Related Experiment Video
Updated: Dec 19, 2025

Molecular Modulation by Lentivirus-Delivered Specific shRNAs in Endoplasmic Reticulum Stressed Neurons
Published on: April 24, 2021
Endoplasmic reticulum stress mediated apoptosis via JNK in MWCNT-exposed in vitro systems: size, surface
Nivedita Chatterjee1, Jinhee Choi1
1School of Environmental Engineering, University of Seoul, Korea.
Abstract:
The aim of the present study was to evaluate the underlying mechanism of multi-walled carbon nanotubes (MWCNT) induced cellular response and their potential cross-talk, specifically, between endoplasmic reticulum (ER) stress, MAPK activation and apoptosis and how these nano-bio interactions depend on the physico-chemical properties of MWCNT. For this purpose, human bronchial epithelial (Beas2B) and human hepatoma (HepG2) cell lines, were exposed to five kinds of MWCNTs which differ in functionalization and aspect ratios. Tissue-specific sensitivity was evident for calcium homeostasis, ER-stress response, MAPK activation and apoptosis, which further depended on surface functionalization as well as aspect ratios of MWCNT. By applying specific pharmaceutical inhibitors, relevant biomarkers gene and proteins expressions, we found that possibly MWCNT induce activation of IRE1α-XPB1 pathway-mediated ER-stress response, which in turn trigger apoptosis through JNK activation in both type of cells but with variable intensity. The information presented here would have relevance in better understanding of MWCNT toxicity and their safer applications.
Insights
Multi-walled carbon nanotubes (MWCNTs) trigger cell death by activating endoplasmic reticulum (ER) stress and MAPK pathways. These nano-bio interactions depend on MWCNT properties, influencing toxicity and safe application.
Area of Science:
- Nanotechnology
- Cellular Biology
- Toxicology
Background:
- Multi-walled carbon nanotubes (MWCNTs) are increasingly used, necessitating an understanding of their biological impact.
- Cellular responses to nanomaterials involve complex pathways, including stress responses and apoptosis.
- The physico-chemical properties of MWCNTs can significantly influence their nano-bio interactions.
Purpose of the Study:
- To elucidate the mechanism of MWCNT-induced cellular responses.
- To investigate the cross-talk between endoplasmic reticulum (ER) stress, MAPK activation, and apoptosis.
- To determine the dependence of these nano-bio interactions on MWCNT physico-chemical properties.
Main Methods:
- Exposure of human bronchial epithelial (Beas2B) and hepatoma (HepG2) cell lines to five types of MWCNTs with varying functionalization and aspect ratios.
- Assessment of tissue-specific sensitivity, calcium homeostasis, ER-stress response, MAPK activation, and apoptosis.
- Utilized pharmaceutical inhibitors and analyzed gene and protein expression of relevant biomarkers.
Main Results:
- Tissue-specific sensitivity to MWCNTs was observed, influenced by surface functionalization and aspect ratios.
- MWCNTs induced ER-stress response via the IRE1α-XPB1 pathway.
- ER stress subsequently triggered apoptosis through JNK activation in both cell types, with variable intensity.
Conclusions:
- MWCNT toxicity mechanisms involve ER stress and MAPK pathway activation.
- The physico-chemical properties of MWCNTs dictate the nature and intensity of cellular responses.
- Findings contribute to understanding MWCNT toxicity and promoting safer applications.
More Related Videos
19:44Enhancement of Apoptotic and Autophagic Induction by a Novel Synthetic C-1 Analogue of 7-deoxypancratistatin in Human Breast Adenocarcinoma and Neuroblastoma Cells with Tamoxifen
Published on: May 30, 2012
07:42Activation of Apoptosis by Cytoplasmic Microinjection of Cytochrome c
Published on: June 29, 2011
Related Concept Videos
Regulation of the Unfolded Protein Response
MAPK Signaling Cascades
The Intrinsic Apoptotic Pathway
The Extrinsic Apoptotic Pathway
Apoptosis
The Unfolded Protein Response