Study finds stem cells in thymus for first time

Stem cells found in the thymus could help researchers better understand immunological disorders, cancer, and ways to stimulate the immune system, according to a new study.
Study finds stem cells in thymus for first time

Washington DC | Researchers have discovered stem cells in the human thymus. These cells represent a potential new target for research into immunological disorders, cancer, and immune system stimulation.

Thymocytes (the gland's cells) grow into T cells, specialised immune cells essential to battling disease, in the thymus, a gland found in the front of the chest. The thymus has a distinct and intricate three-dimensional structure, which includes an epithelium (a layer of cells that can direct T cell development) that wraps around the thymocytes and forms a mesh throughout the entire organ.

As compared to other organs, the thymus has only recently been studied due to its relative difficulty in access, aging-related shrinkage, and recent discovery of its role. It was formerly thought by scientists that it only contained progenitors formed during foetal development, not 'real' epithelial stem cells.

These discoveries, which were just published in Developmental Cell, however, demonstrate for the first time the existence of self-renewing stem cells that give rise to the thymic epithelial cells that guide thymocytes to develop into T cells.

This shows the thymus has a crucial, regenerative function that extends beyond childhood and might be used to strengthen the immune system.

The expression of particular proteins in the human thymus served as the basis for the tests in which the researchers looked at these stem cells. In the thymus, they discovered stem-cell niches (regions where stem cells congregate) in two places, below the organ capsule, or outer layer, and surrounding blood vessels in the medulla, the interior region.

They showed that thymic stem cells contribute to the environment by making extracellular matrix proteins, which serve as their own skeleton.

They discovered that these stem cells, called Polykeratin cells, express a multitude of genes that enable them to give rise to various cell types not previously thought to have a common origin by employing cutting-edge tools to analyse gene expression in single cells and tissue sections.

They have the capacity to differentiate into epithelial, muscular, and neuroendocrine cells, emphasising the role. The scientists were able to demonstrate that thymus stem cells can be greatly enlarged by isolating Polykeratin stem cells in a dish. They showed that a single stem cell could create all the complicated cells in the thymus epithelium, showing a remarkable and unrealized regeneration potential.

Roberta Ragazzini, postdoctoral research associate at the Crick and UCL, and first author, said, “It’s paradoxical that stem cells in the thymus – an organ which reduces in size as we get older – regenerate just as much as those in the skin – an organ which replaces itself every three weeks. The fact that the stem cells give rise to so many different cell types hints at more fundamental functions of the thymus into adulthood.”

It is known that the thymus' activity is closely controlled in adults, giving the immune system just enough boost to combat infections without going beyond and targeting the body's own cells.

However, in some people, the thymus isn't functioning properly or their immune system isn't as strong as it should be. According to the findings of today, it would be advantageous in certain situations to encourage the stem cells to reconstruct the thymus and strengthen their immune system.

Paola Bonfanti, senior group leader of the Epithelial Stem Cell Biology and Regenerative Medicine Laboratory at the Crick, said, “This research is a pivotal shift in our understanding of why we have a thymus capable of regeneration. There are so many important implications of stimulating the thymus to produce more T cells, like helping the immune system respond to vaccinations in the elderly or improving the immune response to cancer.”

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