Researchers from the Rogel Cancer Center and the College of Engineering at the University of Michigan
Proof of Concept for Sample Researchblood of five patients with non-small cell lung cancer demonstrated that the new approach allows the capture of natural killer cells on a microfluidic chip and use them to "grow" NK exosomes.
Exosomes are small sacs of proteins andother molecules that are naturally secreted by almost all types of cells in the body. In this case, we wanted to expand our understanding of NK exosomes and try to use their potential for killing cancer.
Yoon-Tae Kang, Ph.D., co-author of the study
Compared to NK cells, NK exosomes are more stable and easier to modify for therapeutic purposes. The study notes that the system can also aid in the diagnosis and monitoring of cancer.
One of the problems with NK cells is that afterinjections, they do not penetrate into the microenvironment of the tumor. Exosomes derived from NK cells contain the same cancer-killing molecules, but they are much smaller and better penetrate tumors.
While a small number of previousWhile research examined their ability to kill cancer cells, there was no systematic approach to capturing patient-derived NK cells and using them to create exosomes. Another advantage of them is that they are organic, natural for the human body.
Two large natural immune killer cellssurrounded by their much smaller exosomes on the NK-GO microfluidic chip developed at the University of Michigan. Credit: Image Courtesy of Yun-Tae Kang and Zeki Nu
The collection system combines three technologies.The researchers first captured NK cells on a graphene oxide microfluidic chip. The cells are then incubated, prompting them to release the exosomes. They are captured by tiny magnetic beads that are coated with specific antibodies. The beads are then removed from the chip and the NK exosomes are separated from them using a different process.
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