Journal article

Hypercapnia Impairs Na,K-ATPase Function by Inducing Endoplasmic Reticulum Retention of the β-Subunit of the Enzyme in Alveolar Epithelial Cells


Authors listKryvenko, Vitalii; Wessendorf, Miriam; Morty, Rory E.; Herold, Susanne; Seeger, Werner; Vagin, Olga; Dada, Laura A.; Sznajder, Jacob, I; Vadasz, Istvan

Publication year2020

JournalInternational Journal of Molecular Sciences

Volume number21

Issue number4

eISSN1422-0067

Open access statusGold

DOI Linkhttps://doi.org/10.3390/ijms21041467

PublisherMDPI


Abstract
Alveolar edema, impaired alveolar fluid clearance, and elevated CO2 levels (hypercapnia) are hallmarks of the acute respiratory distress syndrome (ARDS). This study investigated how hypercapnia affects maturation of the Na,K-ATPase (NKA), a key membrane transporter, and a cell adhesion molecule involved in the resolution of alveolar edema in the endoplasmic reticulum (ER). Exposure of human alveolar epithelial cells to elevated CO2 concentrations caused a significant retention of NKA-beta in the ER and, thus, decreased levels of the transporter in the Golgi apparatus. These effects were associated with a marked reduction of the plasma membrane (PM) abundance of the NKA-alpha/beta complex as well as a decreased total and ouabain-sensitive ATPase activity. Furthermore, our study revealed that the ER-retained NKA-beta subunits were only partially assembled with NKA alpha-subunits, which suggests that hypercapnia modifies the ER folding environment. Moreover, we observed that elevated CO2 levels decreased intracellular ATP production and increased ER protein and, particularly, NKA-beta oxidation. Treatment with alpha-ketoglutaric acid (alpha-KG), which is a metabolite that has been shown to increase ATP levels and rescue mitochondrial function in hypercapnia-exposed cells, attenuated the deleterious effects of elevated CO2 concentrations and restored NKA PM abundance and function. Taken together, our findings provide new insights into the regulation of NKA in alveolar epithelial cells by elevated CO2 levels, which may lead to the development of new therapeutic approaches for patients with ARDS and hypercapnia.



Citation Styles

Harvard Citation styleKryvenko, V., Wessendorf, M., Morty, R., Herold, S., Seeger, W., Vagin, O., et al. (2020) Hypercapnia Impairs Na,K-ATPase Function by Inducing Endoplasmic Reticulum Retention of the β-Subunit of the Enzyme in Alveolar Epithelial Cells, International Journal of Molecular Sciences, 21(4), Article 1467. https://doi.org/10.3390/ijms21041467

APA Citation styleKryvenko, V., Wessendorf, M., Morty, R., Herold, S., Seeger, W., Vagin, O., Dada, L., Sznajder, J., & Vadasz, I. (2020). Hypercapnia Impairs Na,K-ATPase Function by Inducing Endoplasmic Reticulum Retention of the β-Subunit of the Enzyme in Alveolar Epithelial Cells. International Journal of Molecular Sciences. 21(4), Article 1467. https://doi.org/10.3390/ijms21041467



Keywords


ALPHA-KETOGLUTARATEalveolar epitheliumEdemaEndoplasmic reticulumHYPERCAPNIANa,K-ATPasePROTEIN CARBONYLATIONprotein oxidationQUALITY-CONTROLsodium transport

Last updated on 2025-10-06 at 11:10