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PLK2-mediated phosphorylation of SQSTM1 S349 promotes aggregation of polyubiquitinated proteins upon proteasomal dysfunction 蛋白酶体功能失调时,PLK2 介导的 SQSTM1 S349 磷酸化会促进多泛素化蛋白质的聚集
IF 13.3 1区 生物学 Q1 CELL BIOLOGY Pub Date : 2024-06-19 DOI: 10.1080/15548627.2024.2361574
Yun-Da Chen, Xiu-Ping Lin, Zi-Lun Ruan, Mi Li, Xue-Mei Yi, Xu Zhang, Shu Li, Hong-Bing Shu
Dysregulation in protein homeostasis results in accumulation of protein aggregates, which are sequestered into dedicated insoluble compartments so-called inclusion bodies or aggresomes, where they ...
蛋白质平衡失调会导致蛋白质聚集体的积累,这些聚集体被封存在所谓的包涵体或凝集体(aggresomes)等专用的不溶性区室中,并在其中...
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引用次数: 0
TIGAR exacerbates obesity by triggering LRRK2-mediated defects in macroautophagy and chaperone-mediated autophagy in adipocytes TIGAR 通过引发 LRRK2- 介导的脂肪细胞大自噬和伴侣介导的自噬缺陷,加剧肥胖症的发生
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-30 DOI: 10.1080/15548627.2024.2338576
Tian Zhang, Ke-Gang Linghu, Jia Tan, Mingming Wang, Diao Chen, Yan Shen, Junchao Wu, Mingjun Shi, Yuxia Zhou, Lei Tang, Lirong Liu, Zheng-Hong Qin, Bing Guo
Obesity is one of the most common metabolic diseases around the world, which is distinguished by the abnormal buildup of triglycerides within adipose cells. Recent research has revealed that autoph...
肥胖症是全球最常见的代谢性疾病之一,其特征是甘油三酯在脂肪细胞内异常堆积。最近的研究发现,自噬...
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引用次数: 0
The Wolfram-like variant WFS1E864K destabilizes MAM and compromises autophagy and mitophagy in human and mice 沃尔夫拉姆样变体 WFS1E864K 会破坏 MAM 的稳定性,并损害人类和小鼠的自噬和有丝分裂能力
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-23 DOI: 10.1080/15548627.2024.2341588
Simone Patergnani, Méghane S. Bataillard, Alberto Danese, Stacy Alves, Chantal Cazevieille, René Valéro, Lisbeth Tranebjærg, Tangui Maurice, Paolo Pinton, Benjamin Delprat, Elodie M. Richard
Dominant variants in WFS1 (wolframin ER transmembrane glycoprotein), the gene coding for a mitochondria-associated endoplasmic reticulum (ER) membrane (MAM) resident protein, have been associated w...
WFS1(wolframin ER跨膜糖蛋白)是一种线粒体相关内质网(ER)膜(MAM)驻留蛋白的编码基因,其显性变异与线粒体相关内质网(ER)膜(MAM)驻留蛋白有关。
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引用次数: 0
Autophagy cooperates with PDGFRA to support oncogenic growth signaling 自噬与 PDGFRA 合作支持致癌生长信号转导
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-18 DOI: 10.1080/15548627.2024.2338572
Joanne E. Simpson, Noor Gammoh
Macroautophagy (referred to as autophagy hereafter) is a highly conserved catabolic process which sequesters intracellular substrates for lysosomal degradation. Autophagy-related proteins have been...
大自噬(以下简称自噬)是一种高度保守的分解代谢过程,它将细胞内的底物封存起来供溶酶体降解。与自噬相关的蛋白质已...
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引用次数: 0
Impaired reprogramming of the autophagy flux in maturing dendritic cells from crohn disease patients with core autophagy gene-related polymorphisms 患有核心自噬基因相关多态性的羊角风病患者成熟树突状细胞的自噬通量重编程功能受损
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-14 DOI: 10.1080/15548627.2024.2338574
Gaëlle Quiniou, Leslie Andromaque, Rémi Duclaux-Loras, Océane Dinet, Ornella Cervantes, Mallorie Verdet, Camille Meunier, Gilles Boschetti, Christophe Viret, Stéphane Nancey, Mathias Faure, Aurore Rozières
Crohn disease (CD) is an inflammatory bowel disease whose pathogenesis involves inappropriate immune responses toward gut microbiota on genetically predisposed backgrounds. Notably, CD is associate...
