Table 1.
Pathophysiological functions of LysoPS receptors
| Receptor | Experiment | Model or cell-types | Functions | Refs. |
|---|---|---|---|---|
| GPR34/LPS1 | In vivo | DTH model | Suppress pro-inflammatory cytokine production | [43] |
| In vivo | Fungal infection model | Promote fungal clearance | [43] | |
| In vivo | Neuropathic pain model | Enhance microglial pro-inflammatory responses | [46] | |
| In vitro | Primary microglia | Promote phagocytosis | [45] | |
| In vitro | Cervical cancer cell gastric cancer cell colorectal cancer cell | Promote cellular invasion and proliferation | [47, 48] | |
| P2Y10/LPS2 | In vitro | Primary dendritic cell, microglia | Suppress cytokine production | [7] |
| In vitro | Primary eosinophil | Promote degranulation, survival, and formation of EET | [5, 8] | |
| GPR174/LPS3 | In vivo | EAE model sepsis model | Attenuate disease severity by suppressing Treg cell function | [3] |
| In vivo in vitro | Primary CD4 T cell | Suppress IL-2 production | [6] | |
| In vivo | Splenic follicular B cell | Inhibit the cellular migration into the follicle center | [9] | |
| In vivo | Splenic marginal zone B cell | Inhibit the inflammatory responses, proliferation, and differentiation | [11, 4] |