网状内皮系统中的巨噬细胞抑制小鼠载脂蛋白A-II淀粉样变性的早期诱导阶段。

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hiroki Miyahara, Jian Dai, Ying Li, Xiaoran Cui, Hibiki Takeuchi, Naomi Hachiya, Fuyuki Kametani, Masahide Yazaki, Masayuki Mori, Keiichi Higuchi
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引用次数: 0

摘要

淀粉样变性是指一组变性疾病,其特征是在各个器官中沉积错误折叠的蛋白原纤维。沉积的淀粉样蛋白可以被依赖吞噬细胞的先天免疫系统清除;然而,疾病进展过程中的确切机制尚不清楚。我们在此研究巨噬细胞在淀粉样蛋白降解和疾病进展中的特性,使用诱导性载脂蛋白A-II淀粉样变性模型小鼠。静脉注射的AApoAII淀粉样蛋白被肝脏和脾脏网状内皮巨噬细胞有效吞噬,并在24小时内消失。虽然培养的小鼠巨噬细胞通过内体-溶酶体途径降解AApoAII,但AApoAII原纤维降低了细胞活力和吞噬能力。此外,在AApoAII诱导前,网状内皮巨噬细胞的消耗显著增加了肝脏和脾脏的AApoAII沉积。这些结果强调了网状内皮巨噬细胞在发病早期的生理作用,并建议维持吞噬完整性作为抑制疾病进展的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macrophages in the reticuloendothelial system inhibit early induction stages of mouse apolipoprotein A-II amyloidosis.

Amyloidosis refers to a group of degenerative diseases that are characterized by the deposition of misfolded protein fibrils in various organs. Deposited amyloid may be removed by a phagocyte-dependent innate immune system; however, the precise mechanisms during disease progression remain unclear. We herein investigated the properties of macrophages that contribute to amyloid degradation and disease progression using inducible apolipoprotein A-II amyloidosis model mice. Intravenously injected AApoAII amyloid was efficiently engulfed by reticuloendothelial macrophages in the liver and spleen and disappeared by 24 h. While cultured murine macrophages degraded AApoAII via the endosomal-lysosomal pathway, AApoAII fibrils reduced cell viability and phagocytic capacity. Furthermore, the depletion of reticuloendothelial macrophages before the induction of AApoAII markedly increased hepatic and splenic AApoAII deposition. These results highlight the physiological role of reticuloendothelial macrophages in the early stages of pathogenesis and suggest the maintenance of phagocytic integrity as a therapeutic strategy to inhibit disease progression.

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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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