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Key Molecule of Aging The Molecule that Controls Our Life Span

Editor: MA Alexander Stark

Scientists at the German Cancer Research Center in Heidelberg have discovered for the first time a protein that represents a central switching point in the aging process. It controls the life span of an individual — from the fly to the human being.

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Scientists at the German Cancer Research Center in Heidelberg have discovered a key molecule of aging.
Scientists at the German Cancer Research Center in Heidelberg have discovered a key molecule of aging.
(Source: Pixabay / CC0 )

Heidelberg/Germany — Oxidative stress causes cells and entire organisms to age. If reactive oxygen species accumulate, this causes damage to the DNA as well as changes in the protein molecules and lipids in the cell. The cell ultimately loses its functionality and dies. Over time, the tissue suffers and the body ages. The theory of oxidative stress or the accumulation of reactive oxygen species as the cause of aging has existed since the 1950s. So far, however, the details of this process were unclear, explains Peter Krammer of the German Cancer Research Center (DKFZ).

In fact, reactive oxygen species do more than just damage the body. For example, they are essential for the T-cells of the immune system to become active. DKFZ researchers led by Krammer and Karsten Gülow* have now discovered the key regulator that is responsible for shifting the sensitive balance from vital to harmful amounts of reactive oxygen molecules and thus accelerating the aging process: A protein molecule called TXNIP (thioredoxin-interacting protein).

Protection Against Oxidative Stress

One way in which the body disposes of harmful reactive oxygen species is their conversion by the enzyme thioredoxin-1 (TRX-1). TRX-1 has been proven to play a role in protecting DNA from oxidative stress and slowing down aging processes. Its antagonist TXNIP inhibits thioredoxin-1 and thus ensures that the reactive oxygen molecules are retained.

The DKFZ researchers led by Krammer and Gülow now wanted to know whether more TXNIP is formed in the body with increasing age, thereby undermining the protective mechanism against oxidative stress. To this end, they first compared T cells from the blood of a group of over 55-year-old volunteers with the T cells of younger blood donors, who were between 20 and 25 years old. In fact, it turned out that the cells of older subjects produce significantly more TXNIP. The DKFZ scientists have also observed similar findings in other human cell and tissue types.

Fly Experiments

The researchers also found out that more TXNIP is produced in the fly Drosophila with increasing age. In order to test whether TXNIP is actually responsible for aging, they bred flies that produce significantly more TXNIP than their relatives as well as flies in which TXNIP synthesis is greatly reduced. According to Tina Oberacker, who was responsible for the fly experiments, flies that produced more TXNIP lived on average much shorter, while flies with less TXNIP had a longer average life.

TRX-1 and its opponent TXNIP are highly conserved in the course of evolution; they hardly differ between flies and humans, the scientists found. It could therefore be assumed that the two proteins perform similar functions in flies and humans. If more TXNIP is produced with increasing age, this means that TRX is gradually switched off with its protection function. This leads to more oxidative stress, which damages cells and tissue and eventually causes them to die.

Krammer is convinced that TXNIP is a key regulator for aging. "Scientists have found hundreds of genes that are somehow related to the aging process," says the DKFZ researcher summarizing the results. But it was enough to switch off TXNIP to delay aging. Similarly, aging can be accelerated if they got the cells to produce TXNIP. And that made it an interesting candidate to intervene in the aging process in the future, Krammer concludes.

The research was funded by the European Union and the Wilhelm Sander Foundation.

Tina Oberacker, Jörg Bajorat, Sabine Ziola, Anne Schroeder, Daniel Röth, Lena Kastl, Bruce A. Edgar, Wolfgang Wagner, Karsten Gülow, Peter H. Krammer: Enhanced expression of thioredoxin interacting protein regulates oxidative DNA damage and aging. FEBS Letters, 2018, doi: 10.1002/1873-3468.13156

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