UNCOUPLED RESPIRATION STABILITY OF ISOLATED PANCREATIC ACINI AS A NOVEL FUNCTIONAL TEST FOR CELL VITALITY

Anastasiia Zub, Bohdan V. Manko, Bohdan O. Manko, Volodymyr Manko, Andriy Babsky


DOI: http://dx.doi.org/10.30970/sbi.1703.735

Abstract


Background. Assessment of cell viability is crucial in cell studies. Testing plasma membrane integrity is a traditional approach of evaluating cell viability. Mitochondrial functional capacity closely correlates with plasma membrane integrity and overall cell health. This study aimed to investigate whether any aspect of mitochondrial adaptive capacity in isolated pancreatic acini is associated with the quality of said preparations, as determined by the dye exclusion method.
Materials and Methods. Experiments were carried out on male Wistar rats weig­hing 250–300 g. A suspension of isolated pancreatic acini was obtained using collagenase. The rate of oxygen consumption of rat isolated pancreatic acini was measured with Clark oxygen electrode. Basal respiration of isolated pancreatic acini was recorded for approximately 2 min. Afterwards, the mitochondrial adaptive capacity was examined using FCCP in concentrations from 0.5 to 2 μM. Uncoupled respiratory stability was calculated as a ratio of respiration rate at high and low FCCP concentrations. Plasma membrane integrity was assessed with trypan blue staining. A total of 74 preparations of isolated pancreatic acini were used in this study.
Results. In all experiments, 92–99 % of pancreatic acinar cells exhibited negative trypan blue staining, indicating intact plasma membranes. The basal and maximal uncoupled respiration rates were not affected by the fraction of trypan-negative cells. However, acini preparations with <less than 95 % plasma membrane integrity had significantly lower uncoupled respiration rates when exposed to a high concentration of FCCP (2 µM), indicating reduced stability of uncoupled respiration.
Conclusions. Results of the study suggest that the stability of uncoupled respiration can serve as a novel metabolic functional test to complement the existing methods for assessing cell vitality.


Keywords


pancreas, acinar cells, viability, uncoupled respiration

Full Text:

PDF

References


Armstrong, J. A., Cash, N. J., Ouyang, Y., Morton, J. C., Chvanov, M., Latawiec, D., Awais, M., Tepikin, A. V., Sutton, R., & Criddle, D. N. (2018). Oxidative stress alters mitochondrial bioenergetics and modifies pancreatic cell death independently of cyclophilin D, resulting in an apoptosis-to-necrosis shift. Journal of Biological Chemistry, 293(21), 8032-8047. doi:10.1074/jbc.ra118.003200
CrossrefPubMedPMCGoogle Scholar

Armstrong, J., Cash, N., Morton, J., Tepikin, A., Sutton, R., & Criddle, D. (2019). Mitochondrial targeting of antioxidants alters pancreatic acinar cell bioenergetics and determines cell fate. International Journal of Molecular Sciences, 20(7), 1700. doi:10.3390/ijms20071700
CrossrefPubMedPMCGoogle Scholar

Bock, F. J., & Tait, S. W. G. (2020). Mitochondria as multifaceted regulators of cell death. Nature Reviews Molecular Cell Biology, 21(2), 85-100. doi:10.1038/s41580-019-0173-8
CrossrefPubMedGoogle Scholar

Cassim, S., Martin, P.-Y., & Pascolo-Rebouillat, E. (2022). ADD10 protects renal cells from cold injuries by improving energy metabolism. Biochemical and Biophysical Research Communications, 634, 62-69. doi:10.1016/j.bbrc.2022.10.009
CrossrefPubMedGoogle Scholar

Horbay, R. O., Manko, B. O., Manko, V. V., Lootsik, M. D., & Stoika, R. S. (2012). Respiration characteristics of mitochondria in parental and giant transformed cells of the murine Nemeth-Kellner lymphoma. Cell Biology International, 36(1), 71-77. doi:10.1042/cbi20110017
CrossrefPubMedGoogle Scholar

