Dysregulated sphingolipid metabolism in endometriosis

J Clin Endocrinol Metab. 2014 Oct;99(10):E1913-21. doi: 10.1210/jc.2014-1340. Epub 2014 Jun 24.

Abstract

Background: In endometriosis, the establishment and subsistence of ectopic lesions outside the endometrium suggest an altered cellular state for pathological hyperplasia. Sphingolipids are bioactive compounds, and their biosynthesis and metabolism modulate a range of cellular processes including proliferation, migration and apoptosis. We demonstrate that aberrations in sphingolipid metabolism occur in women with endometriosis.

Methods: Targeted mass spectrometry on >120 sphingolipids were measured in the sera (n = 62), peritoneal fluid (n = 63), and endometrial tissue (n = 14) of women with and without endometriosis. Quantitative RT-PCR and immunohistochemistry were performed on endometrial tissues determine the expression levels of sphingolipid enzymes.

Results: Sphingolipidomics identified the in vivo accumulation of numerous sphingolipids, including the functionally antagonistic glucosylceramides and ceramides in the serum and PF of women with endometriosis. We found upregulation of specific sphingolipid enzymes, namely sphingomyelin synthase 1 (SMS1), sphingomyelinase 3 (SMPD3), and glucosylceramide synthase (GCS) in the endometrium of endometriotic women with corresponding increased GlcCer, decreased sphingomyelin levels, and decreased apoptosis in the endometrium.

Conclusions: Our sphingolipidomics approach provided evidence of altered sphingolipid metabolism flux in serum, peritoneal fluid, and endometrial tissue in women with endometriosis. The results provide new information on how sphingolipids and eutopic endometrium may contribute to the pathophysiology of endometriosis. The results also have implications for the use of sphingolipids as potential biomarkers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / physiology
  • Ascitic Fluid / metabolism
  • Cell Movement / physiology
  • Cell Proliferation
  • Endometriosis / enzymology*
  • Endometriosis / pathology
  • Female
  • Glucosyltransferases / genetics
  • Glucosyltransferases / metabolism*
  • Humans
  • Infertility, Female / genetics
  • Infertility, Female / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Middle Aged
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Peritoneal Diseases / genetics
  • Peritoneal Diseases / metabolism
  • Sphingolipids / biosynthesis
  • Sphingolipids / blood
  • Sphingolipids / metabolism*
  • Sphingomyelin Phosphodiesterase / genetics
  • Sphingomyelin Phosphodiesterase / metabolism*
  • Transferases (Other Substituted Phosphate Groups) / genetics
  • Transferases (Other Substituted Phosphate Groups) / metabolism*
  • Young Adult

Substances

  • Membrane Proteins
  • Nerve Tissue Proteins
  • Sphingolipids
  • Glucosyltransferases
  • ceramide glucosyltransferase
  • SGMS1 protein, human
  • Transferases (Other Substituted Phosphate Groups)
  • SMPD3 protein, human
  • Sphingomyelin Phosphodiesterase

Grants and funding

This work was supported by the Singapore National Research Foundation (to Singapore-MIT Alliance for Research and Technology). J.K.Y.C. received salary support from the National Medical Research Council (CSA/043/2012).