Fovez Quentin, Laine William, Goursaud Laure, Berthon Celine, Germain Nicolas, Degand Claire, Sarry Jean-Emmanuel, Quesnel Bruno, Marchetti Philippe, Kluza Jerome
Institut pour la Recherche sur le Cancer de Lille, Univ. Lille, CNRS, Inserm, CHU Lille, UMR9020-UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, F-59000 Lille, France.
Hematology Department, CHU Lille, F-59000 Lille, France.
Cancers (Basel). 2021 Dec 17;13(24):6353. doi: 10.3390/cancers13246353.
Resistant acute myeloid leukemia (AML) exhibits mitochondrial energy metabolism changes compared to newly diagnosed AML. This phenotype is often observed by evaluating the mitochondrial oxygen consumption of blasts, but most of the oximetry protocols were established from leukemia cell lines without validation on primary leukemia cells. Moreover, the cultures and storage conditions of blasts freshly extracted from patient blood or bone marrow cause stress, which must be evaluated before determining oxidative phosphorylation (OXPHOS). Herein, we evaluated different conditions to measure the oxygen consumption of blasts using extracellular flow analyzers. We first determined the minimum number of blasts required to measure OXPHOS. Next, we compared the OXPHOS of blasts cultured for 3 h and 18 h after collection and found that to maintain metabolic organization for 18 h, cytokine supplementation is necessary. Cytokines are also needed when measuring OXPHOS in cryopreserved, thawed and recultured blasts. Next, the concentrations of respiratory chain inhibitors and uncoupler FCCP were established. We found that the FCCP concentration required to reach the maximal respiration of blasts varied depending on the patient sample analyzed. These protocols provided can be used in future clinical studies to evaluate OXPHOS as a biomarker and assess the efficacy of treatments targeting mitochondria.
与新诊断的急性髓系白血病(AML)相比,耐药性急性髓系白血病表现出线粒体能量代谢变化。这种表型通常通过评估原始细胞的线粒体氧消耗来观察,但大多数血氧测定方案是基于白血病细胞系建立的,未在原发性白血病细胞上进行验证。此外,从患者血液或骨髓中新鲜提取的原始细胞的培养和储存条件会造成应激,这在确定氧化磷酸化(OXPHOS)之前必须进行评估。在此,我们使用细胞外流量分析仪评估了测量原始细胞氧消耗的不同条件。我们首先确定了测量OXPHOS所需的原始细胞的最小数量。接下来,我们比较了采集后培养3小时和18小时的原始细胞的OXPHOS,发现为了维持18小时的代谢组织,补充细胞因子是必要的。在对冷冻保存、解冻和重新培养的原始细胞测量OXPHOS时也需要细胞因子。接下来,确定了呼吸链抑制剂和解偶联剂FCCP的浓度。我们发现,达到原始细胞最大呼吸所需的FCCP浓度因所分析的患者样本而异。所提供的这些方案可用于未来的临床研究,以评估OXPHOS作为生物标志物,并评估针对线粒体的治疗效果。