Sphingosine 1-phosphate signaling axis mediates neuropeptide S-induced invasive phenotype of endometriotic cells.

Abstract

Endometriosis is a chronic gynecological syndrome characterized by endometrial cell invasion of the extra-uterine milieu, pelvic pain and infertility. Treatment relies on either symptomatic drugs or hormonal therapies, even though the mechanism involved in the onset of endometriosis is yet to be elucidated. The signaling of sphingolipid sphingosine 1-phosphate (S1P) is profoundly dysregulated in endometriosis. Indeed, sphingosine kinase (SK)1, one of the two isoenzymes responsible for S1P biosynthesis, and S1P1, S1P3 and S1P5, three of its five specific receptors, are more highly expressed in endometriotic lesions compared to healthy endometrium. Recently, missense coding variants of the gene encoding the receptor 1 for neuropeptide S (NPS) have been robustly associated with endometriosis in humans. This study aimed to characterize the biological effect of NPS in endometriotic epithelial cells and the possible involvement of the S1P signaling axis in its action. NPS was found to potently induce cell invasion and actin cytoskeletal remodeling. Of note, the NPS-induced invasive phenotype was dependent on SK1 and SK2 as well as on S1P1 and S1P3, given that the biological action of the neuropeptide was fully prevented when one of the two biosynthetic enzymes or one of the two selective receptors was inhibited or silenced. Furthermore, the RhoA/Rho kinase pathway, downstream to S1P receptor signaling, was found to be critically implicated in invasion and cytoskeletal remodeling elicited by NPS. These findings provide new information to the understanding of the molecular mechanisms implicated in endometriosis pathogenesis, establishing the rationale for non-hormonal therapeutic targets for its treatment.

• Authors: Matteo Prisinzano, Caterina Bernacchioni, Isabelle Seidita, Margherita Rossi, Maryam Raeispour, Francesca Cencetti, Silvia Vannuccini, Massimiliano Fambrini, Felice Petraglia, Paola Bruni, Chiara Donati
• Journal: The FEBS journal (FEBS J) Vol. 291 Issue 8 Pg. 1744-1758 (Apr 2024) ISSN: 1742-4658 [Electronic] England
• PMID: 38287231 (Publication Type: Journal Article)
• Copyright: © 2024 Federation of European Biochemical Societies.

Chemical References

• Lysophospholipids
• Receptors, Lysosphingolipid
• Sphingosine
• sphingosine 1-phosphate
• neuropeptide S, human

Topics

• Female
• Humans
• Endometriosis (genetics)
• Lysophospholipids (metabolism)
• Phenotype
• Receptors, Lysosphingolipid (genetics, metabolism)
• Sphingosine (metabolism, analogs & derivatives)