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Fundamental differences in dedifferentiation and stem cell recruitment during skeletal muscle regeneration in two salamander species

机译:两种sal骨骼肌再生过程中去分化和干细胞募集的根本差异

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Salamanders regenerate appendages via a progenitor pool called the blastema. The cellular mechanisms underlying regeneration of muscle have been much debated but have remained unclear. Here we applied Cre-loxP genetic fate mapping to skeletal muscle during limb regeneration in two salamander species, Notophthalmus viridescens (newt) and Ambystoma mexicanum (axolotl). Remarkably, we found that myofiber dedifferentiation is an integral part of limb regeneration in the newt, but not in axolotl. In the newt, myofiber fragmentation results in proliferating, PAX7- mononuclear cells in the blastema that give rise to the skeletal muscle in the new limb. In contrast, myofibers in axolotl do not generate proliferating cells, and do not contribute to newly regenerated muscle; instead, resident PAX7+ cells provide the regeneration activity. Our results therefore show significant diversity in limb muscle regeneration mechanisms among salamanders and suggest that multiple strategies may be feasible for inducing regeneration in other species, including mammals.
机译:am通过称为胚母细胞的祖细胞再生附肢。肌肉再生的基础细胞机制已经争论不休,但仍不清楚。在这里,我们在两个sal物种Notophthalmus viridescens(newt)和Ambystoma mexicanum(axolotl)的肢体再生过程中,将Cre-loxP遗传命运图谱应用于骨骼肌。值得注意的是,我们发现肌纤维去分化是the中肢体再生不可或缺的一部分,而不是a。在the中,肌纤维断裂导致胚泡中增殖的PAX7单核细胞增生,形成新肢体的骨骼肌。相反,x中的肌纤维不会产生增殖细胞,也不会促进新再生的肌肉。相反,常驻PAX7 +细胞提供再生活性。因此,我们的研究结果表明sal在肢体肌肉再生机制上存在显着差异,并提出了多种策略来诱导其他物种(包括哺乳动物)的再生可能是可行的。

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