Fulwah Yahya Saleh Alqahtani
Deciphering the complex three-way interaction between the non-integrin laminin receptor, galectin-3 and Neisseria meningitidis
Alqahtani, Fulwah Yahya Saleh; Mahdavi, Jafar; Wheldon, Lee M.; Vassey, Matthew; Pirinccioglu, Necmettin; Royer, Pierre-Joseph; Qarani, Suzan M.; Morroll, Shaun; Stoof, Jeroen; Holliday, Nicholas D.; Teo, Siew Y.; Oldfield, Neil J.; Wooldridge, Karl G.; Ala'Aldeen, Dlawer A.A.
Authors
Jafar Mahdavi
Lee M. Wheldon
Matthew Vassey
Necmettin Pirinccioglu
Pierre-Joseph Royer
Suzan M. Qarani
Shaun Morroll
Jeroen Stoof
Nicholas D. Holliday
Siew Y. Teo
Neil J. Oldfield
Karl G. Wooldridge
Dlawer A.A. Ala'Aldeen
Abstract
The non-integrin laminin receptor (LAMR1/RPSA) and galectin-3 (Gal-3) are multi-functional host molecules with roles in diverse pathological processes, particularly of infectious or oncogenic origins. Using bimolecular fluorescence complementation and confocal imaging, we demonstrate that the two proteins homo- and heterodimerize, and that each isotype forms a distinct cell surface population. We present evidence that the 37 kDa form of LAMR1 (37LRP) is the precursor of the previously described 67 kDa laminin receptor (67LR), whereas the heterodimer represents an entity that is distinct from this molecule. Site-directed mutagenesis confirmed that the single cysteine (C173) of Gal-3 or lysine (K166) of LAMR1 are critical for heterodimerization. Recombinant Gal-3, expressed in normally Gal-3-deficient N2a cells, dimerized with endogenous LAMR1 and led to a significantly increased number of internalized bacteria (Neisseria meningitidis), confirming the role of Gal-3 in bacterial invasion. Contact-dependent cross-linking determined that, in common with LAMR1, Gal-3 binds the meningococcal secretin PilQ, in addition to the major pilin PilE. This study adds significant new mechanistic insights into the bacterial–host cell interaction by clarifying the nature, role and bacterial ligands of LAMR1 and Gal-3 isotypes during colonization.
Citation
Alqahtani, F. Y. S., Mahdavi, J., Wheldon, L. M., Vassey, M., Pirinccioglu, N., Royer, P.-J., …Ala'Aldeen, D. A. (2014). Deciphering the complex three-way interaction between the non-integrin laminin receptor, galectin-3 and Neisseria meningitidis. Open Biology, 4(10), Article 140053. https://doi.org/10.1098/rsob.140053
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 2, 2014 |
Publication Date | Oct 1, 2014 |
Deposit Date | Jul 12, 2016 |
Publicly Available Date | Jul 12, 2016 |
Journal | Open Biology |
Electronic ISSN | 2046-2441 |
Publisher | The Royal Society |
Peer Reviewed | Peer Reviewed |
Volume | 4 |
Issue | 10 |
Article Number | 140053 |
DOI | https://doi.org/10.1098/rsob.140053 |
Keywords | LAMR1, RPSA, galectin-3, 37LRP, 67LR, Neisseria meningitidis |
Public URL | https://nottingham-repository.worktribe.com/output/734562 |
Publisher URL | http://rsob.royalsocietypublishing.org/content/4/10/140053 |
Contract Date | Jul 12, 2016 |
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Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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