Autophagy as a life support marker of isolated hepatocytes
Nataliya P. Bgatova , Raushan S. Dossymbekova , Julia S. Taskaeva , Svetlana M. Miroshnichenko , Roman A. Knyazev , Anastasia O. Solovieva , Kamalidin O. Sharipov , Zina B. Tungushbaeva
Morphology ›› 2021, Vol. 159 ›› Issue (1) : 5 -12.
Autophagy as a life support marker of isolated hepatocytes
AIM: The work aimed to reveal structural signs of autophagy in the cytoplasm of isolated hepatocytes in the dynamics of their cultivation.
MATERIALS AND METHODS: The cultivated hepatocyte culture cell cycle was studied by flow cytofluorometry. The cells were cultured for 1, 24, and 48 hours. Morphometric analysis was performed using of the computer program Image J. The diameters of the nuclei and cytoplasm of hepatocytes, the volumes of nuclei and cytoplasm, and the nuclear-cytoplasmic ratio were determined. The concentration of intracellular organelles and autophagy was evaluated with magnification by 30000 times.
RESULTS: The cell cycle arrest in the G0/G1 stage after 24 hours of hepatocyte cultivation and the preservation of their viability by hour 48 of the experiment without increase in the percentage of cells in the apoptosis stage were revealed. The decrease in the absolute count of cells was registered, as well as an increase in the nuclear-cytoplasmic ratio indicating a decrease in the proportion of hepatocyte cytoplasm in the course of cultivation. After 24 hours of cultivation, autophagosomes with fragments of cytoplasm, glycogen rosettes, and autolysosomes with partially degraded material were revealed in the cell cytoplasm. By hour 48 of the study, a significant decrease in the volume density of glycogen and mitochondria was noted, as well as an increase in basal autophagy in hepatocytes, with a prevalence of glycophagy and mitophagy.
CONCLUSIONS: Autophagy maintains cellular homeostasis of isolated hepatocytes under standard culture conditions, as evidenced by a decrease in the volume density of glycogen and mitochondria, and an increase in basal autophagy in the hepatocyte cytoplasm. The findings indicate the contribution of autophagy to the survival of the primary culture of hepatocytes and can be used as an indicator of the adequacy of culturing conditions.
isolated hepatocytes / cell cycle / basal autophagy
| [1] |
Ogoke O, Oluwole J, Parashurama N. Bioengineering considerations in liver regenerative medicine. J. Biol. Eng. 2017;11:6. doi: 10.1186/s13036-017-0081-4 |
| [2] |
Ogoke O., Oluwole J., Parashurama N. Bioengineering considerations in liver regenerative medicine // J. Biol. Eng. 2017. Vol. 11, № 6. doi: 10.1186/s13036-017-0081-4 |
| [3] |
Meyburg J, Hoffmann GF. Liver cell transplantation for the treatment of inborn errors of metabolism. J. Inherit. Metab. Dis. 2008; 31(2):164–172. doi: 10.1007/s10545-008-0829-6 |
| [4] |
Meyburg J., Hoffmann G.F. Liver cell transplantation for the treatment of inborn errors of metabolism // J. Inherit. Metab. Dis. 2008. Vol. 31, N 2. P. 164–172. doi: 10.1007/s10545-008-0829-6 |
| [5] |
Baccarani U, Adani GL, Sainz M, et al. Human hepatocyte transplantation for acute liver failure: state of the art and analysis of cell sources. Transplant. Proc. 2005;37(6):2702–04. doi: 10.1016/j.transproceed.2005.06.027 |
| [6] |
Baccarani U., Adani G.L., Sainz M., et al. Human hepatocyte transplantation for acute liver failure: state of the art and analysis of cell sources // Transplant. Proc. 2005. Vol. 37, N 6. P. 2702–04. doi: 10.1016/j.transproceed.2005.06.027 |
| [7] |
