Department of Pulmonary and Critical Care Medicine, Third Xiangya Hospital, Central South University, No.138 Tongzipo Road, Changsha, 410013, Hunan, China.
Hunan Key Laboratory of Organ Fibrosis, Changsha, China.
Sci Rep. 2024 Jun 22;14(1):14376. doi: 10.1038/s41598-024-64844-5.
Idiopathic pulmonary fibrosis (IPF) is believed to be associated with a notable disruption of cellular energy metabolism. By detecting the changes of energy metabolites in the serum of patients with pulmonary fibrosis, we aimed to investigate the diagnostic and prognostic value of energy metabolites in IPF, and further elucidated the mechanism of their involvement in pulmonary fibrosis. Through metabolomics research, it was discovered that the TCA cycle intermediates changed dramatically in IPF patients. In another validation cohort of 55 patients with IPF compared to 19 healthy controls, it was found that succinate, an intermediate product of TCA cycle, has diagnostic and prognostic value in IPF. The cut-off levels of serum succinate were 98.36 μM for distinguishing IPF from healthy controls (sensitivity, 83.64%; specificity, 63.16%; likelihood ratio, 2.27, respectively). Moreover, a high serum succinate level was independently associated with higher rates of disease progression (OR 13.087, 95%CI (2.819-60.761)) and mortality (HR 3.418, 95% CI (1.308-8.927)). In addition, accumulation of succinate and increased expression of the succinate receptor GPR91 were found in both IPF patients and BLM mouse models of pulmonary fibrosis. Reducing succinate accumulation in BLM mice alleviated pulmonary fibrosis and 21d mortality, while exogenous administration of succinate can aggravate pulmonary fibrosis in BLM mice. Furthermore, GPR91 deficiency protected against lung fibrosis caused by BLM. In vitro, succinate promoted the activation of lung fibroblasts by activating ERK pathway through GPR91. In summary, succinate is a promising biomarker for diagnosis and prognosis of IPF. The accumulation of succinate may promote fibroblast activation through GPR91 and pulmonary fibrosis.
特发性肺纤维化(IPF)被认为与细胞能量代谢的显著破坏有关。通过检测肺纤维化患者血清中的能量代谢物变化,我们旨在探讨能量代谢物在 IPF 中的诊断和预后价值,并进一步阐明其参与肺纤维化的机制。通过代谢组学研究,发现 IPF 患者 TCA 循环中间产物发生了显著变化。在另一项 55 例 IPF 患者与 19 例健康对照的验证队列中,发现 TCA 循环中间产物琥珀酸在 IPF 中有诊断和预后价值。区分 IPF 与健康对照的血清琥珀酸截断值为 98.36 μM(敏感性,83.64%;特异性,63.16%;似然比,2.27)。此外,高血清琥珀酸水平与疾病进展率较高(OR 13.087,95%CI(2.819-60.761))和死亡率(HR 3.418,95%CI(1.308-8.927))独立相关。此外,在 IPF 患者和博来霉素(BLM)诱导的肺纤维化小鼠模型中都发现了琥珀酸的积累和琥珀酸受体 GPR91 的表达增加。在 BLM 小鼠中减少琥珀酸的积累可以缓解肺纤维化和 21d 死亡率,而外源性给予琥珀酸可加重 BLM 小鼠的肺纤维化。此外,GPR91 缺乏可防止 BLM 引起的肺纤维化。体外,琥珀酸通过 GPR91 激活 ERK 通路促进肺成纤维细胞的激活。总之,琥珀酸是 IPF 诊断和预后的有前途的生物标志物。琥珀酸的积累可能通过 GPR91 促进成纤维细胞激活和肺纤维化。