Abstract
Aging is associated with functional and structural declines in many body systems, even in the absence of underlying disease. In particular, skeletal muscles experience severe declines during aging, a phenomenon termed sarcopenia. Despite the high incidence and severity of sarcopenia, little is known about contributing factors and development. Many studies focus on functional aspects of aging-related tissue decline, while structural details remain understudied. Traditional approaches for quantifying structural changes have assessed individual markers at discrete intervals. Such approaches are inadequate for the complex changes associated with aging. An alternative is to consider changes in overall morphology rather than in specific markers. We have used this approach to quantitatively track tissue architecture during adulthood and aging in the C. elegans pharynx, the neuromuscular feeding organ. Using pattern recognition to analyze aged-grouped pharynx images, we identified discrete step-wise transitions between distinct morphologies. The morphology state transitions were maintained in mutants with pharynx neurotransmission defects, although the pace of the transitions was altered. Longitudinal measurements of pharynx function identified a predictive relationship between mid-life pharynx morphology and function at later ages. These studies demonstrate for the first time that adult tissues undergo distinct structural transitions reflecting postdevelopmental events. The processes that underlie these architectural changes may contribute to increased disease risk during aging, and may be targets for factors that alter the aging rate. This work further demonstrates that pattern analysis of an image series offers a novel and generally accessible approach for quantifying morphological changes and identifying structural biomarkers.
Highlights
During development, tissues are built from newly synthesized components along synchronized morphogenic pathways
Longitudinal analysis identifies structural states correlated with future aging success An important issue for understanding the biology of aging is defining whether changes associated with early aging can correlate reliably to future aging success. We addressed this question for the C. elegans pharynx by searching for longitudinal correlations between mid-life morphology and future functional decline
Current thinking holds that tissue structural decline may result from mitochondrial dysfunction, wear and tear, or reduced regenerative capacity at older age [15]
Summary
Tissues are built from newly synthesized components along synchronized morphogenic pathways. During aging, these tissues may deteriorate and exhibit functional declines. Aging-related structural and functional declines are evidence in striated muscles, where loss of muscle mass and strength is referred to as sarcopenia. To identify genes and pathways that maintain tissue structure and function in old age, new approaches for quantifying tissue morphology are needed. Such methodologies would be useful for determining the extent to which adult tissues are structurally static or dynamic
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