Visualizing S1P-directed cellular egress by intravital imaging

Biochim Biophys Acta. 2014 May;1841(5):738-44. doi: 10.1016/j.bbalip.2013.09.012. Epub 2013 Oct 1.

Abstract

Sphingosine-1-phosphate (S1P) is a bioactive lipid that provides cellular signals through plasma membrane G protein-coupled receptors. The S1P receptor signaling system has a fundamental and widespread function in licensing the exit and release of hematopoietically derived cells from various tissues into the circulation. Although the outlines of the mechanism have been established through genetic and pharmacologic perturbations, the temporal and spatial dynamics of the cellular events involved have been unclear. Recently, two-photon intravital imaging has been applied to living tissues to visualize the cellular movements and interactions that occur during egress processes. Here we discuss how some of these recent findings provide a clearer picture regarding S1P receptor signaling in modulating cell egress into the circulation. This article is part of a Special Issue entitled New Frontiers in Sphingolipid Biology.

Keywords: Gradient; Receptor; Signaling; Sphingolipid; Sphingosine-1-phosphate; Two-photon microscopy.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • Cell Membrane / metabolism
  • Cell Physiological Phenomena*
  • Humans
  • Lysophospholipids / metabolism*
  • Microscopy, Fluorescence, Multiphoton / methods*
  • Molecular Imaging / methods*
  • Receptors, Lysosphingolipid / metabolism
  • Signal Transduction
  • Sphingosine / analogs & derivatives*
  • Sphingosine / metabolism

Substances

  • Lysophospholipids
  • Receptors, Lysosphingolipid
  • sphingosine 1-phosphate
  • Sphingosine