Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Apr;237(4):2064-2077.
doi: 10.1002/jcp.30688. Epub 2022 Jan 30.

Adenosine diphosphate ribose cyclase: An important regulator of human pathological and physiological processes

Affiliations
Review

Adenosine diphosphate ribose cyclase: An important regulator of human pathological and physiological processes

Feng Zeng et al. J Cell Physiol. 2022 Apr.

Abstract

Adenosine diphosphate ribose cyclase (ADPRC) exists widely in eukaryotes and lower metazoans cells. It can degrade nicotinamide adenine dinucleotide (NAD) into cyclic ADP ribose (cADPR) and nicotinamide, and subsequently hydrolyses cADPR to ADP ribose (ADPR). In this paper, we have summarized the relative subcellular localization of ADPRC and enzymes with ADPRC activity in organisms, related enzyme family members of ADPRC are also described. In addition, we discussed the main biological functions of ADPRC, the regulation of Ca2+ signal, the regulation of insulin and glucagon secretion, oxytocin secretion, and the effects of renal and pulmonary vasomotor tension. Finally, we expounded the relationship between ADPRC and human health and disease occurrence. It provides a theoretical basis for the targeted treatment of ADPRC as a pharmacological tool for related diseases, and has important significance in clinical diagnosis and disease intervention.

Keywords: ADPR cyclase; cell signaling; pathology; physiology; signal transduction pathways.

PubMed Disclaimer

References

REFERENCES

    1. Abdul-Awal, S., Hotta, C. T., Davey, M. P., Dodd, A. N., Smith, A. G., & Webb, A. A. (2016). NO-mediated [Ca2+] cyt increases depend on ADP-ribosyl cyclase activity in Arabidopsis. Plant Physiology, 171(1), 623-631. https://doi.org/10.1104/pp.15.01965
    1. Adebanjo, O. A., Anandatheerthavarada, H. K., Koval, A. P., Moonga, B. S., Biswas, G., Sun, L., & Epstein, S. (1999). A new function for CD38/ADP-ribosyl cyclase in nuclear Ca2+ homeostasis. Nature Cell Biology, 1(7), 409-414. https://doi.org/10.1038/15640
    1. Baum, N., Fliegert, R., Bauche, A., Hambach, J., Menzel, S., Haag, F., & Koch-Nolte, F. (2021). Daratumumab and nanobody-based heavy chain antibodies inhibit the ADPR cyclase but not the NAD+ hydrolase activity of CD38-expressing multiple myeloma cells. Cancers, 13(1), 76. https://doi.org/10.3390/cancers13010076
    1. Bezin, S., Charpentier, G., Lee, H. C., Baux, G., Fossier, P., & Cancela, J.-M. (2008). Regulation of nuclear Ca2+ signaling by translocation of the Ca2+ messenger synthesizing enzyme ADP-ribosyl cyclase during neuronal depolarization. Journal of Biological Chemistry, 283(41), 27859-27870. https://doi.org/10.1074/jbc.M804701200
    1. Burel, J. G., Apte, S. H., Groves, P. L., Klein, K., McCarthy, J. S., & Doolan, D. L. (2016). Reduced plasmodium parasite burden associates with CD38+ CD4+ T cells displaying cytolytic potential and impaired IFN-γ production. PLOS Pathogens, 12(9), e1005839. https://doi.org/10.1371/journal.ppat.1005839

LinkOut - more resources