Blastema formation and periosteal ossification in the regenerating adult mouse digit.

While mammals cannot regenerate amputated limbs, mice and humans have regenerative ability restricted to amputations transecting the digit tip, including the terminal phalanx (P3). In mice, the regeneration process is epimorphic and mediated by the formation of a blastema comprised of undifferentiat...

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Publicado en:Wound Repair & Regeneration Vol. 26; no. 3; pp. 263 - 274
Autores principales: Dawson, Lindsay A., Schanes, Paula P., Kim, Patrick, Imholt, Felisha M., Qureshi, Osama, Dolan, Connor P., Yu, Ling, Yan, Mingquan, Zimmel, Katherine N., Falck, Alyssa R., Muneoka, Ken
Formato: diagnostic images pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell May/Jun2018
Acceso en línea:Ver este registro en EBSCOhost
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        atl: Blastema formation and periosteal ossification in the regenerating adult mouse digit.
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        au:
          Dawson, Lindsay A.
          Schanes, Paula P.
          Kim, Patrick
          Imholt, Felisha M.
          Qureshi, Osama
          Dolan, Connor P.
          Yu, Ling
          Yan, Mingquan
          Zimmel, Katherine N.
          Falck, Alyssa R.
          Muneoka, Ken
        affil: Department of Cell and Molecular Biology, Tulane University, New Orleans Louisiana
      sug:
        subj:
          Osteogenesis
          Bone Regeneration
          Periosteum Physiology
          Animal Studies
          Mice
          Cell Proliferation
          Cell Differentiation
      ab: While mammals cannot regenerate amputated limbs, mice and humans have regenerative ability restricted to amputations transecting the digit tip, including the terminal phalanx (P3). In mice, the regeneration process is epimorphic and mediated by the formation of a blastema comprised of undifferentiated proliferating cells that differentiate to regenerate the amputated structures. Blastema formation distinguishes the regenerative response from a scar‐forming healing response. The mouse digit tip serves as a preclinical model to investigate mammalian blastema formation and endogenous regenerative capabilities. We report that P3 blastema formation initiates prior to epidermal closure and concurrent with the bone histolytic response. In this early healing response, proliferation and cells entering the early stages of osteogenesis are localized to the periosteal and endosteal bone compartments. After the completion of stump bone histolysis, epidermal closure is completed and cells associated with the periosteal and endosteal compartments blend to form the blastema proper. Osteogenesis associated with the periosteum occurs as a polarized progressive wave of new bone formation that extends from the amputated stump and restores skeletal length. Bone patterning is restored along the proximal–distal and medial digit axes, but is imperfect in the dorsal–ventral axis with the regeneration of excessive new bone that accounts for the enhanced regenerated bone volume noted in previous studies. Periosteum depletion studies show that this compartment is required for the regeneration of new bone distal to the original amputation plane. These studies provide evidence that blastema formation initiates early in the healing response and that the periosteum is an essential tissue for successful epimorphic regeneration in mammals.
      pubtype: Academic Journal
      doctype:
        diagnostic images
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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