Measurement of neutral ceramidase activity in vitro and in vivo

Anal Biochem. 2022 Apr 15:643:114577. doi: 10.1016/j.ab.2022.114577. Epub 2022 Feb 5.

Abstract

Neutral ceramidase is a hydrolase of ceramide that has been implicated in multiple biologic processes, including inflammation and oncogenesis. Ceramides and other sphingolipids, belong to a family of N-acyl linked lipids that are biologically active in signaling, despite their limited structural functions. Ceramides are generally pro-apoptotic, while sphingosine and sphingosine-1-phosphate (S1P) exert proliferative and pro-oncogenic effects. Ceramidases are important regulators of ceramide levels that hydrolyze ceramide to sphingosine. Thus, ceramidase inhibition significantly increases the quantities of ceramide and its associated signaling. To better understand the function of ceramide, biochemical and cellular assays for enzymatic activity were developed and validated to identify inhibitors of human neutral ceramidase (nCDase). Here we review the measurement of nCDase activity both in vitro and in vivo.

Keywords: Ceramides; Neutral ceramidase; Neutral ceramidase enzymatic assays.

Publication types

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

MeSH terms

  • Humans
  • Neutral Ceramidase / analysis*
  • Neutral Ceramidase / genetics
  • Neutral Ceramidase / metabolism
  • Pseudomonas aeruginosa / enzymology

Substances

  • Neutral Ceramidase