TSLP induced by estrogen stimulates secretion of MCP-1 and IL-8 and growth of human endometrial stromal cells through JNK and NF-κB signal pathways

Int J Clin Exp Pathol. 2014 Apr 15;7(5):1889-99. eCollection 2014.

Abstract

It has reported that human endometrial stromal cells (ESCs) express thymic stromal lymphopoietin (TSLP), and TSLP concentrations in the serum and peritoneal fluid were higher in women with endometriosis. Endometriosis is an estrogen-dependent disease. The present study aimed to elucidate whether and how estrogen regulates the growth of ESCs through TSLP. The ESCs behaviors in vitro were verified by SRB assay and Ki67 level detection, respectively. In addition, the effects of estrogen on TSLP and TSLP on the correspondent functional molecules were investigated by ELISA and flow cytometry. Here we found that estrogen stimulated the secretion of TSLP in a dosage-dependent manner. Recombinant human TSLP stimulates the secretion of MCP-1 and IL-8, and markedly promotes the viability and proliferation relative gene Ki-67 expression of ESCs. These effects could be abolished by the inhibitor for JNK or NF-κB signal, respectively. Moreover, not only anti-TSLP neutralizing antibody, but also blocking JNK or NF-κB signal by inhibitor abrogated the stimulatory role in the production of MCP-1 and IL-8, and the growth of ESCs induced by estrogen. Our current study has demonstrated that TSLP is involved in the regulation of estrogen on the secretion of MCP-1 and IL-8, and the growth of ESCs through JNK and NF-κB signal pathways, which suggests that the abnormal high expression of TSLP induced by estrogen may play an important role in ESCs growth and finally contribute to the origin and development of endometriosis.

Keywords: ESCs; IL-8; MCP-1; TSLP; endometriosis; estrogen; proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell Proliferation / drug effects*
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chemokine CCL2 / metabolism*
  • Cytokines / metabolism*
  • Dose-Response Relationship, Drug
  • Endometriosis / immunology
  • Endometriosis / metabolism*
  • Endometriosis / pathology
  • Endometrium / drug effects*
  • Endometrium / immunology
  • Endometrium / metabolism
  • Endometrium / pathology
  • Estradiol / pharmacology*
  • Female
  • Humans
  • Interleukin-8 / metabolism*
  • JNK Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Ki-67 Antigen / metabolism
  • Middle Aged
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / metabolism*
  • Ovarian Diseases / immunology
  • Ovarian Diseases / metabolism*
  • Ovarian Diseases / pathology
  • Protein Kinase Inhibitors / pharmacology
  • Signal Transduction / drug effects
  • Stromal Cells / drug effects*
  • Stromal Cells / immunology
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Thymic Stromal Lymphopoietin
  • Up-Regulation
  • Young Adult

Substances

  • CCL2 protein, human
  • CXCL8 protein, human
  • Chemokine CCL2
  • Cytokines
  • Interleukin-8
  • Ki-67 Antigen
  • NF-kappa B
  • Protein Kinase Inhibitors
  • Estradiol
  • JNK Mitogen-Activated Protein Kinases
  • Thymic Stromal Lymphopoietin