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of Biomedicine, University of Baselhttps://www.ebi.ac.uk/ena/browser/view/PRJNA641170Mus musculusPurpose: Our previous experiments showed that LPA activated inhibitory G-protein signaling in human GPR35-transfected cells. We wanted to test the LPA signaling in presence or absence of GPR35. Methods: We isolated RNA from bone-marrow derived macrophages (BMDMs) from WT or GPR35-deficient mice that were treated with LPA or LPS, and left untreated for control. Results: We have found that GPR35-deficiency alters the transcriptional profiles in response to LPA in BMDMs. On the other hand, LPS-treated WT and GPR35-deficient BMDMs showed similar transcriptional changes. Conclusion: GPR35-deficientcy alters the LPA but not LPS signaling. Overall design: mRNA profiles of cont, LPA- or LPS-treated WT or GPR35-deficient BMDMsxref:PubMed:32755573ENAfalseGPR35 mediates lysophosphatidic acid-signaling in bone marrow-derived macrophages at the transcriptional levelGPR35 mediates lysophosphatidic acid-signaling in bone marrow-derived macrophages at the transcriptional level2025-09-242020-06-24PRJNA641170GSE1530121009032755573