TNFα-mediated subcellular heterogeneity of succinate dehydrogenase activity in human airway smooth muscle cells.

IF 3.6 2区 医学 Q1 PHYSIOLOGY
Sanjana Mahadev Bhat, Claire Catherine Creighton, Gary C Sieck
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引用次数: 0

Abstract

Tumor necrosis factor-α (TNFα) is a pro-inflammatory cytokine, which mediates acute inflammatory effects in response to allergens, pollutants, and respiratory infections. Previously, we reported that TNFα increased maximum O2 consumption rate (OCR) and mitochondrial volume density (MVD) in human airway smooth muscle (hASM) cells. However, TNFα decreased maximum OCR when normalized to mitochondrial volume. In addition, TNFα altered mitochondrial distribution and motility within hASM cells. Although high-resolution respirometry is valuable for assessing mitochondrial function, it overlooks mitochondrial structural and functional heterogeneity within cells. Therefore, a direct measurement of cellular mitochondrial function provides valuable information. Previously, we developed a confocal-based quantitative histochemical technique to determine the maximum velocity of the succinate dehydrogenase (SDH) reaction (SDHmax) in single cells and observed that cellular SDHmax corresponds with MVD. Therefore, we hypothesized that TNFα decreases SDHmax per mitochondrion in hASM cells. The hASM cells were treated with TNFα (20 ng/mL, 6 h, and 24 h) or untreated (time-matched control). Using three-dimensional (3-D) confocal imaging of labeled mitochondria and a concentric shell method for analysis, we quantified MVD, mitochondrial complexity index (MCI) and SDHmax relative to the nuclear membrane. Within each shell, SDHmax and MVD peaked in the perinuclear compartments and decreased toward the distal compartments of the cell. When normalized to mitochondrial volume, SDHmax decreased in the perinuclear compartments compared with distal compartments. TNFα caused a significant shift in mitochondrial morphometry and function compared to control. In conclusion, mitochondria within individual cells exhibit distinct morphological and functional heterogeneity, which is disrupted during acute inflammation.NEW & NOTEWORTHY Mitochondria show context-specific heterogeneity in their morphometry. Previously, we reported that acute TNFα exposure increased O2 consumption rate (OCR) and mitochondrial volume density, but decreased OCR per mitochondrion. TNFα also altered mitochondrial distribution and motility. To assess TNFα-mediated subcellular mitochondrial structural and functional heterogeneity, we used a confocal-based quantitative histochemical technique to determine the maximum velocity of succinate dehydrogenase reaction. Our findings highlight that mitochondria within cells exhibit functional heterogeneity, which is disrupted during inflammation.

tnf α介导的人气道平滑肌细胞琥珀酸脱氢酶活性的亚细胞异质性。
肿瘤坏死因子-α (tnf -α)是一种促炎细胞因子,在对过敏原、污染物和呼吸道感染的反应中介导急性炎症效应。先前,我们报道了TNFα增加人气道平滑肌(hASM)细胞的最大氧气消耗率(OCR)和线粒体体积密度(MVD)。然而,当归一化到线粒体体积时,TNFα降低了最大的OCR。此外,TNFα改变了hASM细胞内的线粒体分布和运动。尽管高分辨率呼吸测量法对评估线粒体功能很有价值,但它忽略了细胞内线粒体结构和功能异质性。因此,直接测量细胞线粒体功能提供了有价值的信息。在此之前,我们开发了一种基于共聚焦的定量组织化学技术来确定单细胞中琥珀酸脱氢酶(SDH)反应(SDHmax)的最大速度,并观察到细胞SDHmax与MVD相对应。因此,我们假设TNFα降低了hASM细胞中每个线粒体的SDHmax。将hASM细胞用TNFα (20 ng/mL, 6 h和24 h)处理或不处理(时间匹配对照)。利用标记线粒体的三维共聚焦成像和同心壳法进行分析,我们量化了相对于核膜的MVD、线粒体复杂性指数(MCI)和SDHmax。在每个壳内,SDHmax和MVD在核周室中达到峰值,并向细胞的远端室降低。当将线粒体体积归一化时,与远端区室相比,核周围区室的SDHmax降低。与对照组相比,TNFα引起线粒体形态和功能的显著变化。总之,单个细胞内的线粒体表现出明显的形态和功能异质性,在急性炎症期间被破坏。新的和值得注意的线粒体在形态计量上显示出上下文特异性的异质性。先前,我们报道急性TNFα暴露增加了O2消耗率(OCR)和线粒体体积密度,但降低了每个线粒体的OCR。TNFα也改变了线粒体分布和运动。为了评估tnf α介导的亚细胞线粒体结构和功能异质性,我们使用基于共聚焦的定量组织化学技术来确定琥珀酸脱氢酶反应的最大速度。我们的研究结果强调,细胞内的线粒体表现出功能异质性,在炎症期间被破坏。
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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