Three Distinct Mechanisms Found To Protect Cells From Formaldehyde During Aging

AMeD syndrome is a severe genetic condition found in children that present with accelerated ageing, global developmental delay and bone marrow failure, among others, progressing to Myelodysplastic Syndrome and Acute Myeloid Leukaemia. It is caused by mutations in the ADH5 and ALDH2 genes, which are responsible for the transformation of formaldehyde, a known environmental hazard, into less toxic compounds. In AMeD patients, however, formaldehyde accumulates within the cells and attacks the cellular components, overwhelming the repair machinery.

Formaldehyde is a quite simple yet reactive organic compound that can be found in building materials, household products, cigarette smoke, and vehicle emissions. However, it is more than just an environmental hazard since formaldehyde can also be produced within your cells as a by-product of your own metabolism. Indeed, during normal growth your cells produce this reactive toxin that may cause some trouble if not properly detoxified. The good news is that your cells have a plethora of repair systems built-in that avoid or correct most of the damage caused by formaldehyde.

For a long time, researchers have wondered which of the detoxification and repair systems are the most relevant to counteract formaldehyde toxicity, especially considering it can act over many different cellular components, producing a great diversity of damage, that require largely different repair tools. Nevertheless, finding the right in vivo model have proven difficult up until now.

A recent work led by the teams of Prof. Bjoern Schumacher the University of Cologne, Germany, and of Dr. Lucas Pontel from the Josep Carreras Leukaemia Research Institute, reported the development of a genetically tractable animal model of AMeD. The research, published in the prestigious journal Nucleic Acid Research, used the roundworm C. elegans and patient-derived human cells to resolve which are the key mechanisms that protect the genome from formaldehyde during development, adulthood and ageing.

The researchers identified at least three distinct mechanisms that address formaldehyde-induced DNA damage: 1) in the germline and early embryonic development, the preferred repair mechanism is the Global Genome Nucleotide Excision Repair, a system capable of repairing the DNA at bulk, frequently used to protect cells from UV radiation. 2) In adults and non-dividing cells, where DNA is not being replicated, formaldehyde toxicity is counteracted by the canonical Transcription-Coupled Repair, which normally deals with DNA lesions in coding genes that are actively being transcribed. 3) During development, when cells are dividing, the preferred mechanism is a branch of the Transcription-Coupled Repair system operating independently of the canonical Nucleotide Excision Repair, a system used to resolve DNA-protein crosslinks.

The identification of the key repair mechanisms for formaldehyde-induced damage is a valuable piece of information. However, the team of researchers went beyond and found that the known antioxidant and formaldehyde quencher N-acetyl-L-cysteine (NAC) could reverse most of the toxicity in the animal model of AMeD and in human cells with alterations on the DNA repair systems, offering an unexpected clue for a potential therapeutic intervention to revert formaldehyde-pathogenic consequences.

While this research is still on the preclinical stage, the researchers are confident that it can inspire new therapeutic and dietary interventions to reduce the toxicity of this metabolic toxin, not only for AMeD patients, but also for individuals with familiar history of cancer development.

Reference: Rieckher M, Gallrein C, Alquezar-Artieda N, et al. Distinct DNA repair mechanisms prevent formaldehyde toxicity during development, reproduction and aging. Nucleic Acids Research. 2024;52(14):8271-8285. doi: 10.1093/nar/gkae519

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.