Mesenchymal stromal cell aging impairs the self-organizing capacity of lung alveolar epithelial stem cells

D Chanda, M Rehan, SR Smith, KG Dsouza, Y Wang… - Elife, 2021 - elifesciences.org
D Chanda, M Rehan, SR Smith, KG Dsouza, Y Wang, K Bernard, D Kurundkar, V Memula…
Elife, 2021elifesciences.org
Multicellular organisms maintain structure and function of tissues/organs through emergent,
self-organizing behavior. In this report, we demonstrate a critical role for lung mesenchymal
stromal cell (L-MSC) aging in determining the capacity to form three-dimensional organoids
or 'alveolospheres' with type 2 alveolar epithelial cells (AEC2s). In contrast to L-MSCs from
aged mice, young L-MSCs support the efficient formation of alveolospheres when co-
cultured with young or aged AEC2s. Aged L-MSCs demonstrated features of cellular …
Abstract
Multicellular organisms maintain structure and function of tissues/organs through emergent, self-organizing behavior. In this report, we demonstrate a critical role for lung mesenchymal stromal cell (L-MSC) aging in determining the capacity to form three-dimensional organoids or ‘alveolospheres’ with type 2 alveolar epithelial cells (AEC2s). In contrast to L-MSCs from aged mice, young L-MSCs support the efficient formation of alveolospheres when co-cultured with young or aged AEC2s. Aged L-MSCs demonstrated features of cellular senescence, altered bioenergetics, and a senescence-associated secretory profile (SASP). The reactive oxygen species generating enzyme, NADPH oxidase 4 (Nox4), was highly activated in aged L-MSCs and Nox4 downregulation was sufficient to, at least partially, reverse this age-related energy deficit, while restoring the selforganizing capacity of alveolospheres. Together, these data indicate a critical role for cellular bioenergetics and redox homeostasis in an organoid model of self-organization and support the concept of thermodynamic entropy in aging biology.
eLife