Cell study sheds light on damage caused by aging

Scientists have shed light on how the harm caused by senescence -- a vital cell process that plays a key role in diseases of ageing -- could be controlled or even stopped.

Researchers say the findings could have relevance for age-related diseases including cancers and diabetes, although they caution that further research is needed.

During senescence, cells stop dividing. This can be beneficial in assisting wound-healing and preventing excessive growth seen in cancers.

Some aspects of senescence are also harmful and can lead to tissue damage and the deterioration of cell health as seen in diseases of older age.

Scientists at the Medical Research Council's Human Genetics Unit and the Cancer Research UK Edinburgh Centre at the University of Edinburgh focused on a chain of harmful processes triggered by senescence, known as the senescence-associated secretory phenotype (SASP).

The SASP is a cascade of chemical signals that can promote damage to cells through inflammation.

The researchers showed that manipulating a cell's nuclear pores- gateways through which molecules enter the heart of the cell -- prevented triggering of the SASP.

Findings also show that DNA had to be reorganised in space within in the cell's nucleus in order for the SASP to be triggered.

Researchers say the study sheds light on the fundamental workings of the cell and could be instrumental in understanding cell ageing.

The study, published in Genes and Development, was funded by the Medical Research Council and by Cancer Research UK.

Professor Wendy Bickmore, Director of the Human Genetics Unit at the University of Edinburgh's Medical Research Council Institute of Genetics and Molecular Medicine, who led the study, said: "These findings provide us with a much clearer understanding of how senescence causes cell damage. Whilst we are some way from being able to halt the damage caused by the ageing process, we hope that this advance will open up avenues to explore how we might slow some of the harm that stems from senescence. This could be of relevance to the many conditions that tend to affect us as we grow older."

Dr Lindsay Wilson, Programme Manager for Genetics, Epigenetics and Genomics at the Medical Research Council, added: "This study is important because it provides valuable insights in how cells respond to damage and stress. Senescence is an essential self-defence mechanism but at times, can also be harmful. Professor Bickmore's work suggests ways in which scientists of the future might target these harmful effects, for example in age-related diseases."