The β2-Subunit (AMOG) of Human Na+, K+-ATPase Is a Homophilic Adhesion Molecule
Authors:
- María Luisa RoldánMRMaría Luisa Roldán
- Gema Lizbeth Ramírez-SalinasGRGema Lizbeth Ramírez-Salinas
- Marlet Martinez-ArchundiaMMMarlet Martinez-Archundia
- Francisco Cuellar-PerezFCFrancisco Cuellar-Perez
- Claudia Andrea Vilchis-NestorCVClaudia Andrea Vilchis-Nestor
- Juan Carlos Cancino-DiazJCJuan Carlos Cancino-Diaz
- Liora ShoshaniLSLiora Shoshani
Open Access
- 14 July 2022
- journal article
- research article
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 23 (14) , 7753
Abstract
The β2 subunit of Na+, K+-ATPase was originally identified as the adhesion molecule on glia (AMOG) that mediates the adhesion of astrocytes to neurons in the central nervous system and that is implicated in the regulation of neurite outgrowth and neuronal migration. While β1 isoform have been shown to trans-interact in a species-specific mode with the β1 subunit on the epithelial neighboring cell, the β2 subunit has been shown to act as a recognition molecule on the glia. Nevertheless, none of the works have identified the binding partner of β2 or described its adhesion mechanism. Until now, the interactions pronounced for β2/AMOG are heterophilic cis-interactions. In the present report we designed experiments that would clarify whether β2 is a cell–cell homophilic adhesion molecule. For this purpose, we performed protein docking analysis, cell–cell aggregation, and protein–protein interaction assays. We observed that the glycosylated extracellular domain of β2/AMOG can make an energetically stable trans-interacting dimer. We show that CHO (Chinese Hamster Ovary) fibroblasts transfected with the human β2 subunit become more adhesive and make large aggregates. The treatment with Tunicamycin in vivo reduced cell aggregation, suggesting the participation of N-glycans in that process. Protein–protein interaction assay in vivo with MDCK (Madin-Darby canine kidney) or CHO cells expressing a recombinant β2 subunit show that the β2 subunits on the cell surface of the transfected cell lines interact with each other. Overall, our results suggest that the human β2 subunit can form trans-dimers between neighboring cells when expressed in non-astrocytic cells, such as fibroblasts (CHO) and epithelial cells (MDCK).Keywords
Funding Information
- “Secretaria e Investigación de Posgrado (SIP)” of the National Polytechnic Institute (IPN) (2143 (20220662), 48798)
- Secretaría de Ciencia, Humanidades, Tecnología e Innovación (2143 (20220662), 48798)
This publication has 47 references indexed in Scilit:
- Identification of the amino-acid region involved in the intercellular interaction between the Na,K-ATPase β1 subunitsJournal of Cell Science, 2012
- The Polarized Distribution of Na+,K+-ATPase: Role of the Interaction between β SubunitsMolecular Biology of the Cell, 2010
- Inverse Correlation between the Extent of N-Glycan Branching and Intercellular Adhesion in EpitheliaJournal of Biological Chemistry, 2008
- Prion Protein Regulates Glutamate-Dependent Lactate Transport of AstrocytesJournal of Neuroscience, 2007
- Deglycosylation of Na+/K+-ATPase causes the basolateral protein to undergo apical targeting in polarized hepatic cellsJournal of Cell Science, 2006
- UCSF Chimera—A visualization system for exploratory research and analysisJournal of Computational Chemistry, 2004
- Intermediate filament–membrane attachments function synergistically with actin-dependent contacts to regulate intercellular adhesive strengthJournal of Cell Biology, 2002
- All three potential N-glycosylation sites of the dog kidney (Na+ + K+)-ATPase β-subunit contain oligosaccharideBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1988
- THE (Na++K+)‐ATPase: COUPLING OF THE REACTION WITH ATP TO THE REACTION WITH Na+ AND K+Annals of the New York Academy of Sciences, 1982
- Preparation of highly active (Na+ + K+)-ATPase from the outer medulla of rabbit kidneyBiochemical and Biophysical Research Communications, 1969