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      Rapid population-wide declines in stem cell number and activity during reproductive aging in C. elegans

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          ABSTRACT

          C. elegans hermaphrodites display dramatic age-related decline of reproduction early in life, while somatic functions are still robust. To understand reproductive aging, we analyzed the assembly line of oocyte production that generates fertilized eggs. Aging germlines displayed both sporadic and population-wide changes. A small fraction of aging animals displayed endomitotic oocytes in the germline and other defects. By contrast, all animals displayed age-related decreases in germline size and function. As early as day 3 of adulthood, animals displayed fewer stem cells and a slower cell cycle, which combine to substantially decrease progenitor zone output. The C. elegans germline is the only adult tissue that contains stem cells, allowing the analysis of stem cells in aging. To investigate the mechanism of the decrease in stem cell number, we analyzed the Notch signaling pathway. The Notch effectors LST-1 and SYGL-1 displayed age-related decreases in expression domains, suggesting a role for Notch signaling in germline aging. The results indicate that although sporadic defects account for the sterility of some animals, population-wide changes account for the overall pattern of reproductive aging.

          Abstract

          [Related article:] Highlighted Article: Age-related reproductive decline in C. elegans results from sporadic defects in some animals, but primarily from population-wide processes affecting stem cell number, Notch signaling, cell cycle timing, and meiotic entry and progression.

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          Author and article information

          Journal
          Development
          Development
          DEV
          develop
          Development (Cambridge, England)
          The Company of Biologists Ltd
          0950-1991
          1477-9129
          15 April 2019
          23 April 2019
          15 April 2020
          : 146
          : 8
          : dev173195
          Affiliations
          [1 ] Department of Developmental Biology, Washington University School of Medicine , St Louis, MO 63110, USA
          [2 ] Department of Genetics, Washington University School of Medicine , St Louis, MO 63110, USA
          Author notes
          [*]

          These authors contributed equally to this work

          []Author for correspondence ( ts@ 123456wustl.edu )
          Author information
          http://orcid.org/0000-0002-8573-1376
          http://orcid.org/0000-0002-6042-5241
          http://orcid.org/0000-0003-2148-2996
          Article
          PMC6503983 PMC6503983 6503983 DEV173195
          10.1242/dev.173195
          6503983
          30936182
          8e19975a-3968-44d3-a313-39f6f3408d8f
          © 2019. Published by The Company of Biologists Ltd
          History
          : 30 October 2018
          : 13 March 2019
          Funding
          Funded by: National Institutes of Health, http://dx.doi.org/10.13039/100000002;
          Award ID: R01 GM100756
          Funded by: National Institutes of Health, http://dx.doi.org/10.13039/100000002;
          Award ID: R01 AG02656106A1
          Funded by: National Science Foundation, http://dx.doi.org/10.13039/100000001;
          Award ID: DGE-1143954
          Award ID: DGE-1745038
          Funded by: The Douglas Covey Fellowship;
          Categories
          203
          208
          Stem Cells and Regeneration

          Germline,Endomitotic oocytes,Cell cycle,Reproductive aging,Meiotic development,Notch,Stem cells, Caenorhabditis

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