Stem Cell Research & Therapy (Feb 2022)

Epimorphic regeneration of the mouse digit tip is finite

  • Connor P. Dolan,
  • Tae-Jung Yang,
  • Katherine Zimmel,
  • Felisha Imholt,
  • Osama Qureshi,
  • Alyssa Falck,
  • Joshua Gregory,
  • Macie Mayes,
  • Kayla Ritchie,
  • Hannah Koester,
  • Benjamin Daniel,
  • Mingquan Yan,
  • Ling Yu,
  • Larry J. Suva,
  • Dana Gaddy,
  • Lindsay A. Dawson,
  • Ken Muneoka,
  • Regina Brunauer

DOI
https://doi.org/10.1186/s13287-022-02741-2
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 12

Abstract

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Abstract Background Structural regeneration of amputated appendages by blastema-mediated, epimorphic regeneration is a process whose mechanisms are beginning to be employed for inducing regeneration. While epimorphic regeneration is classically studied in non-amniote vertebrates such as salamanders, mammals also possess a limited ability for epimorphic regeneration, best exemplified by the regeneration of the distal mouse digit tip. A fundamental, but still unresolved question is whether epimorphic regeneration and blastema formation is exhaustible, similar to the finite limits of stem-cell mediated tissue regeneration. Methods In this study, distal mouse digits were amputated, allowed to regenerate and then repeatedly amputated. To quantify the extent and patterning of the regenerated digit, the digit bone as the most prominent regenerating element in the mouse digit was followed by in vivo µCT. Results Analyses revealed that digit regeneration is indeed progressively attenuated, beginning after the second regeneration cycle, but that the pattern is faithfully restored until the end of the fourth regeneration cycle. Surprisingly, when unamputated digits in the vicinity of repeatedly amputated digits were themselves amputated, these new amputations also exhibited a similarly attenuated regeneration response, suggesting a systemic component to the amputation injury response. Conclusions In sum, these data suggest that epimorphic regeneration in mammals is finite and due to the exhaustion of the proliferation and differentiation capacity of the blastema cell source.

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