal distributions of the temporal parameters of [Ca] peaks, as well as strong linear correlations between their means and sds. Based on these statistical findings, we hypothesized that the spontaneous [Ca] peaks may result from an autocatalytic process and that [Ca] oscillation is controlled by a threshold-regulating mechanism. To test these 2 mechanisms, we established a multistage biophysical model by assuming the spontaneous [Ca] signaling of chondrocytes as a combination of deterministic and stochastic processes. The theoretical model successfully explained the lognormal distribution of the temporal parameters and the fingerprint feature of [Ca] peaks. In addition, by using antagonists for 10 pathways, we revealed that the initiation of spontaneous [Ca] peaks in chondrocytes requires the presence of extracellular Ca, and that the PLC-inositol 1,4,5-trisphosphate pathway, which controls the release of calcium from the endoplasmic reticulum, can affect the initiation of spontaneous [Ca] peaks in chondrocytes. The purinoceptors and transient receptor potential vanilloid 4 channels on the plasma membrane also play key roles in the spontaneous [Ca] signaling of chondrocytes. In contrast, blocking the T-type or L-type voltage-gated calcium channel promoted the spontaneous calcium signaling. This study represents a systematic effort to understand the features and initiation mechanisms of spontaneous [Ca] signaling in chondrocytes, which are critical for chondrocyte mechanobiology.-Zhou, Y., Lv, M., Li, T., Zhang, T., Duncan, R., Wang, L., Lu, X. L. Spontaneous calcium signaling of cartilage cells: from spatiotemporal features to biophysical modeling.
细胞内钙 ([Ca]) 振荡是软骨细胞在机械加载或渗透胁迫下的基本信号响应。软骨细胞通常被认为是无兴奋细胞,没有自发的 [Ca] 信号。本研究证明软骨细胞在没有明确外部刺激的情况下可以表现出强烈的自发 [Ca] 信号。单个软骨细胞的 [Ca] 峰强度保持一致的时空模式,作为每个细胞的独特“指纹”。统计分析显示 [Ca] 峰的时间参数呈对数正态分布,其均值和标准差之间也存在很强的线性相关性。基于这些统计发现,我们假设自发 [Ca] 峰可能是自催化过程的结果,[Ca] 振荡受阈值调节机制控制。为了验证这 2 种机制,我们假设软骨细胞的自发 [Ca] 信号是确定性和随机性过程的组合,建立了一个多阶段的生物物理模型。理论模型成功解释了时间参数的对数正态分布和 [Ca] 峰的指纹特征。此外,通过使用 10 种途径的拮抗剂,我们揭示了细胞外 Ca 的存在对于软骨细胞中自发 [Ca] 峰的起始是必需的,并且质膜上的 PLC-肌醇 1,4,5-三磷酸途径可以控制内质网中钙的释放,从而影响软骨细胞中自发 [Ca] 峰的起始。质膜上的嘌呤能受体和瞬时受体电位香草醛 4 通道在软骨细胞的自发 [Ca] 信号中也起着关键作用。相反,阻断 T 型或 L 型电压门控钙通道促进了自发钙信号。本研究代表了理解软骨细胞自发 [Ca] 信号特征和起始机制的系统努力,这对于软骨细胞的机械生物学至关重要。