| First Author | Shanmugam A | Year | 2015 |
| Journal | J Neurochem | Volume | 132 |
| Issue | 5 | Pages | 546-58 |
| PubMed ID | 25439327 | Mgi Jnum | J:219837 |
| Mgi Id | MGI:5629805 | Doi | 10.1111/jnc.13002 |
| Citation | Shanmugam A, et al. (2015) Sigma receptor 1 activation attenuates release of inflammatory cytokines MIP1gamma, MIP2, MIP3alpha, and IL12 (p40/p70) by retinal Muller glial cells. J Neurochem 132(5):546-58 |
| abstractText | The high-affinity sigma receptor 1 (sigmaR1) ligand (+)-pentazocine ((+)-PTZ) affords profound retinal neuroprotection in vitro and in vivo by a yet-unknown mechanism. A common feature of retinal disease is Muller cell reactive gliosis, which includes cytokine release. Here, we investigated whether lipopolysaccharide (LPS) stimulates cytokine release by primary mouse Muller cells and whether (+)-PTZ alters release. Using a highly sensitive inflammatory antibody array we observed significant release of macrophage inflammatory proteins (MIP1gamma, MIP2, MIP3alpha) and interleukin-12 (IL12 (p40/p70)) in LPS-treated cells compared to controls, and a significant decrease in secretion upon (+)-PTZ treatment. Muller cells from sigmaR1 knockout mice demonstrated increased MIP1gamma, MIP2, MIP3alpha and IL12 (p40/p70) secretion when exposed to LPS compared to LPS-stimulated WT cells. We investigated whether cytokine secretion was accompanied by cytosolic-to-nuclear NFkappaB translocation and whether endothelial cell adhesion/migration was altered by released cytokines. Cells exposed to LPS demonstrated increased NFkappaB nuclear location, which was reduced significantly in (+)-PTZ-treated cells. Media conditioned by LPS-stimulated-Muller cells induced leukocyte-endothelial cell adhesion and endothelial cell migration, which was attenuated by (+)-PTZ treatment. The findings suggest that release of certain inflammatory cytokines by Muller cells can be attenuated by sigmaR1 ligands providing insights into the retinal neuroprotective role of this receptor. |