Maléth, J., & Hegyi, P. (2016). Ca2+ toxicity and mitochondrial damage in acute pancreatitis: translational overview. Philosophical Transactions of the Royal Society B: Biological Sciences, 371(1700), 20150425. doi:10.1098/rstb.2015.0425
CrossrefPubMedPMCGoogle Scholar

Manko, B. O., Bilonoha, O. O., & Manko, V. V. (2019). Adaptive respiratory response of rat pancreatic acinar cells to mitochondrial membrane depolarization. The Ukrainian Biochemical Journal, 91(3). doi:10.15407/ubj91.03.034
CrossrefGoogle Scholar

Manko, B. O., Bilonoha, O. O., Voloshyn, D. M., Zub, A. M., Ivasechko, I. I., & Manko, V. V. (2021). Pyruvate and glutamine define the effects of cholecystokinin and ethanol on mitochondrial oxidation, necrosis, and morphology of rat pancreatic acini. Pancreas, 50(7). doi:10.1097/mpa.0000000000001864
CrossrefPubMedGoogle Scholar

Manko, B. O., Klevets, M. Yu., & Manko, V. V. (2013). An implication of novel methodology to study pancreatic acinar mitochondria under in situ conditions. Cell Biochemistry and Function, 31(2), 115-121. doi:10.1002/cbf.2864
CrossrefPubMedGoogle Scholar

Manko, B. O., & Manko, V. V. (2013). Influence of Ca2+ on kinetic parameters of pancreatic acinar mitochondria in situ respiration. The Ukrainian Biochemical Journal, 85(4), 48-60. doi:10.15407/ubj85.04.048 (In Ukrainian)
CrossrefPubMedGoogle Scholar

Pesta, D., & Gnaiger, E. (2012). High-resolution respirometry: OXPHOS protocols for human cells and permeabilized fibers from small biopsies of human muscle. In: C. Palmeira & A. Moreno (Eds.), Mitochondrial bioenergetics. Methods in molecular biology (Vol 810, pp. 25-58). Humana Press. doi:10.1007/978-1-61779-382-0_3
CrossrefPubMedGoogle Scholar

Pfleger, J., He, M., & Abdellatif, M. (2015). Mitochondrial complex II is a source of the reserve respiratory capacity that is regulated by metabolic sensors and promotes cell survival. Cell Death & Disease, 6(7), e1835-e1835. doi:10.1038/cddis.2015.202
CrossrefPubMedPMCGoogle Scholar

Rose, S., Carvalho, E., Diaz, E. C., Cotter, M., Bennuri, S. C., Azhar, G., Frye, R. E., Adams, S. H., & Børsheim, E. (2019). A comparative study of mitochondrial respiration in circulating blood cells and skeletal muscle fibers in women. American Journal of Physiology-Endocrinology and Metabolism, 317(3), E503-E512. doi:10.1152/ajpendo.00084.2019
CrossrefPubMedGoogle Scholar

Shrestha, N., Cuffe, J. S. M., Holland, O. J., & Perkins, A. V. (2019). Linoleic acid increases prostaglandin E2 release and reduces mitochondrial respiration and cell viability in human trophoblast-like cells. Cellular Physiology and Biochemistry, 52(1), 94-108. doi:10.33594/000000007
CrossrefPubMedGoogle Scholar

Stepanenko, A. A., & Dmitrenko, V. V. (2015). Pitfalls of the MTT assay: direct and off-target effects of inhibitors can result in over/underestimation of cell viability. Gene, 574(2), 193-203. doi:10.1016/j.gene.2015.08.009
CrossrefPubMed ● Google Scholar

Yan, X., Shi, Z. F., Xu, L. X., Li, J. X., Wu, M., Wang, X. X., Jia, M., Dong, L. P., Yang, S. H., & Yuan, F. (2017). Glutamate impairs mitochondria aerobic respiration capacity and enhances glycolysis in cultured rat astrocytes. Biomedical and Environmental Sciences, 30(1), 44-51. doi:10.3967/bes2017.005
CrossrefPubMedGoogle Scholar


Refbacks

  • There are currently no refbacks.


Copyright (c) 2023 Anastasiia Zub, Bohdan V. Manko, Bohdan O. Manko, Volodymyr Manko, Andriy Babsky

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.