TY - JOUR
T1 - Identification of a novel conserved signaling motif in CD200 receptor required for its inhibitory function
AU - Timmerman, Laura M.
AU - De Graaf, J. Fréderique
AU - Satravelas, Nikolaos
AU - Kesmir, Çan
AU - Meyaard, Linde
AU - Van Der Vlist, Michiel
N1 - Funding Information:
JFG, NS and CK received no specific funding for this work. LM, LMT and MV received funding from Oncode Institute (https://www. oncode.nl/). LM received funding from the Netherlands Organization for Scientific Research (NWO; https://www.nwo.nl/; ALW Grant 821.02.025 and NWO Vici 918.15.608). MV received funding from the Netherlands Organization for Scientific Research (NWO; https:// www.nwo.nl/; ALW Grant 863.14.016). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
Copyright © 2021 Timmerman et al.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/3/29
Y1 - 2021/3/29
N2 - The inhibitory signaling of CD200 receptor 1 (CD200R) has been attributed to its NPxY signaling motif. However, NPxY-motifs are present in multiple protein families and are mostly known to mediate protein trafficking between subcellular locations rather than signaling. Therefore, we investigated whether additional motifs specify the inhibitory function of CD200R. We performed phylogenetic analysis of the intracellular domain of CD200R in mammals, birds, bony fish, amphibians and reptiles. Indeed, the tyrosine of the NPxY-motif is fully conserved across species, in line with its central role in CD200R signaling. In contrast, P295 of the NPxY-motif is not conserved. Instead, a conserved stretch of negatively charged amino acids, EEDE279, and two conserved residues P285 and K292 in the flanking region prior to the NPxY-motif are required for CD200R mediated inhibition of p-Erk, pAkt308, p-Akt473, p-rpS6 and LPS-induced IL-8 secretion. Altogether, we show that instead of the more common NPxY-motif, CD200R signaling can be assigned to a unique signaling motif in mammals defined by: EEDExxPYxxYxxKxNxxY.
AB - The inhibitory signaling of CD200 receptor 1 (CD200R) has been attributed to its NPxY signaling motif. However, NPxY-motifs are present in multiple protein families and are mostly known to mediate protein trafficking between subcellular locations rather than signaling. Therefore, we investigated whether additional motifs specify the inhibitory function of CD200R. We performed phylogenetic analysis of the intracellular domain of CD200R in mammals, birds, bony fish, amphibians and reptiles. Indeed, the tyrosine of the NPxY-motif is fully conserved across species, in line with its central role in CD200R signaling. In contrast, P295 of the NPxY-motif is not conserved. Instead, a conserved stretch of negatively charged amino acids, EEDE279, and two conserved residues P285 and K292 in the flanking region prior to the NPxY-motif are required for CD200R mediated inhibition of p-Erk, pAkt308, p-Akt473, p-rpS6 and LPS-induced IL-8 secretion. Altogether, we show that instead of the more common NPxY-motif, CD200R signaling can be assigned to a unique signaling motif in mammals defined by: EEDExxPYxxYxxKxNxxY.
UR - http://www.scopus.com/inward/record.url?scp=85103573470&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0244770
DO - 10.1371/journal.pone.0244770
M3 - Article
C2 - 33780466
AN - SCOPUS:85103573470
SN - 1932-6203
VL - 16
JO - PLoS ONE
JF - PLoS ONE
IS - 3
M1 - e0244770
ER -