Department of Biology, Miami University, Oxford, Ohio 45056, USA.
Nat Commun. 2013;4:2312. doi: 10.1038/ncomms3312.
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.
鉴定脊椎动物组织再生的起始信号是再生生物学的主要挑战之一。到目前为止,大部分研究表明某些生长因子具有关键作用。在这里,我们发现补体片段 C3a 足以诱导胚胎鸡视网膜从眼睛中存在的干细胞/祖细胞完全再生,而无需成纤维细胞生长因子受体信号。相反,C3a 通过 STAT3 激活诱导视网膜再生,继而激活损伤和炎症反应因子 IL-6、IL-8 和 TNF-α。这种激活规定了与视网膜干细胞和祖细胞相关的 Wnt2b、Six3 和 Sox2 基因的调控。因此,我们的结果建立了一种基于损伤和炎症信号的视网膜再生机制。此外,我们的结果表明补体过敏毒素具有独特的功能,这些分子参与了视网膜的诱导和完全再生,为该领域的实验开辟了新途径。