Characterization of novel store-operated calcium entry effectors

• Published in: Biochimica et biophysica acta 2014-10, Vol.1843 (10), p.2341-2347
• Main Authors: Djillani, Alaeddine, Nüße, Oliver, Dellis, Olivier
• Format: Article
• Language: English
• Subjects: 2-APB; Boron Compounds - chemical synthesis; Boron Compounds - pharmacology; Calcium - analysis; Calcium - metabolism; Calcium Channel Blockers - chemical synthesis; Calcium Channel Blockers - pharmacology; Calcium Channels - metabolism; Calcium Signaling; Drug Design; Enzyme Inhibitors - pharmacology; Fluorescent Dyes; Humans; IL-2; Indoles; Inhibition; Interleukin-2 - biosynthesis; Interleukin-2 - secretion; Ion Transport; Jurkat Cells; Potentiation; Quantitative Structure-Activity Relationship; Spectrometry, Fluorescence; Store-operated calcium entry; Thapsigargin - pharmacology
• ISSN: 0167-4889; 0006-3002; 1879-2596
• DOI: 10.1016/j.bbamcr.2014.03.012

2-Aminoethyl diphenylborinate (2-APB) is a well-known effector of the store-operated Ca2+ entry of several cell types such as immune cells, platelets and smooth muscle cells. 2-APB has a dual effect: potentiation at 1–5μM and inhibition at >30μM. Unfortunately, it is also able to modify the activity of other Ca2+ transporters and, thus, cannot be used as a therapeutic tool to control the leukocyte activity in diseases like inflammation. Previously, we have shown that SOCE potentiation by 2-APB depends on the presence of the central boron-oxygen core (BOC) and that the phenyl groups determine the sensitivity of the molecule to inhibit and/or potentiate the SOCE. We hypothesized that by modifying the two phenyl groups of 2-APB, we could identify more efficient and specific analogues. In fact, the addition of methoxyl groups to one phenyl group greatly decreased the potentiation ability without any significant effect on the inhibition. Surprisingly, when the free rotation of the two phenyl groups was blocked by a new hydrocarbon bridge, the BOC was no longer able to potentiate. Furthermore, larger aryl groups than phenyl also impaired the activity of the BOC. Thus, the potentiation site in the Ca2+ channel is not accessible by the BOC when the lateral groups are too large or unable to freely rotate. However, these molecules are potent inhibitors of store-operated calcium entry with affinities below 1μM, and they can block the activation of the Jurkat T cells. Thus, it is possible to characterize 2-APB analogues with different properties that could be the first step in the discovery of new immunomodulators. This article is part of a special issue entitled “Calcium Signaling in Health and Disease. Guest Editors: Geert Bultynck, Jacques Haiech, Claus W. Heizmann, Joachim Krebs, and Marc Moreau. •The modification of the phenyl groups in 2-APB creates new potent inhibitors of SOCE.•Dibenzothienyl-APB is among the most potent SOCE inhibitors known.•Cyclic-APB and dibenzothienyl-APB do not potentiate SOCE in contrast to 2-APB.•Cyclic-APB and dibenzothienyl-APB strongly inhibit IL-2 synthesis by T lymphocytes.•The structure–function analysis of 2-APB may lead to new immunomodulators.