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TNAP 在慢性炎症和代谢中的新作用。

TNAP as a New Player in Chronic Inflammatory Conditions and Metabolism.

机构信息

Bernhard-Heine-Center for Locomotion Research, Department of Orthopedics, Julius-Maximilians-University Würzburg, 97076 Würzburg, Germany.

Institute for Human Genetics, Biocenter, Julius-Maximilians-University Würzburg, 97074 Würzburg, Germany.

出版信息

Int J Mol Sci. 2021 Jan 18;22(2):919. doi: 10.3390/ijms22020919.

DOI:10.3390/ijms22020919
PMID:33477631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7831495/
Abstract

This review summarizes important information on the ectoenzyme tissue-nonspecific alkaline phosphatase (TNAP) and gives a brief insight into the symptoms, diagnostics, and treatment of the rare disease Hypophosphatasia (HPP), which is resulting from mutations in the TNAP encoding gene. We emphasize the role of TNAP beyond its well-known contribution to mineralization processes. Therefore, above all, the impact of the enzyme on central molecular processes in the nervous system and on inflammation is presented here.

摘要

这篇综述总结了关于外切酶组织非特异性碱性磷酸酶(TNAP)的重要信息,并简要介绍了由 TNAP 编码基因的突变导致的罕见疾病低磷酸酯酶症(HPP)的症状、诊断和治疗。我们强调了 TNAP 的作用超出了其在矿化过程中的已知贡献。因此,本文主要介绍了该酶对神经系统中中枢分子过程和炎症的影响。

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本文引用的文献

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Innate and Adaptive Immunity in Aging and Longevity: The Foundation of Resilience.衰老与长寿中的先天免疫和适应性免疫:恢复力的基础。
Aging Dis. 2020 Dec 1;11(6):1363-1373. doi: 10.14336/AD.2020.0603. eCollection 2020 Dec.
2
History of ectonucleotidases and their role in purinergic signaling.核苷酸酶的历史及其在嘌呤能信号转导中的作用。
Biochem Pharmacol. 2021 May;187:114322. doi: 10.1016/j.bcp.2020.114322. Epub 2020 Nov 6.
3
Dental defects in the primary dentition associated with hypophosphatasia from biallelic ALPL mutations.
碱性磷酸酶与重度脑白质高信号患者的血管性抑郁有关。
Front Neurosci. 2024 Nov 25;18:1477867. doi: 10.3389/fnins.2024.1477867. eCollection 2024.
4
Bone metabolism in complex regional pain syndrome.复杂性区域疼痛综合征中的骨代谢
Pain Rep. 2024 Nov 20;9(6):e1217. doi: 10.1097/PR9.0000000000001217. eCollection 2024 Dec.
5
Detection of hypophosphatasia in hospitalised adults in rheumatology and internal medicine departments: a multicentre study over 10 years.在风湿科和内科住院成人中检测低磷酸酯酶症:10 年多中心研究。
RMD Open. 2024 Apr 4;10(2):e004316. doi: 10.1136/rmdopen-2024-004316.
6
Serum alkaline phosphatase was independently associated with depression in patients with cerebrovascular disease.血清碱性磷酸酶与脑血管疾病患者的抑郁独立相关。
Front Psychiatry. 2023 Jul 4;14:1184673. doi: 10.3389/fpsyt.2023.1184673. eCollection 2023.
7
TNAP-a potential cytokine in the cerebral inflammation in spastic cerebral palsy.组织非特异性碱性磷酸酶——痉挛型脑瘫脑内炎症中的一种潜在细胞因子
Front Mol Neurosci. 2022 Sep 14;15:926791. doi: 10.3389/fnmol.2022.926791. eCollection 2022.
8
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Pharmaceutics. 2022 Jun 30;14(7):1390. doi: 10.3390/pharmaceutics14071390.
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Biochem Pharmacol. 2021 May;187:114311. doi: 10.1016/j.bcp.2020.114311. Epub 2020 Oct 29.
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Multigenerational case examples of hypophosphatasia: Challenges in genetic counseling and disease management.低磷酸酯酶症的多代病例示例:遗传咨询与疾病管理中的挑战
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