Abstract

Sphingosine kinase 2 (SK2) is a ubiquitously expressed lipid kinase that has important, albeit complex and poorly understood, roles in regulating cell survival and cell death. In addition to being able to promote cell cycle arrest and apoptosis under certain conditions, it has recently been shown that SK2 can promote neoplastic transformation and tumorigenesis in vivo. Therefore, well validated and reliable tools are required to study and better understand the true functions of SK2. Here, we compare two commercially available SK2 antibodies: a rabbit polyclonal antibody from Proteintech that recognizes amino acids 266-618 of human SK2a, and a rabbit polyclonal antibody from ECM Biosciences that recognizes amino acids 36-52 of human SK2a. We examine the performance of these antibodies for use in immunoblotting, immunoprecipitation and immunofluorescence staining of endogenous SK2, using human HEK293 and HeLa cell lines, as well as mouse embryonic fibroblasts (MEFs). Furthermore, we assess the specificity of these antibodies to the target protein through the use of siRNA-mediated SK2 knockdown and SK2 knockout ( Sphk2-/-) MEFs. Our results demonstrate that the Proteintech anti-SK2 antibody reproducibly displayed superior sensitivity and selectivity towards SK2 in immunoblot analyses, while the ECM Biosciences anti-SK2 antibody was reproducibly superior for SK2 immunoprecipitation and detection by immunofluorescence staining. Notably, both antibodies produced non-specific bands and staining in the MEFs, which was not observed with the human cell lines. Therefore, we conclude that the Proteintech SK2 antibody is a valuable reagent for use in immunoblot analyses, and the ECM Biosciences SK2 antibody is a useful tool for SK2 immunoprecipitation and immunofluorescence staining, at least in the human cell lines employed in this study.

Highlights

  • Sphingolipids are an important family of cellular molecules that form critical structural components of cell membranes, as well as performing numerous signaling functions[1]

  • Some faint non-specific bands were detected in both the WT and Sphk2-/- mouse embryonic fibroblasts (MEFs) lysates by this antibody, which were not observed in the human cell lines

  • The ECM Biosciences anti-Sphingosine kinase 2 (SK2) antibody did not appear to be very sensitive towards SK2, as no band was detected at the expected size in the HeLa lysates, and only very faint bands were present in the

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Summary

Introduction

Sphingolipids are an important family of cellular molecules that form critical structural components of cell membranes, as well as performing numerous signaling functions[1]. Of the many enzymes responsible for the biosynthesis and metabolism of sphingolipids, the sphingosine kinases (SKs) are of particular interest to study as they catalyze the formation of sphingosine 1-phosphate (S1P), and in doing so can promote cell survival, proliferation, migration and angiogenesis[2]. Both sphingosine kinases, SK1 and SK2, have been shown to be upregulated in various human cancers and both have documented roles in mediating oncogenesis[3,4]. The mechanisms regulating the localization and functions of SK2, allowing it to switch between pro-apoptotic and pro-survival under certain conditions, remain poorly understood

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