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Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality. / Katkova, Liubov E.; Baturina, Galina S.; Bondar, Alexander A. et al.

In: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, Vol. 52, No. 4, 01.01.2019, p. 869-878.

Research output: Contribution to journalArticlepeer-review

Harvard

Katkova, LE, Baturina, GS, Bondar, AA, Jagirdar, RM, Hatzoglou, C, Gourgoulianis, KI, Solenov, EI & Zarogiannis, SG 2019, 'Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality', Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, vol. 52, no. 4, pp. 869-878. https://doi.org/10.33594/000000060

APA

Katkova, L. E., Baturina, G. S., Bondar, A. A., Jagirdar, R. M., Hatzoglou, C., Gourgoulianis, K. I., Solenov, E. I., & Zarogiannis, S. G. (2019). Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 52(4), 869-878. https://doi.org/10.33594/000000060

Vancouver

Katkova LE, Baturina GS, Bondar AA, Jagirdar RM, Hatzoglou C, Gourgoulianis KI et al. Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology. 2019 Jan 1;52(4):869-878. doi: 10.33594/000000060

Author

Katkova, Liubov E. ; Baturina, Galina S. ; Bondar, Alexander A. et al. / Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality. In: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology. 2019 ; Vol. 52, No. 4. pp. 869-878.

BibTeX

@article{8c717881280b4de9b78896f852c90e7c,
title = "Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality",
abstract = "Background/Aims: Cell volume regulation is a critical mechanism for cell homeostasis and depends on the osmotic water permeability (Pf) of the cell plasma membrane. The Pf of human mesothelial cells is unknown although they contribute to serosal fluid turnover. Methods: In this study we measured the osmotic water permeability of benign human mesothelial cells (MeT-5A) and of epithelioid (M14K) and sarcomatoid (ZL34) malignant pleural mesothelioma (MPM) cells in response to acute hyperosmotic stress. We also assessed the changes in their Pf after preconditioning with 4% glucose for 24 hours. In both cases we also assessed the role of AQP1 inhibition (0.1 mM HgCl2) on the Pf. Finally, we assessed corresponding changes in the AQP1 plasma membrane availability by immunofluorescence. Results: We report that MeT-5A cells have a significantly higher Pf as compared to M14K and ZL34 MPM cells [4.85E-03±2.37E-03 cm/sec (n=17) versus 2.74E-03±0.74E-03 cm/sec (n=11) and 2.86E-03±0.11E-03 cm/sec (n=11)]. AQP1 inhibition significantly decreased the Pf in all cells lines (p<0.001 in all cases). High glucose preconditioning for 24 hours significantly increased MeT-5A Pf (p<0.001), did not influence M14K Pf (p=0.19) and significantly reduced ZL34 Pf (p=0.02). Comparing cell lines after high glucose preconditioning, MeT-5A Pf was significantly higher than that of M14K and ZL34 MPM cells and the AQP1 inhibition effect was significant in MeT-5A and M14K cells. These results were corroborated by AQP1 immunofluorescence. Conclusion: We provide evidence for a differential regulation of Pf in benign and MPM cells that require further mechanistic investigation.",
keywords = "AQP1, Hyperosmotic stress, Malignant pleural mesothelioma, Osmotic water permeability, Pleural mesothelial cells, Aquaporin 1/metabolism, Osmotic Pressure, Humans, Mesothelioma/metabolism, Permeability, Pleural Neoplasms/metabolism, Cell Line, Tumor, Pleura/metabolism, Neoplasm Proteins/metabolism",
author = "Katkova, {Liubov E.} and Baturina, {Galina S.} and Bondar, {Alexander A.} and Jagirdar, {Rajesh M.} and Chrissi Hatzoglou and Gourgoulianis, {Konstantinos I.} and Solenov, {Evgeniy I.} and Zarogiannis, {Sotirios G.}",
note = "Publisher Copyright: {\textcopyright} 2019 Published The Author(s).",
year = "2019",
month = jan,
day = "1",
doi = "10.33594/000000060",
language = "English",
volume = "52",
pages = "869--878",
journal = "Cellular Physiology and Biochemistry",
issn = "1015-8987",
publisher = "S. Karger AG",
number = "4",

}

RIS

TY - JOUR

T1 - Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality

AU - Katkova, Liubov E.

AU - Baturina, Galina S.

AU - Bondar, Alexander A.

AU - Jagirdar, Rajesh M.

AU - Hatzoglou, Chrissi

AU - Gourgoulianis, Konstantinos I.

AU - Solenov, Evgeniy I.

