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Stem cell-based growth, regeneration, and remodeling of the planarian intestine.

Developmental biology | 2011

Although some animals are capable of regenerating organs, the mechanisms by which this is achieved are poorly understood. In planarians, pluripotent somatic stem cells called neoblasts supply new cells for growth, replenish tissues in response to cellular turnover, and regenerate tissues after injury. For most tissues and organs, however, the spatiotemporal dynamics of stem cell differentiation and the fate of tissue that existed prior to injury have not been characterized systematically. Utilizing in vivo imaging and bromodeoxyuridine pulse-chase experiments, we have analyzed growth and regeneration of the planarian intestine, the organ responsible for digestion and nutrient distribution. During growth, we observe that new gut branches are added along the entire anteroposterior axis. We find that new enterocytes differentiate throughout the intestine rather than in specific growth zones, suggesting that branching morphogenesis is achieved primarily by remodeling of differentiated intestinal tissues. During regeneration, we also demonstrate a previously unappreciated degree of intestinal remodeling, in which pre-existing posterior gut tissue contributes extensively to the newly formed anterior gut, and vice versa. By contrast to growing animals, differentiation of new intestinal cells occurs at preferential locations, including within newly generated tissue (the blastema), and along pre-existing intestinal branches undergoing remodeling. Our results indicate that growth and regeneration of the planarian intestine are achieved by co-ordinated differentiation of stem cells and the remodeling of pre-existing tissues. Elucidation of the mechanisms by which these processes are integrated will be critical for understanding organogenesis in a post-embryonic context.

Pubmed ID: 21664348 RIS Download

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Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: F32 DK077469
  • Agency: NIDDK NIH HHS, United States
    Id: F32 DK077469-03
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD043403-07
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD043403
  • Agency: NICHD NIH HHS, United States
    Id: R01-HD043403
  • Agency: Howard Hughes Medical Institute, United States

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