Effect of specific mutations in Cd300 complexes formation; Potential implication of Cd300f in multiple sclerosis

Águeda Martínez-Barriocanal, Andrea Arcas-García, Miriam Magallon-Lorenz, Aroa Ejarque-Ortíz, María Luciana Negro-Demontel, Emma Comas-Casellas, Simo Schwartz, Sunny Malhotra, Xavier Montalban, Hugo Peluffo, Margarita Martín, Manuel Comabella, Joan Sayós

Research output: Contribution to journalArticleResearchpeer-review

7 Citations (Scopus)


© 2017 The Author(s). Herein, we have used bioinformatics tools to predict five clusters defining ligand-binding sites on the extracellular domain of human CD300b receptor, presumably involved in the formation of both homodimers and heterodimers with other CD300 family members. Site-directed mutagenesis revealed residues glutamic acid 28 and glutamine 29 in cluster 5 to be necessary for the formation of CD300b complexes. Surprisingly, the disruption of cluster 2 and 4 reconstituted the binding capability lost by the mutation of residues glutamic acid 28 to alanine, glutamine 29 to alanine (E28A-Q29G). We identified a missense mutation arginine 33 to glutamine (R33Q) in CD300f by direct sequencing of exon 2 in peripheral blood samples from 50 patients with multiple sclerosis (MS). Levels of expression of CD300f were almost undetectable on monocytes from the patient bearing the R33Q mutation compared with healthy individuals. Whereas R33Q mutation had no effect in the formation of CD300f complexes, the inhibition of protein synthesis with cycloheximide indicated that CD300f R33Q is less stable than native CD300f. Finally, we report that the levels of expression of CD300f on the surface of classical and intermediate monocytes from MS patients are significantly lower when compared to the same cell populations in healthy individuals.
Original languageEnglish
Article number13544
Issue number1
Publication statusPublished - 1 Dec 2017


Dive into the research topics of 'Effect of specific mutations in Cd300 complexes formation; Potential implication of Cd300f in multiple sclerosis'. Together they form a unique fingerprint.

Cite this