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细胞死亡过程中细胞黏附与核膜纳米拓扑结构的结构与功能分析

Structural and functional analysis of cell adhesion and nuclear envelope nano-topography in cell death.

作者信息

Kwon Hyuk-Kwon, Lee Jae-Hyeok, Shin Hyeon-Jun, Kim Jae-Ho, Choi Sangdun

机构信息

Department of Molecular Science and Technology, Ajou University, Suwon 443-749, Korea.

Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

Sci Rep. 2015 Oct 22;5:15623. doi: 10.1038/srep15623.

Abstract

The cell death mechanisms of necrosis and apoptosis generate biochemical and morphological changes in different manners. However, the changes that occur in cell adhesion and nuclear envelope (NE) topography, during necrosis and apoptosis, are not yet fully understood. Here, we show the different alterations in cell adhesion function, as well as the topographical changes occurring to the NE, during the necrotic and apoptotic cell death process, using the xCELLigence system and atomic force microscopy (AFM). Studies using xCELLigence technology and AFM have shown that necrotic cell death induced the expansion of the cell adhesion area, but did not affect the speed of cell adhesion. Necrotic nuclei showed a round shape and presence of nuclear pore complexes (NPCs). Moreover, we found that the process of necrosis in combination with apoptosis (termed nepoptosis here) resulted in the reduction of the cell adhesion area and cell adhesion speed through the activation of caspases. Our findings showed, for the first time, a successful characterization of NE topography and cell adhesion during necrosis and apoptosis, which may be of importance for the understanding of cell death and might aid the design of future drug delivery methods for anti-cancer therapies.

摘要

坏死和凋亡的细胞死亡机制以不同方式产生生化和形态学变化。然而,在坏死和凋亡过程中细胞黏附及核膜(NE)拓扑结构发生的变化尚未完全明确。在此,我们使用xCELLigence系统和原子力显微镜(AFM)展示了坏死性和凋亡性细胞死亡过程中细胞黏附功能的不同改变以及NE发生的拓扑结构变化。使用xCELLigence技术和AFM的研究表明,坏死性细胞死亡诱导细胞黏附面积扩大,但不影响细胞黏附速度。坏死细胞核呈圆形且存在核孔复合体(NPC)。此外,我们发现坏死与凋亡相结合的过程(此处称为nepoptosis)通过半胱天冬酶的激活导致细胞黏附面积和细胞黏附速度降低。我们的研究结果首次成功表征了坏死和凋亡过程中的NE拓扑结构及细胞黏附情况,这对于理解细胞死亡可能具有重要意义,并且可能有助于设计未来用于抗癌治疗的药物递送方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1021/4614995/b96a7e09835c/srep15623-f1.jpg

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