Vatsal Vora Hardagna, Jha Brajesh Kumar, Singh Tajinder Pal
Department of Mathematics, School of Technology, Pandit Deendayal Energy University, Gandhinagar, Gujarat, India.
Cell Biochem Biophys. 2024 Dec;82(4):3401-3411. doi: 10.1007/s12013-024-01425-3. Epub 2024 Aug 6.
Calcium ions are the second messenger playing as regulators for various cellular activities. Its spatiotemporal control is critical for various brain functions, including neuroplasticity, apoptosis, and cell death. The Endoplasmic Reticulum (ER) plays an important role in determining these spatiotemporal calcium dynamics. Stromal interaction molecule (STIM) - Orai channel on the membrane generates additional calcium flow, whereas other membrane fluxes contribute to cytosolic flux. Due to their anomalous character, we used the Caputo fractional differential operator to mimic these interactions in polar coordinates. Solutions were generated using hybrid integral transform methods to control the analytical approach. Using Green's function yielded a closed-form solution for Mittag-Leffler-type functions. This work emphasizes the significant relationship between calcium and various buffer levels in neurons. The differential transition simulation of a time derivative with space across different parameters indicated a decrease in calcium concentration. Anomalously low buffer levels exhibited the impact of Alzheimer's disease on calcium higher concentration, leading to the death of neurons. Additionally, the research introduces a method involving S100B, BAPTA, and calmodulin buffers to uphold optimal calcium levels within the neuronal cytosol. The applicability of this model with different buffer properties and parameters and memory impacts the calcium concentration with the neurological disorder.
钙离子作为各种细胞活动的调节因子,是第二信使。其时空控制对于包括神经可塑性、细胞凋亡和细胞死亡在内的各种脑功能至关重要。内质网(ER)在决定这些时空钙动力学方面发挥着重要作用。膜上的基质相互作用分子(STIM)-Orai通道产生额外的钙流,而其他膜通量则有助于胞质通量。由于它们的异常特性,我们使用Caputo分数微分算子在极坐标中模拟这些相互作用。使用混合积分变换方法生成解以控制分析方法。使用格林函数得到了米塔格-莱夫勒型函数的闭式解。这项工作强调了钙与神经元中各种缓冲水平之间的重要关系。跨不同参数的时间导数与空间的微分跃迁模拟表明钙浓度降低。异常低的缓冲水平显示出阿尔茨海默病对钙更高浓度的影响,导致神经元死亡。此外,该研究引入了一种涉及S100B、BAPTA和钙调蛋白缓冲剂的方法,以维持神经元胞质溶胶内的最佳钙水平。该模型在不同缓冲特性和参数下的适用性以及记忆会影响伴有神经疾病时的钙浓度。