A non-voltage-gated calcium channel withL-type characteristics activated by B cell receptor ligation

Gillian Grafton, Leanne Stokes, Kai-Michael Toellner, John Gordon

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32 Citations (Scopus)


In mature B cells engagement of the antigen-receptor (BCR) results in a peak of Ca2+ from mobilisation of internal stores followed by a lower but sustained elevation that is dependent upon extracellular Ca2+. The Ca2+ channel involved in the sustained elevation remains uncharacterised. Here we have presented evidence that although non-excitable, B cells expressed a BCR-activated Ca2+ channel sharing some properties of conventional L-type voltage-gated channels. Human lymphoma B cells expressed a transcript having homology to a highly conserved region on the pore-forming alpha(1.2) subunit of L-type voltage-gated Ca2+ channels. The alpha(1.2) protein was expressed together with the beta1 subunit, while an antibody raised against the extracellular portion of L-type Ca2+ channels caused a Ca2+ flux in these cells. Drugs that block classical L-type channels abolished the BCR-induced Ca2+ flux while directly activating a plasma membrane Ca2+ channel: activation of the channel, separate from Ca2+ influx, inhibited BCR-induced Ca2+ release from intracellular stores. BAYK8644-a drug that binds to open L-type channels-failed to release intracellular Ca2+ in the absence of BCR cross-linking but instantly abolished the BCR-induced Ca2+ peak and established the sustained phase of the response. The BCR-activated calcium channel appeared to terminate the initial peak of BCR-induced Ca2+ release and initiate the sustained phase of the signal. (C) 2003 Elsevier Inc. All rights reserved.
Original languageEnglish
Pages (from-to)2001-09
Number of pages9
JournalBiochemical Pharmacology
Publication statusPublished - 15 Nov 2003


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