Scientists unlock path to use cell’s own nanoparticles as disease biomarkers
Researchers at the University of Sydney have established a method to identify individual nanoparticles released by human cells, opening the way for them to become diagnostic tools in the early-detection of cancers, dementia and kidney disease.
The particles, known as extracellular vesicles, or EVs, are routinely released by cells and play a central role in cell communication, sharing vital information such as DNA, RNA and proteins.
“This really is at the cutting edge of our knowledge of cellular development,” said Associate Professor Wojciech Chrzanowski, co-author of a new paper on EVs published in the Royal Society of Chemistry’s Nanoscale Horizons.
“EVs could not only be used to identify cellular pathologies but because they carry essential information about cell development, we could engineer them for purposes of tissue repair.”
Associate Professor Chrzanowski from the University of Sydney Nano Institute and the Faculty of Pharmacy said the ability to identify individual EVs will provide biomarkers for diverse diseases such as cancers, cardiovascular, kidney and liver disease as well as dementia and multiple sclerosis.
He said it will also allow scientists to engineer EVs for use in tissue regeneration and help start a new chapter in stem-cell therapies and regenerative medicine.
“The human body naturally directs EVs from stem cells to damaged tissue to assist in its repair. By harnessing this knowledge, we could create a new generation of cell therapies,” said Associate Professor Chrzanowski, who is the industry theme leader for Health and Medicine at Sydney Nano.
Understanding the particular nature of EVs is therefore essential for developing their application for diagnostics and therapeutics. For instance, early-stage cancerous cells release EVs that indicate the presence of malignant tissue in the body.
The study of extracellular vesicles is a relatively new field. It is only in the past decade that it has been known that cells communicate and transfer molecular and genetic information using EVs.
The full potential to harness this knowledge for biomedical use has been hampered due to difficulties in establishing the heterogeneous nature of EV populations. Until now, they have only been analysed as large-scale populations with insufficient sensitivity.
Lead author of the paper, doctoral candidate Sally Yunsun Kim, said: “To unlock the true potential of EVs, what is needed is a new approach to unequivocally define nanoscale differences at a single EV level – and that is what we have done.”
This is because it is the individual nature of the EVs as released by cells – affected by cellular morphology, genetics and environment – that give them their agency in human tissue repair.
Ms Kim, Associate Professor Chrzanowski and their team have developed a way to identify individual EV nanostructures, through examination of human placental stem cells provided by co-author Dr Bill Kalionis from the Royal Women’s Hospital in Melbourne.
In the Nanoscale Horizons paper the team details a new method to identify the nanoscale composition of EVs using “resonance-enhanced atomic force microscope infrared spectroscopy” (AFM-IR).
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