Activity of nicotinic acid substituted nicotinic acid adenine dinucleotide phosphate (NAADP) analogs in a human cell line: Difference in specificity between human and sea urchin NAADP receptors

Ramadan A. Ali, Tetyana Zhelay, Christopher J. Trabbic, Timothy F. Walseth, James T. Slama, David R. Giovannucci, Katherine A. Wall

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Nicotinic acid adenine dinucleotide phosphate (NAADP) is the most potent Ca2+ mobilizing second messenger that has been identified. We have previously shown that NAADP analogs substituted at the 5-position of nicotinic acid were recognized by the sea urchin receptor at low concentration, whereas the 4- substituted analogs were not as potent. However, to date the structure-activity relationship (SAR) of these analogs has not been addressed in mammalian systems. Thus, we asked whether these structurally modified analogs behave similarly in an NAADP-responsive mammalian cell line (SKBR3) using microinjection and single cell fluorescent imaging methods. Novel "caged" 4- and 5-substituted NAADP analogs that were activated inside the cell by flash photolysis resulted in Ca2+ mobilizing activity in SKBR3 cells in a concentration dependent manner, but with reduced effectiveness compared to unmodified NAADP. The SAR in mammalian SKBR3 cells was quite different from that of sea urchin and may suggest that there are differences between NAADP receptors in different species or tissues. Importantly, these data indicate that modifications at the 4- and 5-position of the nicotinic acid ring may lead to the development of functional photoaffinity labels that could be used for receptor localization and isolation in mammalian systems.

Original languageEnglish (US)
Pages (from-to)93-103
Number of pages11
JournalCell Calcium
Volume55
Issue number2
DOIs
StatePublished - Feb 2014

Bibliographical note

Funding Information:
Thank you to Dr. Surya Nauli for the use of his microinjection apparatus. This work was supported by a University of Toledo Interdisciplinary Research Initiation Program Grant and by NIH Grant # GM100444-01 .

Keywords

  • Antagonists
  • Caged-NAADP
  • NAADP
  • SKBR3 cells
  • Structure-activity relationships

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