28
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The Multi-faceted Ecto-enzyme CD38: Roles in Immunomodulation, Cancer, Aging, and Metabolic Diseases

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          CD38 (Cluster of Differentiation 38) is a multifunctional ecto-enzyme that metabolizes NAD+ and mediates nicotinamide dinucleotide (NAD+) and extracellular nucleotide homeostasis as well as intracellular calcium. CD38 is also an emerging therapeutic target under conditions in which metabolism is altered including infection, aging, and tumorigenesis. We describe multiple enzymatic activities of CD38, which may explain the breadth of biological roles observed for this enzyme. Of greatest significance is the role of CD38 as an ecto-enzyme capable of modulating extracellular NAD+ precursor availability: 1 to bacteria unable to perform de novo synthesis of NAD+; and 2 in aged parenchyma impacted by the accumulation of immune cells during the process of ‘inflammaging’. We also discuss the paradoxical role of CD38 as a modulator of intracellular NAD+, particularly in tumor immunity. Finally, we provide a summary of therapeutic approaches to CD38 inhibition and ‘NAD+ boosting’ for treatment of metabolic dysfunction observed during aging and in tumor immunity. The present review summarizes the role of CD38 in nicotinamide nucleotide homeostasis with special emphasis on the role of CD38 as an immunomodulator and druggable target.

          Related collections

          Most cited references92

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          T cell metabolism drives immunity

          Buck et al. discuss the role of lymphocyte metabolism on immune cell development and function.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Targeting CD38 with Daratumumab Monotherapy in Multiple Myeloma.

            Multiple myeloma cells uniformly overexpress CD38. We studied daratumumab, a CD38-targeting, human IgG1κ monoclonal antibody, in a phase 1-2 trial involving patients with relapsed myeloma or relapsed myeloma that was refractory to two or more prior lines of therapy.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Mitochondrial transfer between cells can rescue aerobic respiration.

              Current theory indicates that mitochondria were obtained 1.5 billion years ago from an ancient prokaryote. The mitochondria provided the capacity for aerobic respiration, the creation of the eukaryotic cell, and eventually complex multicellular organisms. Recent reports have found that mitochondria play essential roles in aging and determining lifespan. A variety of heritable and acquired diseases are linked to mitochondrial dysfunction. We report here that mitochondria are more dynamic than previously considered: mitochondria or mtDNA can move between cells. The active transfer from adult stem cells and somatic cells can rescue aerobic respiration in mammalian cells with nonfunctional mitochondria.
                Bookmark

                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                31 May 2019
                2019
                : 10
                : 1187
                Affiliations
                Signal Transduction and Molecular Nutrition Laboratory, Kogod Center on Aging, Department of Anesthesiology and Perioperative Medicine, Mayo Clinic College of Medicine , Rochester, MN, United States
                Author notes

                Edited by: Silvia Deaglio, University of Turin, Italy

                Reviewed by: Antje Garten, Leipzig University, Germany; Yasser Mohamed El-Sherbiny, Nottingham Trent University, United Kingdom

                *Correspondence: Eduardo N. Chini chini.eduardo@ 123456mayo.edu

                This article was submitted to Inflammation, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2019.01187
                6555258
                31214171
                538cae03-d622-4bcd-beef-3b694461acc4
                Copyright © 2019 Hogan, Chini and Chini.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 April 2019
                : 10 May 2019
                Page count
                Figures: 6, Tables: 1, Equations: 0, References: 111, Pages: 12, Words: 8227
                Funding
                Funded by: Mayo Foundation for Medical Education and Research 10.13039/100007048
                Categories
                Immunology
                Review

                Immunology
                cd38,nadase,nad+,aging,cancer,metabolism,senescence,macrophages
                Immunology
                cd38, nadase, nad+, aging, cancer, metabolism, senescence, macrophages

                Comments

                Comment on this article