Signaling of type II oncostatin M receptor

Oncostatin M (OSM), mediates its bioactivities through two different heterodimer receptors. They both involve the gp130-transducing receptor, which dimerizes with either leukemia inhibitor receptor beta or with OSM receptor beta (OSMR beta) to generate, respectively, type I and type II OSM receptors. Co-precipitation of gp130-associated proteins, flow cytometry, polymerase chain reaction, and tyrosine phosphorylation analyses allowed the characterization of both types of OSM receptors expressed on the surface of different cell lines, It also allowed the detection of a large size protein, p250, that specifically associates to the type II OSM receptor components anti that is tyrosine-phosphorylated after the activation peak of the gp130.OSMR beta heterocomplex, The restricted expression of type I OSM receptor by the SAR choriocarcinoma cell line, and type II receptor by the A375 melanoma cell line, permitted the characterization of their signaling machineries. Both type I and type II OSM receptors activated Jak1, Jak2, and Tyk2 receptor-associated tyrosine kinases, The information is nest relayed to the nucleus by the STAT3 transcriptional activator, which is recruited by both types of OSM receptors, In addition, STAT5b was specifically activated through the gp120.OSMR beta type II heterocomplex. The signaling pathway differences observed between the common type I LIF/OSM receptor and the specific type II OSM receptor might explain some of the bioactivities specifically displayed by OSM.