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Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee.淀粉样变命名 2018:国际淀粉样变学会(ISA)命名委员会的建议。
Amyloid. 2018 Dec;25(4):215-219. doi: 10.1080/13506129.2018.1549825. Epub 2019 Jan 7.
3
Systemic amyloidoses and proteomics: The state of the art.系统性淀粉样变性与蛋白质组学:现状
EuPA Open Proteom. 2016 Feb 23;11:4-10. doi: 10.1016/j.euprot.2016.02.003. eCollection 2016 Jun.
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The neXtProt peptide uniqueness checker: a tool for the proteomics community.NextProt 肽独特性检查器:蛋白质组学社区的工具。
Bioinformatics. 2017 Nov 1;33(21):3471-3472. doi: 10.1093/bioinformatics/btx318.
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Implementation and evaluation of amyloidosis subtyping by laser-capture microdissection and tandem mass spectrometry.通过激光捕获显微切割和串联质谱法进行淀粉样变性亚型分型的实施与评估
Clin Proteomics. 2016 Oct 27;13:30. doi: 10.1186/s12014-016-9133-x. eCollection 2016.
6
A comparison of immunohistochemistry and mass spectrometry for determining the amyloid fibril protein from formalin-fixed biopsy tissue.免疫组织化学与质谱分析法在从福尔马林固定活检组织中确定淀粉样原纤维蛋白方面的比较。
J Clin Pathol. 2015 Apr;68(4):314-7. doi: 10.1136/jclinpath-2014-202722. Epub 2015 Jan 30.
7
Nomenclature 2014: Amyloid fibril proteins and clinical classification of the amyloidosis.2014年命名法:淀粉样纤维蛋白与淀粉样变性的临床分类
Amyloid. 2014 Dec;21(4):221-4. doi: 10.3109/13506129.2014.964858. Epub 2014 Sep 29.
8
In vitro amyloidogenic peptides of galectin-7: possible mechanism of amyloidogenesis of primary localized cutaneous amyloidosis.半乳糖凝集素-7的体外淀粉样生成肽:原发性局限性皮肤淀粉样变的淀粉样生成可能机制。
J Biol Chem. 2014 Oct 17;289(42):29195-207. doi: 10.1074/jbc.M114.592998. Epub 2014 Aug 29.
9
Structural mechanism of serum amyloid A-mediated inflammatory amyloidosis.血清淀粉样蛋白 A 介导的炎症性淀粉样变性的结构机制。
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10
How to diagnose amyloidosis.如何诊断淀粉样变性。
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蛋白质组学分析表明,皮下局限性皮肤淀粉样变的主要成分不是半乳糖凝集素-7。

Proteomic analysis shows that the main constituent of subepidermal localised cutaneous amyloidosis is not galectin-7.

机构信息

Hematopathology Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Amyloid. 2021 Mar;28(1):35-41. doi: 10.1080/13506129.2020.1811962. Epub 2020 Sep 1.

DOI:10.1080/13506129.2020.1811962
PMID:32867548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962860/
Abstract

Lichen or macular localised cutaneous amyloidoses have long been described as keratinic amyloidoses and believed to be due to the deposition of cytokeratin peptides originating from epidermis in the dermal papillae. However, recently it was suggested that galectin-7 is the causative protein for this type of amyloidosis. This was based on the detection of galectin-7 in a biopsy from a patient diagnosed with Bowen's disease and localised cutaneous amyloidosis. In this study we report mass spectrometry-based proteomic analysis of the protein composition of localised cutaneous amyloid deposits from seven patients using laser microdissection and show that basal keratins are the main constituents of the amyloid deposits. Galectin-7 was not present in the dermal amyloid deposits and was only present in the overlying Congo red negative epidermis.

摘要

长期以来,人们一直将苔藓样或斑状局限性皮肤淀粉样变描述为角质淀粉样变,并认为其是由于表皮来源的细胞角蛋白肽在真皮乳头沉积所致。然而,最近有研究表明半乳糖凝集素-7 是这种淀粉样变性的致病蛋白。这一观点基于对一位被诊断为 Bowen 病和局限性皮肤淀粉样变患者的活检中发现半乳糖凝集素-7 而提出。在本研究中,我们采用激光显微切割,对 7 位局限性皮肤淀粉样变患者的皮损进行基于质谱的蛋白质组学分析,并显示基底角蛋白是淀粉样沉积物的主要成分。半乳糖凝集素-7 不存在于真皮淀粉样沉积物中,而仅存在于刚果红阴性的表皮上层。

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