Faculty of Dentistry, McGill University, Montreal, Quebec, Canada, H3A 1G1.
Shriners Hospital for Children - Canada, Montreal, Quebec, Canada, H4A 0A9.
J Cell Sci. 2018 Nov 21;131(22):jcs223354. doi: 10.1242/jcs.223354.
Body tissues are exposed to a complex mechanical environment, which is perceived by cells and converted to biochemical signals such as ATP release. We performed a meta-analysis of 278 systematically identified studies that investigated mechanically stimulated ATP release (MSAR) to quantify the amounts, kinetics and mechanisms of ATP release under normal and pathological conditions. Mechanically stimulated mammalian cells were shown to release 38.6 [95% confidence interval (CI): 18.2-81.8] amol ATP/cell on average with a characteristic time constant of 32 s (95% CI: 16-66). Analysis of ATP release mechanisms revealed the existence of conserved and tissue-specific release routes. We assessed ATP release in pathophysiological states, and found that ATP release was elevated in inflammation and injury, and attenuated in hereditary (such as cystic fibrosis) and metabolic (such as type II diabetes) conditions. Our study links cell-specific ATP release mechanisms to pathophysiological changes in ATP release and allows ATP release-targeting interventions to be mapped to site-specific effects. This work demonstrates that quantitative synthesis of basic research can generate non-trivial hypotheses and inform evidence-driven translational studies.
组织细胞暴露于复杂的机械环境中,这些环境被细胞感知并转化为生化信号,如 ATP 的释放。我们对 278 项经过系统鉴定的研究进行了荟萃分析,这些研究调查了机械刺激 ATP 释放(MSAR),以量化正常和病理条件下 ATP 释放的数量、动力学和机制。研究表明,机械刺激哺乳动物细胞平均释放 38.6 [95%置信区间(CI):18.2-81.8] amol ATP/细胞,特征时间常数为 32 s(95% CI:16-66)。对 ATP 释放机制的分析揭示了保守和组织特异性释放途径的存在。我们评估了病理生理状态下的 ATP 释放,发现炎症和损伤时 ATP 释放增加,遗传性(如囊性纤维化)和代谢性(如 II 型糖尿病)疾病时 ATP 释放减少。我们的研究将细胞特异性 ATP 释放机制与 ATP 释放的病理生理变化联系起来,并允许将针对 ATP 释放的干预措施映射到特定部位的效应。这项工作表明,基础研究的定量综合可以产生非平凡的假设,并为循证转化研究提供信息。