克罗恩病(Crohn disease,CD)是一种炎症性肠病,其发病机制涉及遗传易感人群对肠道微生物群不适当的免疫反应。值得注意的是,克罗恩病与...
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引用次数: 0
Toxic gain-of-function mechanisms in C9orf72 ALS-FTD neurons drive autophagy and lysosome dysfunction C9orf72 ALS-FTD 神经元的毒性功能增益机制驱动自噬和溶酶体功能障碍
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-14 DOI: 10.1080/15548627.2024.2340415
Jimmy Beckers, Philip Van Damme
Hexanucleotide repeat expansions in the C9orf72 gene are the primary genetic cause for both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), two related neurodegenerative dise...
C9orf72基因的六核苷酸重复扩增是肌萎缩侧索硬化症(ALS)和额颞叶痴呆症(FTD)这两种相关神经退行性疾病的主要遗传原因。
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引用次数: 0
Enteric coronavirus nsp2 is a virulence determinant that recruits NBR1 for autophagic targeting of TBK1 to diminish the innate immune response 肠道冠状病毒 nsp2 是一种毒力决定因子,它能招募 NBR1 以 TBK1 为目标进行自噬,从而削弱先天性免疫反应
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-10 DOI: 10.1080/15548627.2024.2340420
Yajuan Jiao, Pengwei Zhao, Ling-Dong Xu, Jia-Qi Yu, Hou-Li Cai, Chong Zhang, Chao Tong, Yong-Le Yang, Pinglong Xu, Qiming Sun, Ning Chen, Bin Wang, Yao-Wei Huang
Non-structural protein 2 (nsp2) exists in all coronaviruses (CoVs), while its primary function in viral pathogenicity, is largely unclear. One such enteric CoV, porcine epidemic diarrhea virus (PED...
非结构蛋白2(nsp2)存在于所有冠状病毒(CoVs)中,但它在病毒致病性中的主要功能目前还不清楚。猪流行性腹泻病毒(PED...
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引用次数: 0
Transformation of autophagic SQSTM1 droplets to SQSTM1-dependent P-bodies 自噬 SQSTM1 小液滴向依赖 SQSTM1 的 P 小体转化
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-10 DOI: 10.1080/15548627.2024.2340413
Evelina Valionyte, Elizabeth R. Barrow, Chris R. Baxter, Sharon Herath, Shouqing Luo
SQSTM1/p62 droplets play crucial roles in droplets-based macroautophagy/autophagy including selective autophagy and bulk autophagy. We observed that under several stress milieus, SQSTM1 droplets en...
SQSTM1/p62液滴在基于液滴的宏自噬/自噬(包括选择性自噬和大量自噬)中发挥着关键作用。我们观察到,在几种应激环境下,SQSTM1小液滴能...
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引用次数: 0
MITOCHONDRIAL IMPORT STRESS and PINK1-MEDIATED MITOPHAGY: THE ROLE of the PINK1-TOMM-TIMM23 SUPERCOMPLEX 间充质输入压力和 PINK1 介导的间充质:PINK1-TOMM-TIMM23 超级复合物的作用
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-10 DOI: 10.1080/15548627.2024.2340399
Mohamed A. Eldeeb, Armaan Fallahi, Andrea Soumbasis, Andrew N. Bayne, Jean-François Trempe, Edward A. Fon
Mutations in the PINK1 kinase cause Parkinson disease (PD) through physiological processes that are not yet fully elucidated. PINK1 kinase accumulates selectively on damaged mitochondria, where it ...
PINK1 激酶突变通过尚未完全阐明的生理过程导致帕金森病(PD)。PINK1 激酶选择性地聚集在受损的线粒体上,在那里...
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引用次数: 0
Massive ER protein disposal by reticulophagy receptors and selective disposal by TOLLIP 网状吞噬受体大规模处理 ER 蛋白质和 TOLLIP 选择性处理 ER 蛋白质
IF 13.3 1区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-04-10 DOI: 10.1080/15548627.2024.2340417
Yuki Hayashi, Hidenori Ichijo
Proteostasis of the endoplasmic reticulum (ER) is maintained by coordinated action of two major catabolic pathways: proteasome-dependent ER-associated degradation (ERAD) and less characterized lyso...
内质网(ER)的蛋白稳态是通过两种主要分解途径的协调作用来维持的:蛋白酶体依赖的ER相关降解(ERAD)和特征较少的溶酶体降解。
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引用次数: 0
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Autophagy
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