New, rapid and robust method for single cell profiling

Many of the cell types in our bodies work in obscure ways that science does not yet fully understand. That also goes for immune cells, which are vital for protecting us against serious diseases.

In order to conquer this obstacle, researchers put a lot of effort into finding new ways to study the inner workings of individual cells.

“The challenge is not only to isolate an individual cell from a tissue sample. We also need to find a way to determine the function of the individual cell,” says Kedar Nath Natarajan, Assistant Professor and Principal Investigator at Department of Biochemistry and Molecular Biology, University of Southern Denmark.

In a new study, led by Kedar Nath Natarajan and Xi Chen from Wellcome Sanger Institute, a research team has developed a new method for microscopically profiling tiny single cells within organs and tissues.

The new method allowed them to analyse more than 3000 cells from the spleen, which is a hot spot for all kinds of immune cells—cells that fight infections, but also render daily immunity and response.

New methods are constantly being developed to microscopically profile tiny single cells within organs and tissues. The principle is to study the basic blueprint of an organism, i.e. DNA and how it is packaged within a single cell. This packaging is referred to as chromatin and signals which genes within the blueprint are switched on and off, thus determining whether it becomes a blood cell, a skin cell, an immune cell, a cancer cell or another type of cell.

“Our new method profiles chromatin within single cells and offers a robust, scalable and cheaper alternative to current state-of-art methods, which require expensive infrastructure, specialized reagents and equipments,” said Kedar Nath Natarajan.

Together with first author Xi Chen from Wellcome Sanger Institute, he has lead the development of the new methods and profile different kinds of cells including immune cells, stem cells etc. The other contributors from Wellcome Sanger Institute are Ricardo J Miragaia and this work was performed in the lab of the corresponding author Sarah A Teichmann.

The paper’s abstract gives this description:

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