Involvement of ryanodine receptors in sphingosylphosphorylcholine-induced calcium release from brain microsomes
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Sphingolipid-mediated calcium signaling and its pathological effects
2018, Biochimica et Biophysica Acta - Molecular Cell ResearchRegulation of ryanodine receptors by sphingosylphosphorylcholine: Involvement of both calmodulin-dependent and -independent mechanisms
2010, Biochemical and Biophysical Research CommunicationsCitation Excerpt :Our current results are also consistent with our former data suggesting that SPC can dissociate the complex between RyRs and CaM, and we have found that the presence of CaM can modify the direct inhibitory effect of SPC on the channel. On the other hand, an involvement of RyRs in SPC-induced Ca2+ release from brain microsomes has been reported [9]. Hence, we studied RyR activity similarly as these authors had, isolating microsomes from bovine brain cerebrum by differential centrifugation, loading these with Ca2+ in presence of an ATP-regenerating system, and measuring Ca2+ release using a fluorescent Ca2+ indicator.
Dissociation of calmodulin-target peptide complexes by the lipid mediator sphingosylphosphorylcholine: Implications in calcium signaling
2010, Journal of Biological ChemistryCitation Excerpt :Next, to investigate the specificity of the complex-dissociating effect of SPC regarding the peptide, and also to assess its possible functional consequences, we studied the interaction between the CaM-binding domain of RyR1 and CaM. We chose this peptide because SPC has previously been suggested to be involved in regulation of RyRs (15, 26), and also because calcium binding to CaM leads to an N-terminal shift in its binding site on the peptide (29). Thus, this peptide is unique in a way that it binds constitutively to either apo- or Ca2+-saturated CaM, so it is a convenient tool to study the effect of SPC on the apoCaM-target interaction as well.
The multi-functional role of sphingosylphosphorylcholine
2008, Progress in Lipid ResearchThe pathogenesis of glycosphingolipid storage disorders
2004, Seminars in Cell and Developmental Biology