دورية أكاديمية

NAD + -boosting molecules suppress mast cell degranulation and anaphylactic responses in mice.

التفاصيل البيبلوغرافية
العنوان: NAD + -boosting molecules suppress mast cell degranulation and anaphylactic responses in mice.
المؤلفون: Kim HW; Korea Zoonosis Research Institute, Chonbuk National University, Iksan 54596, Republic of Korea., Ryoo GH; Department of Biochemistry and Molecular Biology, Chonbuk National University Medical School, Jeonju 54896, Republic of Korea., Jang HY; Department of Biochemistry and Molecular Biology, Chonbuk National University Medical School, Jeonju 54896, Republic of Korea., Rah SY; Department of Biochemistry and Molecular Biology, Chonbuk National University Medical School, Jeonju 54896, Republic of Korea., Lee DH; Department of Obstetrics and Gynecology, Chonbuk National University Medical School, Jeonju 54896, Republic of Korea., Kim DK; Korea Zoonosis Research Institute, Chonbuk National University, Iksan 54596, Republic of Korea., Bae EJ; College of Pharmacy, Chonbuk National University, Jeonju 54896, Republic of Korea., Park BH; Department of Biochemistry and Molecular Biology, Chonbuk National University Medical School, Jeonju 54896, Republic of Korea.
المصدر: Theranostics [Theranostics] 2022 Apr 11; Vol. 12 (7), pp. 3316-3328. Date of Electronic Publication: 2022 Apr 11 (Print Publication: 2022).
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Ivyspring International Publisher Country of Publication: Australia NLM ID: 101552395 Publication Model: eCollection Cited Medium: Internet ISSN: 1838-7640 (Electronic) Linking ISSN: 18387640 NLM ISO Abbreviation: Theranostics Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Wyoming, N.S.W. : Ivyspring International Publisher, 2011-
مواضيع طبية MeSH: Anaphylaxis*/drug therapy , Sirtuins*/pharmacology, Animals ; Cell Degranulation ; Humans ; Male ; Mast Cells ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; NAD ; Prostate-Specific Antigen
مستخلص: Nicotinamide adenine dinucleotide (NAD + ) acts as a cofactor for multiple biological processes. While previous research has revealed that the NAD + declines associated with aging contributes to an impairment of immune cells, its role in mast cell function, especially in response to an anaphylactic condition, has remained unexplored. We tested whether the restoration of cellular NAD + concentration by the supplementation of NAD + boosting molecules prevented mast cell degranulation and anaphylactic responses. Methods: Bone marrow derived mast cells (BMMCs) and human cord blood derived mast cells were treated with NAD + precursors nicotinamide mononucleotide (NMN) and nicotinamide riboside (NR), and FcεRI downstream signaling was assessed. Animal models of passive systemic anaphylaxis (PSA) and passive cutaneous anaphylaxis (PCA) were used to investigate the effects of NAD + precursors in the anaphylactic responses of mice. Results: Treatment of murine BMMCs and human cord blood derived mast cells with NAD + precursors repressed intracellular signaling downstream of FcεRI, as well as the release of inflammatory cytokines and lipid mediators. The intraperitoneal administration of NMN or NR also markedly attenuated IgE-mediated anaphylactic responses in mouse models of PSA and PCA. These beneficial effects of NAD + precursors, however, were attenuated in mast cell-specific Sirt6 knockout mice, indicating a Sirt6 dependency for their action. Conclusion: NAD + precursors may serve as an effective therapeutic strategy that limits mast cell-mediated anaphylactic responses.
Competing Interests: Competing Interests: The authors have declared that no competing interest exists.
(© The author(s).)
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فهرسة مساهمة: Keywords: NMN; NR; Sirt6; anaphylaxis; mast cell
المشرفين على المادة: 0U46U6E8UK (NAD)
EC 2.4.2.31 (Sirt6 protein, mouse)
EC 3.4.21.77 (Prostate-Specific Antigen)
EC 3.5.1.- (SIRT6 protein, human)
EC 3.5.1.- (Sirtuins)
تواريخ الأحداث: Date Created: 20220513 Date Completed: 20220517 Latest Revision: 20220716
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC9065190
DOI: 10.7150/thno.69684
PMID: 35547746
قاعدة البيانات: MEDLINE