Nature Communications · 2013 · 88 citations · 48 references
Life SciencesDevelopmental BiologyImmunologyInnate ImmunityRegenerative MedicineSignal TransductionComplement SystemComplement-mediated InjuryGrowth Factor SignalingOcular InflammationOcular MorphogenesisRetinal DevelopmentAnaphylatoxin-mediated InflammationComplete RegenerationFibroblast Growth Factor Receptor SignalingGrowth FactorsProgenitor CellsRetinal Progenitor CellsStat3 SignalingTissue Regeneration
Identifying the initiation signals for tissue regeneration in vertebrates is one of the major challenges in regenerative biology. Much of the research thus far has indicated that certain growth factors have key roles. Here we show that complement fragment C3a is sufficient to induce complete regeneration of the embryonic chick retina from stem/progenitor cells present in the eye, independent of fibroblast growth factor receptor signaling. Instead, C3a induces retina regeneration via STAT3 activation, which in turn activates the injury- and inflammation-responsive factors, IL-6, IL-8 and TNF-α. This activation sets forth regulation of Wnt2b, Six3 and Sox2, genes associated with retina stem and progenitor cells. Thus, our results establish a mechanism for retina regeneration based on injury and inflammation signals. Furthermore, our results indicate a unique function for complement anaphylatoxins that implicate these molecules in the induction and complete regeneration of the retina, opening new avenues of experimentation in the field. Components of the complement system have been shown to promote liver regeneration. Haynes et al. demonstrate that the complement fragment C3a can induce regeneration of the embryonic chick retina from stem and progenitor cells of the ciliary margin via activation of STAT3 and other downstream signalling pathways.
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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
PubMed · 1997 · 66.6K citations