Apparently it does matter where a cell ages, as a team of bioinformaticians from the aging research cluster of excellence CECAD at the University of Cologne and the Cologne Max Planck Institute for Biology of Aging have now shown. Using cells in the mouse liver, they examined which role the location of the cell in the organ plays during ageing. The results of the study were published in Nature Aging under the title ‘Spatial and single-cell profiling of the metabolome, transcriptome and epigenome of the aging mouse liver’.
The location of the liver cells has a strong influence on the ageing process. In the region of the liver where the liver cells use oxygen for energy production in their mitochondria, this process deteriorated significantly with increasing age. In the central, oxygen-deprived area of the liver, however, the researchers found no change in the mitochondria, but a change in the cells' fat metabolism.
“It is important where cells age. They age differently depending on where they are located and what their function is,” said Peter Tessarz, research group leader at the Max Planck Institute for Biology of Ageing and leader of the study.“ For ageing research, this means that we have to pay close attention to which cells we are studying and where they are located in the organ.
The liver is largely made up of a single type of cell, the hepatocyte. Depending on where they are located in the liver, they have different roles. Near the portal vein, where fresh, oxygenated blood enters the liver, hepatocytes use the oxygen to process fats in their mitochondria and produce energy. In contrast, carbohydrates are broken down in the less oxygen-rich regions of the liver.
“In the liver, the position of the hepatocyte in the organ plays a crucial role. That's why the liver was the perfect model for us to investigate whether location also makes a difference in ageing,” explains Peter Tessarz.
The researchers analysed liver cells from young and old mice using cutting-edge technology that allowed them not only to obtain data for almost every single cell, but also to assign it to a position in the organ. They were particularly interested in which genes were still being read in old age, how the metabolism of the cells changed and whether epigenetic changes occurred. According to Achim Tresch, head of the Institute for Medical Statistics and Bioinformatics, whose bioinformatics group belongs to the CECAD, the work shows “that the bioinformatic combination of different types of data at the single-cell level produces new insights into metabolic processes.”
Media Contact:
Prof. Achim Tresch
Institute of Medical Statistics and Computational Biology
CECAD – Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases
+49 221 478 96512
achim.tresch@uni-koeln.de
Press and Communications Team:
Susanne Kutter
CECAD Public Relations Officer
+49 221 478-84043
susanne.kutter[at]uni-koeln.de
Press and public relations: Dr. Maren Berghoff
Max Planck Institute for Biology of Ageing, Cologne
Tel.: +49 (0)221 379 70 207
E-mail: maren.berghoff[at]age.mpg.de
Publication:
https://www.nature.com/articles/s43587-023-00513-y
Verantwortlich: Dr. Elisabeth Hoffmann – e.hoffmann@verw.uni-koeln.de