Study of impacts of two types of cellular aging on the yeast bud morphogenesis
Year: 2024
Type: article
Abstract: Understanding the mechanisms of cellular aging processes is crucial for attempting to extend organismal lifespan and for studying age-related degenerative diseases. Yeast cells divide through budding, providing a classical biological model for studying cellular aging. With their powerful genetics, relatively short lifespan and well-established signaling pathways also found in animals, yeast cells offer valuable insights into the aging process. Recent experiments suggested the existence of two aging modes in yeast characterized by nucleolar and mitochondrial declines, respectively. In this study, by analyzing experimental data it was shown that cells evolving into those two aging modes behave differently when they are young. While buds grow linearly in both modes, cells that consistently generate spherical buds throughout their lifespan demonstrate greater efficacy in controlling bud size and growth rate at young ages. A three-dimensional chemical-mechanical model was developed and used to suggest and test hypothesized mechanisms of bud morphogenesis during aging. Experimentally calibrated simulations showed that tubular bud shape in one aging mode could be generated by locally inserting new materials at the bud tip guided by the polarized Cdc42 signal during the early stage of budding. Furthermore, the aspect ratio of the tubular bud could be stabilized during the late stage, as observed in experiments, through a reduction on the new cell surface material insertion or an expansion of the polarization site. Thus model simulations suggest the maintenance of new cell surface material insertion or chemical signal polarization could be weakened due to cellular aging in yeast and other cell types. Significance Statement Aging yeast exhibits two modes with different bud shapes. Experimental data analysis reveals that control of growth rate and bud size is more robust in cells aging in a spherical budding mode than in cells aging in a tubular budding mode. A computational model was developed and used in combination with experiments to test the hypothesized mechanisms underlying different types of budding in aging cells. Model simulations suggest that localized growth is sufficient to generate tubular budding and its aspect ratio can be stabilized through the regulation of chemical signals with an expanding polarization site or a decline on the new cell surface material insertion. Proposed mechanisms of morphological changes in aging yeast can be present in other cell types.
Source: PLoS Computational Biology
Language: English
Subfield: Aging
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,926
Funders: National Science Foundation, Foundation for the National Institutes of Health, U.S. Department of Energy, University of California, National Institutes of Health, University of California, Riverside, National Institute on Aging, National Institute of General Medical Sciences, Division of Materials Research, Biological and Environmental Research
Awards: Engineered genetic clocks for control of cellular aging, Integrating at Sub-Cellular Level the Biochemical and Biomechanical Signals with Stochasticity to Study the Regulation of Tissue Growth, G1774047169, G1804640201, G1928851605, G2029375272, G2089094767, G2573548193, MODULUS: Integrative multiscale modeling and multimodal experiments to decode systems-level molecular mecanisms of epithelial systems, G2789014146, Research Infrastructure: MRI: Acquisition of a Big Data HPC Cluster for Interdisciplinary Research and Training, G3894772981, CAREER: Multiscale Model for Cell Morphogenesis and Tissue Development in Plant Leaves, Physics of virus assembly and disassembly: Energetics and dynamics, Collaborative Research: eMB: Data-driven mechano-chemical models of morphogenesis on deforming domains, G7196764177, G8238154194, G8399528858, G9000121103, G9000252760, Systems biology analysis of RNA-binding protein aggregation during cellular aging
OpenAlex ID: W4402977972
