The SphK1/S1P axis regulates morphology and cell-cell interactions of retina pigment epithelium cells
Year: 2025
Type: article
Abstract: Sphingosine-1-phosphate (S1P), a bioactive sphingolipid, regulates multiple key cellular processes. We demonstrated that S1P promotes migration and proinflammatory cytokine release in retinal pigment epithelium (RPE) cells. These cells provide the retina with a physical and metabolic barrier, the disruption of which contributes to the onset of numerous retinopathies. We now investigated whether S1P controlled RPE morphology and cell-cell interactions. Treatment of human RPE cell line (ARPE-19) cultures with PF543, a sphingosine kinase-1 (SphK1) inhibitor, decreased cell migration in confluent cultures. In sub-confluent cultures, PF543 induced cell retraction and the occurrence of elongated, spindle-like cells, absent in controls. PF543 induced similar morphological changes in D407 RPE cell line. S1P preserved cell morphology in PF543-treated cultures, reducing the presence of spindle-like cells. Clusters of paxillin and talin, focal adhesion components, virtually disappeared from cell periphery in PF543-treated cells but were preserved upon S1P addition. While PF543 decreased fibronectin expression and promoted ZO-1 delocalization from the cell membranes, S1P prevented these changes. Pretreatment with W146 and JTE013, S1P1 and S1P2 antagonists, respectively, before adding PF543 and S1P, partially blocked S1P preservation of cell morphology, whereas incubation with BML-241, a S1P3 antagonist, had no effect, implying that activation of S1P1 and S1P2 was required for S1P effect. In control cells, morphology was not affected either by the addition of S1P1, S1P2 and S1P3 antagonists or by inhibiting the export of S1P with an inhibitor for Spinster-2, its major transporter, suggesting that endogenous S1P preservation of morphology did not involve ‘inside-out’ signaling. Our results suggest that SphK1 activity and exogenous S1P were required for controlling RPE cytoskeletal changes and cell interactions, essential for preserving its barrier function. • Sphingosine kinase-1 inhibition alters RPE cell morphology and cellular contacts. • S1P is required for the assembly of focal adhesions and tight junctions. • Exogenous S1P signaling through S1P1 and S1P2 preserve cell morphology and interactions of RPE cells. • Endogenous S1P acts a second messenger to modulate RPE cytoskeletal changes.
Source: Heliyon
Authors: Camila Torlaschi, Gabriela M. Gutiérrez Jofré, Nora P. Rotstein, M. Victoria Simón
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,270
OpenAlex ID: W4414055860