Olguin Hugo C, Yang Zhihong, Tapscott Stephen J, Olwin Bradley B
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
J Cell Biol. 2007 Jun 4;177(5):769-79. doi: 10.1083/jcb.200608122.
Postnatal growth and regeneration of skeletal muscle requires a population of resident myogenic precursors named satellite cells. The transcription factor Pax7 is critical for satellite cell biogenesis and survival and has been also implicated in satellite cell self-renewal; however, the underlying molecular mechanisms remain unclear. Previously, we showed that Pax7 overexpression in adult primary myoblasts down-regulates MyoD and prevents myogenin induction, inhibiting myogenesis. We show that Pax7 prevents muscle differentiation independently of its transcriptional activity, affecting MyoD function. Conversely, myogenin directly affects Pax7 expression and may be critical for Pax7 down-regulation in differentiating cells. Our results provide evidence for a cross-inhibitory interaction between Pax7 and members of the muscle regulatory factor family. This could represent an additional mechanism for the control of satellite cell fate decisions resulting in proliferation, differentiation, and self-renewal, necessary for skeletal muscle maintenance and repair.
骨骼肌的出生后生长和再生需要一群名为卫星细胞的驻留肌源性前体细胞。转录因子Pax7对卫星细胞的生成和存活至关重要,并且也与卫星细胞的自我更新有关;然而,其潜在的分子机制仍不清楚。此前,我们发现成年原代成肌细胞中Pax7的过表达会下调MyoD并阻止肌细胞生成素的诱导,从而抑制肌生成。我们发现Pax7独立于其转录活性阻止肌肉分化,影响MyoD功能。相反,肌细胞生成素直接影响Pax7的表达,并且可能对分化细胞中Pax7的下调至关重要。我们的结果为Pax7与肌肉调节因子家族成员之间的交叉抑制相互作用提供了证据。这可能代表了一种控制卫星细胞命运决定的额外机制,这些决定导致增殖、分化和自我更新,这对骨骼肌的维持和修复是必要的。