Akbari S, Sevinç GG, Ersoy N, et al. Robust, long-term culture of endoderm-derived hepatic organoids for disease modeling. Stem Cell Reports. 2019;13(4):627–641. doi: 10.1016/j.stemcr.2019.08.007 |
| [8] |
Akbari S., Sevinç G.G., Ersoy N., et al. Robust, long-term culture of endoderm-derived hepatic organoids for disease modeling // Stem Cell Reports. 2019. Vol. 13, N 4. P. 627–641. doi: 10.1016/j.stemcr.2019.08.007 |
| [9] |
Cao L, Wang J, Bo L, et al. Effects of hypoxia on the growth and development of the fetal ovine hepatocytes in primary culture. Biomed. Environ. Sci. 2019;32(8):592–601. doi: 10.3967/bes2019.077 |
| [10] |
Cao L., Wang J., Bo L., et al. Effects of hypoxia on the growth and development of the fetal ovine hepatocytes in primary culture // Biomed. Environ. Sci. 2019. Vol. 32, N 8. P. 592–601. doi: 10.3967/bes2019.077 |
| [11] |
Nicolas CT, Hickey RD, Chen HS, et al. Concise review: liver regenerative medicine: from hepatocyte transplantation to bioartificial livers and bioengineered grafts. Stem Cells. 2017;35(1):42–50. doi: 10.1002/stem.2500 |
| [12] |
Nicolas C.T., Hickey R.D., Chen H.S., et al. Concise review: liver regenerative medicine: from hepatocyte transplantation to bioartificial livers and bioengineered grafts // Stem Cells. 2017. Vol. 35, N 1. P. 42–50. doi: 10.1002/stem.2500 |
| [13] |
Olsavsky Goyak KM, Laurenzana EM, Omiecinski CJ. Hepatocyte differentiation. Methods Mol. Biol. 2010;640:115–38. doi: 10.1007/978-1-60761-688-7_6 |
| [14] |
Olsavsky Goyak K.M., Laurenzana E.M., Omiecinski C.J. Hepatocyte differentiation // Methods Mol. Biol. 2010. Vol. 640. P. 115–38. doi: 10.1007/978-1-60761-688-7_6 |
| [15] |
Sica V, Galluzzi L, Bravo-San Pedro JM, et al. Organelle-specific initiation of autophagy. Mol. Cell. 2015;59(4):522–39. doi: 10.1016/j.molcel.2015.07.021 |
| [16] |
Sica V., Galluzzi L., Bravo-San Pedro J.M., et al. Organelle-specific initiation of autophagy // Mol. Cell. 2015. Vol. 59, N 4. P. 522–39. doi: 10.1016/j.molcel.2015.07.021 |
| [17] |
Kroemer G, Jäättelä M. Lysosomes and autophagy in cell death control. Nat. Rev. Cancer. 2005;5(11):886–97. doi: 10.1038/nrc1738 |
| [18] |
Kroemer G., Jäättelä M. Lysosomes and autophagy in cell death control // Nat. Rev. Cancer. 2005. Vol. 5, N 11. P. 886–97. doi: 10.1038/nrc1738 |
| [19] |
Ha J, Guan KL, Kim J. AMPK and autophagy in glucose/glycogen metabolism. Mol. Aspects Med. 2015;46:46–62. doi: 10.1016/j.mam.2015.08.002 |
| [20] |
Ha J., Guan K.L., Kim J. AMPK and autophagy in glucose/glycogen metabolism // Mol. Aspects Med. 2015. Vol. 46. P. 46–62. doi: 10.1016/j.mam.2015.08.002 |
| [21] |
He L, Zhang J, Zhao J, et al. Autophagy: the last defense against cellular nutritional stress. Adv. Nutr. 2018;9(4):493–504. doi: 10.1093/advances/nmy011 |
| [22] |
He L., Zhang J., Zhao J., et al. Autophagy: the last defense against cellular nutritional stress. Adv. Nutr. 2018. Vol. 9, N 4. P. 493–504. doi: 10.1093/advances/nmy011 |
| [23] |
Krause P, Unthan-Fechner K, Probst I, Koenig S. Cultured hepatocytes adopt progenitor characteristics and display bipotent capacity to repopulate the liver. Cell Transplant. 2014;23(7):805–17. doi: 10.3727/096368913X664856 |
| [24] |
Krause P., Unthan-Fechner K., Probst I., Koenig S. Cultured hepatocytes adopt progenitor characteristics and display bipotent capacity to repopulate the liver // Cell Transplant. 2014. Vol. 23, N 7. P. 805–17. doi: 10.3727/096368913X664856 |
Bgatova N.P., Dossymbekova R.S., Taskaeva J.S., Miroshnichenko S.M., Knyazev R.A., Solovieva A.O., Sharipov K.O., Tungushbaeva Z.B.
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