Developmental BioEngineering, MIRA Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente , 7522 NB Enschede, The Netherlands.
The Maastricht Multimodal Molecular Imaging Institute (M4I), Division of Imaging Mass Spectrometry, Maastricht University , 6229 ER Maastricht, The Netherlands.
Anal Chem. 2017 Sep 5;89(17):9438-9444. doi: 10.1021/acs.analchem.7b02265. Epub 2017 Aug 14.
Articular cartilage is exposed to a gradient of oxygen levels ranging from 5% at the surface to 1% in the deepest layers. While most cartilage research is performed in supraphysiological oxygen levels (19-21%), culturing chondrocytes under hypoxic oxygen levels (≤8%) promotes the chondrogenic phenotype. Exposure of cells to various oxygen levels alters their lipid metabolism, but detailed studies examining how hypoxia affects lipid metabolism in chondrocytes are lacking. To better understand the chondrocyte's behavior in response to oxygen, we cultured 3D pellets of human primary chondrocytes in normoxia (20% oxygen) and hypoxia (2.5% oxygen) and employed matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) in order to characterize the lipid profiles and their spatial distribution. In this work we show that chondrocytes cultured in hypoxia and normoxia can be differentiated by their lipid profiles. Among other species, phosphatidylglycerol species were increased in normoxic pellets, whereas phosphatidylinositol species were the most prominent lipids in hypoxic pellets. Moreover, spatial mapping revealed that phospahtidylglyycerol species were less prominent in the center of pellets where the oxygen level is lower. Additional analysis revealed a higher abundance of the mitochondrial-specific lipids, cardiolipins, in normoxic conditions. In conclusion MALDI-MSI described specific lipid profiles that could be used as sensors of oxygen level changes and may especially be relevant for retaining the chondrogenic phenotype, which has important implications for the treatment of bone and cartilage diseases.
关节软骨暴露在氧气浓度梯度中,表面的氧气浓度为 5%,而最深处的氧气浓度为 1%。虽然大多数软骨研究都是在超生理氧气水平(19-21%)下进行的,但在低氧氧气水平(≤8%)下培养软骨细胞会促进软骨细胞的表型。细胞暴露在不同的氧气水平会改变它们的脂质代谢,但缺乏详细研究来检查低氧如何影响软骨细胞的脂质代谢。为了更好地了解软骨细胞对氧气的反应行为,我们在常氧(20%氧气)和低氧(2.5%氧气)条件下培养了人原代软骨细胞的 3D 球状体,并采用基质辅助激光解吸电离质谱成像(MALDI-MSI)来描述脂质图谱及其空间分布。在这项工作中,我们表明在低氧和常氧条件下培养的软骨细胞可以通过它们的脂质图谱来区分。在其他物种中,磷脂酰甘油种类在常氧球状体中增加,而磷脂酰肌醇种类是低氧球状体中最主要的脂质。此外,空间映射显示,在氧气水平较低的球状体中心,磷脂酰甘油种类的丰度较低。进一步的分析显示,常氧条件下,线粒体特异性脂质心磷脂的丰度更高。总之,MALDI-MSI 描述了特定的脂质图谱,可以作为氧气水平变化的传感器,并且可能特别与保留软骨细胞表型有关,这对骨和软骨疾病的治疗具有重要意义。