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Updated: Apr 14, 2026

Temporal Quantification of MAPK Induced Expression in Single Yeast Cells
Published on: October 4, 2013
Analysis of exosome release as a cellular response to MAPK pathway inhibition
K Agarwal1, M Saji1, S M Lazaroff1
1William G. Lowrie Department of Chemical and Biomolecular Engineering, Department of Chemistry, Nanoscale Science and Engineering Center for Affordable Nanoenginering of Polymeric Biomedical Devices, Department of Internal Medicine, Division of Endocrinology Diabetes and Metabolism, Arthur G. James Comprehensive Cancer Center and Richard G. Solove Research Institute, The Ohio State University, Columbus, Ohio 43210, United States.
Abstract:
Exosome size distributions and numbers of exosomes released per cell are measured by asymmetric flow-field flow fractionation/multi-angle light scattering (A4F/MALS) for three thyroid cancer cell lines as a function of a treatment that inhibits MAPK signaling pathways in the cells. We show that these cell lines release exosomes with well-defined morphological features and size distributions that reflect a common biological process for their formation and release into the extracellular environment. We find that those cell lines with constitutive activation of the MAPK signaling pathway display MEK-dependent exosome release characterized by increased numbers of exosomes released per cell. Analysis of the measured exosome size distributions based on a generalized extreme value distribution model for exosome formation in intracellular multivesicular bodies highlights the importance of this experimental observable for delineating different mechanisms of vesicle formation and predicting how changes in exosome release can be modified by pathway inhibitors in a cell context-dependent manner.
Insights
Thyroid cancer cells release exosomes with distinct sizes. MAPK pathway inhibition affects exosome release numbers, offering insights into cancer cell communication and therapeutic targets.
Area of Science:
- Cell Biology
- Biochemistry
- Oncology
Background:
- Exosomes are crucial for intercellular communication.
- The MAPK signaling pathway plays a role in cancer progression.
- Understanding exosome release mechanisms is vital for cancer research.
Purpose of the Study:
- To investigate the impact of MAPK signaling inhibition on exosome release in thyroid cancer cells.
- To characterize exosome size distributions and release numbers.
- To explore the relationship between MAPK pathway activation and exosome biogenesis.
Main Methods:
- Asymmetric flow-field flow fractionation/multi-angle light scattering (A4F/MALS) was used to measure exosome size and number.
- Three thyroid cancer cell lines were utilized.
- MAPK signaling pathways were inhibited using specific treatments.
Main Results:
- Thyroid cancer cell lines release exosomes with consistent size distributions.
- Inhibition of MAPK signaling, particularly MEK-dependent pathways, increased exosome release per cell.
- Exosome size distribution analysis provided insights into vesicle formation mechanisms.
Conclusions:
- MAPK signaling pathway activation influences exosome release quantity in thyroid cancer.
- Exosome release is a context-dependent process affected by pathway inhibitors.
- Exosome size distribution analysis is a valuable tool for understanding vesicle formation and predicting therapeutic responses.
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