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活细胞中表达 INF2 变体时内质网完整性和细胞器相互作用的改变。

Altered Endoplasmic Reticulum Integrity and Organelle Interactions in Living Cells Expressing INF2 Variants.

机构信息

Second Department of Internal Medicine, Division of Nephrology, Kansai Medical University, Hirakata 573-1010, Japan.

Department of Molecular Genetics, Institute of Biochemical Science, Kansai Medical University, Hirakata 573-1010, Japan.

出版信息

Int J Mol Sci. 2024 Sep 10;25(18):9783. doi: 10.3390/ijms25189783.

Abstract

The cytoskeleton mediates fundamental cellular processes by organizing inter-organelle interactions. Pathogenic variants of inverted formin 2 (INF2) CAAX isoform, an actin assembly factor that is predominantly expressed in the endoplasmic reticulum (ER), are linked to focal segmental glomerulosclerosis (FSGS) and Charcot-Marie-Tooth (CMT) neuropathy. To investigate how pathogenic INF2 variants alter ER integrity, we used high-resolution live imaging of HeLa cells. Cells expressing wild-type (WT) INF2 showed a predominant tubular ER with perinuclear clustering. Cells expressing INF2 FSGS variants that cause mild and intermediate disease induced more sheet-like ER, a pattern similar to that seen for cells expressing WT-INF2 that were treated with actin and microtubule (MT) inhibitors. Dual CMT-FSGS INF2 variants led to more severe ER dysmorphism, with a diffuse, fragmented ER and coarse INF2 aggregates. Proper organization of both F-actin and MT was needed to modulate the tubule vs. sheet conformation balance, while MT arrays regulated spatial expansion of tubular ER in the cell periphery. Pathogenic INF2 variants also induced mitochondria fragmentation and dysregulated mitochondria distribution. Such mitochondrial abnormalities were more prominent for cells expressing CMT-FSGS compared to those with FSGS variants, indicating that the severity of the dysfunction is linked to the degree of cytoskeletal disorganization. Our observations suggest that pathogenic INF2 variants disrupt ER continuity by altering interactions between the ER and the cytoskeleton that in turn impairs inter-organelle communication, especially at ER-mitochondria contact sites. ER continuity defects may be a common disease mechanism involved in both peripheral neuropathy and glomerulopathy.

摘要

细胞骨架通过组织细胞器间的相互作用来介导基本的细胞过程。反向formin 2 (INF2) CAAX 同种型的致病变体,一种主要在内质网 (ER) 中表达的肌动蛋白组装因子,与局灶性节段性肾小球硬化症 (FSGS) 和 Charcot-Marie-Tooth (CMT) 神经病有关。为了研究致病性 INF2 变体如何改变 ER 完整性,我们使用了 HeLa 细胞的高分辨率活细胞成像。表达野生型 (WT) INF2 的细胞表现出以核周聚集为主的管状 ER。导致轻度和中度疾病的 INF2 FSGS 变体表达的细胞诱导更多片状 ER,这种模式类似于用肌动蛋白和微管 (MT) 抑制剂处理的表达 WT-INF2 的细胞。双 CMT-FSGS INF2 变体导致更严重的 ER 畸形,表现为弥散、碎片状 ER 和粗糙的 INF2 聚集。适当组织 F-肌动蛋白和 MT 对于调节管 vs. 片状构象平衡是必要的,而 MT 阵列调节细胞外周管状 ER 的空间扩展。致病性 INF2 变体还诱导线粒体碎片化和线粒体分布失调。与 FSGS 变体相比,表达 CMT-FSGS 的细胞中这种线粒体异常更为明显,表明功能障碍的严重程度与细胞骨架解聚的程度有关。我们的观察表明,致病性 INF2 变体通过改变 ER 与细胞骨架之间的相互作用来破坏 ER 的连续性,进而损害细胞器间的通讯,尤其是在 ER-线粒体接触部位。ER 连续性缺陷可能是参与周围神经病和肾小球病的共同疾病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557c/11431639/430fc1c8ca40/ijms-25-09783-g001.jpg

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