AU - Zarogiannis, Sotirios G.

N1 - Publisher Copyright: © 2019 Published The Author(s).

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Background/Aims: Cell volume regulation is a critical mechanism for cell homeostasis and depends on the osmotic water permeability (Pf) of the cell plasma membrane. The Pf of human mesothelial cells is unknown although they contribute to serosal fluid turnover. Methods: In this study we measured the osmotic water permeability of benign human mesothelial cells (MeT-5A) and of epithelioid (M14K) and sarcomatoid (ZL34) malignant pleural mesothelioma (MPM) cells in response to acute hyperosmotic stress. We also assessed the changes in their Pf after preconditioning with 4% glucose for 24 hours. In both cases we also assessed the role of AQP1 inhibition (0.1 mM HgCl2) on the Pf. Finally, we assessed corresponding changes in the AQP1 plasma membrane availability by immunofluorescence. Results: We report that MeT-5A cells have a significantly higher Pf as compared to M14K and ZL34 MPM cells [4.85E-03±2.37E-03 cm/sec (n=17) versus 2.74E-03±0.74E-03 cm/sec (n=11) and 2.86E-03±0.11E-03 cm/sec (n=11)]. AQP1 inhibition significantly decreased the Pf in all cells lines (p<0.001 in all cases). High glucose preconditioning for 24 hours significantly increased MeT-5A Pf (p<0.001), did not influence M14K Pf (p=0.19) and significantly reduced ZL34 Pf (p=0.02). Comparing cell lines after high glucose preconditioning, MeT-5A Pf was significantly higher than that of M14K and ZL34 MPM cells and the AQP1 inhibition effect was significant in MeT-5A and M14K cells. These results were corroborated by AQP1 immunofluorescence. Conclusion: We provide evidence for a differential regulation of Pf in benign and MPM cells that require further mechanistic investigation.

AB - Background/Aims: Cell volume regulation is a critical mechanism for cell homeostasis and depends on the osmotic water permeability (Pf) of the cell plasma membrane. The Pf of human mesothelial cells is unknown although they contribute to serosal fluid turnover. Methods: In this study we measured the osmotic water permeability of benign human mesothelial cells (MeT-5A) and of epithelioid (M14K) and sarcomatoid (ZL34) malignant pleural mesothelioma (MPM) cells in response to acute hyperosmotic stress. We also assessed the changes in their Pf after preconditioning with 4% glucose for 24 hours. In both cases we also assessed the role of AQP1 inhibition (0.1 mM HgCl2) on the Pf. Finally, we assessed corresponding changes in the AQP1 plasma membrane availability by immunofluorescence. Results: We report that MeT-5A cells have a significantly higher Pf as compared to M14K and ZL34 MPM cells [4.85E-03±2.37E-03 cm/sec (n=17) versus 2.74E-03±0.74E-03 cm/sec (n=11) and 2.86E-03±0.11E-03 cm/sec (n=11)]. AQP1 inhibition significantly decreased the Pf in all cells lines (p<0.001 in all cases). High glucose preconditioning for 24 hours significantly increased MeT-5A Pf (p<0.001), did not influence M14K Pf (p=0.19) and significantly reduced ZL34 Pf (p=0.02). Comparing cell lines after high glucose preconditioning, MeT-5A Pf was significantly higher than that of M14K and ZL34 MPM cells and the AQP1 inhibition effect was significant in MeT-5A and M14K cells. These results were corroborated by AQP1 immunofluorescence. Conclusion: We provide evidence for a differential regulation of Pf in benign and MPM cells that require further mechanistic investigation.

KW - AQP1

KW - Hyperosmotic stress

KW - Malignant pleural mesothelioma

KW - Osmotic water permeability

KW - Pleural mesothelial cells

KW - Aquaporin 1/metabolism

KW - Osmotic Pressure

KW - Humans

KW - Mesothelioma/metabolism

KW - Permeability

KW - Pleural Neoplasms/metabolism

KW - Cell Line, Tumor

KW - Pleura/metabolism

KW - Neoplasm Proteins/metabolism

UR - http://www.scopus.com/inward/record.url?scp=85064503933&partnerID=8YFLogxK

U2 - 10.33594/000000060

DO - 10.33594/000000060

M3 - Article

C2 - 30958661

AN - SCOPUS:85064503933

VL - 52

SP - 869

EP - 878

JO - Cellular Physiology and Biochemistry

JF - Cellular Physiology and Biochemistry

SN - 1015-8987

IS - 4

ER -

ID: 19628622