Differential mitochondrial bioenergetics and cellular resilience in astrocytes, hepatocytes, and fibroblasts from aging baboons

• Published in: GeroScience 2024-04, Vol.46 (5), p.4443-4459
• Main Authors: Adekunbi, Daniel A., Huber, Hillary F., Li, Cun, Nathanielsz, Peter W., Cox, Laura A., Salmon, Adam B.
• Format: Article
• Language: English
• Subjects: Aging; Aging - metabolism; Aging - physiology; Animals; Astrocytes; Astrocytes - metabolism; Bioenergetics; Biomedical and Life Sciences; Cell Biology; Cell proliferation; Cell surface; Cells, Cultured; Energy Metabolism - physiology; Female; Fibroblasts; Fibroblasts - metabolism; Geriatrics/Gerontology; Hepatocytes; Hepatocytes - metabolism; Homeostasis; Hydrogen peroxide; Life Sciences; Male; Mitochondria - metabolism; Molecular Medicine; Neuroimaging; Original; Original Article; Oxidative stress; Oxygen consumption; Papio; Prefrontal cortex; Skin tests; Surface markers; Thapsigargin; Ventricle
• ISSN: 2509-2723; 2509-2715; 2509-2723
• DOI: 10.1007/s11357-024-01155-7

Biological resilience, broadly defined as the ability to recover from an acute challenge and return to homeostasis, is of growing importance to the biology of aging. At the cellular level, there is variability across tissue types in resilience and these differences are likely to contribute to tissue aging rate disparities. However, there are challenges in addressing these cell-type differences at regional, tissue, and subject level. To address this question, we established primary cells from aged male and female baboons between 13.3 and 17.8 years spanning across different tissues, tissue regions, and cell types including (1) fibroblasts from skin and from the heart separated into the left ventricle (LV), right ventricle (RV), left atrium (LA), and right atrium (RA); (2) astrocytes from the prefrontal cortex and hippocampus; and (3) hepatocytes. Primary cells were characterized by their cell surface markers and their cellular respiration was assessed with Seahorse XFe96. Cellular resilience was assessed by modifying a live-cell imaging approach; we previously reported that monitors proliferation of dividing cells following response and recovery to oxidative (50 µM-H 2 O 2 ), metabolic (1 mM-glucose), and proteostasis (0.1 µM-thapsigargin) stress. We noted significant differences even among similar cell types that are dependent on tissue source and the diversity in cellular response is stressor-specific. For example, astrocytes had a higher oxygen consumption rate and exhibited greater resilience to oxidative stress (OS) than both fibroblasts and hepatocytes. RV and RA fibroblasts were less resilient to OS compared with LV and LA, respectively. Skin fibroblasts were less impacted by proteostasis stress compared to astrocytes and cardiac fibroblasts. Future studies will test the functional relationship of these outcomes to the age and developmental status of donors as potential predictive markers.