Quiring Leonard, Caponi Luisa, Schwan Dhanusha, Rech Anja, Rauen Ursula
Klinische Forschergruppe 117, Universitätsklinikum Essen, Essen, Germany.
Institut für Physiologische Chemie, Universitätsklinikum Essen, Essen, Germany.
Front Transplant. 2022 Nov 3;1:1044551. doi: 10.3389/frtra.2022.1044551. eCollection 2022.
Mitochondrial integrity and function constitute a prerequisite for cellular function and repair processes. We have previously shown that mitochondria of different cell types exhibit pronounced fragmentation under hypothermic conditions. This fission, accompanied by a decline of cellular ATP content, showed reversibility at 37◦C. However, it is unclear whether other temperatures as currently discussed for reconditioning of organs allow this reconstitution of mitochondria. Therefore, we here study in a model of cultured porcine aortic endothelial cells how different rewarming temperatures affect mitochondrial re-fusion and function. After 48 h cold incubation of endothelial cells in Krebs-Henseleit buffer with glucose (5 mM) and deferoxamine (1 mM) at 4◦C pronounced mitochondrial fission was observed. Following 2 h rewarming in cell culture medium, marked fission was still present after rewarming at 10◦ or 15◦C. At 21◦C some re-fusion was visible, which became more marked at 25◦C. Networks of tubular mitochondria similar to control cells only re-appeared at 37◦C. ATP content decreased at 4◦C from 3.6 ± 0.4 to 1.6 ± 0.4 nmol/10 cells and decreased even further when rewarming cells to 10◦ and 15◦C. Values after rewarming at 21◦C were similar to the values before rewarming while ATP gradually increased at higher rewarming temperatures. Metabolic activity dropped to 5 ± 11% of control values during 4◦C incubation and recovered with increasing temperatures to 36 ± 10% at 25◦C and 78 ± 17% at 37◦C. Integrity of monolayers, largely disturbed at 4◦C (large gaps between endothelial cells; cell injury ≤ 1%), showed partial recovery from 15◦C upwards, complete recovery at 37◦C. Endothelial repair processes (scratch assay) at 25◦C were clearly inferior to those at 37◦C. These data suggest that reconditioning temperatures below 21◦C are not optimal with regard to reconstitution of mitochondrial integrity and function. For this goal, temperatures of at least 25◦C appear required, with 30◦C being superior and 37◦C yielding the best results.
线粒体的完整性和功能是细胞功能及修复过程的先决条件。我们之前已经表明,不同细胞类型的线粒体在低温条件下会出现明显的碎片化。这种裂变伴随着细胞ATP含量的下降,在37℃时显示出可逆性。然而,目前讨论的用于器官修复的其他温度是否能使线粒体重新恢复原状尚不清楚。因此,我们在培养的猪主动脉内皮细胞模型中研究不同的复温温度如何影响线粒体的重新融合和功能。在内皮细胞于含有葡萄糖(5 mM)和去铁胺(1 mM)的Krebs-Henseleit缓冲液中在4℃冷孵育48小时后,观察到明显的线粒体裂变。在细胞培养基中复温2小时后,在10℃或15℃复温后仍存在明显的裂变。在21℃时可见一些重新融合,在25℃时变得更加明显。类似于对照细胞的管状线粒体网络仅在37℃时重新出现。ATP含量在4℃时从3.6±0.4降至1.6±0.4 nmol/10个细胞,当细胞复温至10℃和15℃时甚至进一步下降。在21℃复温后的数值与复温前的数值相似,而在较高的复温温度下ATP逐渐增加。在4℃孵育期间代谢活性降至对照值的5±11%,并随着温度升高而恢复,在25℃时为36±10%,在37℃时为78±17%。单层的完整性在4℃时受到很大干扰(内皮细胞之间有大的间隙;细胞损伤≤1%),从15℃开始部分恢复,在37℃时完全恢复。在25℃时的内皮修复过程(划痕试验)明显不如在37℃时。这些数据表明,就线粒体完整性和功能的恢复而言,低于21℃的修复温度并非最佳。为了实现这一目标,似乎需要至少25℃的温度,30℃更佳,37℃产生的效果最好。