Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO, USA.
Dalton Cardiovascular Research Center, Columbia, MO, USA.
Skelet Muscle. 2023 Feb 14;13(1):3. doi: 10.1186/s13395-023-00313-3.
Acute injury to skeletal muscle damages myofibers and fragment capillaries, impairing contractile function and local perfusion. Myofibers and microvessels regenerate from satellite cells and from surviving microvessel fragments, respectively, to restore intact muscle. Established models of injury have used myotoxins and physical trauma to demonstrate the concurrence of myogenesis and angiogenesis during regeneration. In these models, efferocytosis removes cellular debris while basal laminae persist to provide guidance during myofiber and microvessel regeneration. It is unknown whether the spatiotemporal coupling between myofiber and microvascular regeneration persists when muscle tissue is completely removed and local guidance cues are lost.
To test whether complete removal of skeletal muscle tissue affects the spatiotemporal relationship between myogenesis and angiogenesis during regeneration, subthreshold volumetric muscle loss was created with a biopsy punch (diameter, 2 mm) through the center of the gluteus maximus (GM) in adult mice. Regeneration into the void was evaluated through 21 days post-injury (dpi). Microvascular perfusion was evaluated in vivo by injecting fluorescent dextran into the circulation during intravital imaging. Confocal imaging and histological analyses of whole-mount GM preparations and tissue cross-sections assessed the growth of microvessels and myofibers into the wound.
A provisional matrix filled with PDGFRα and CD45 cells spanned the wound within 1 dpi. Regenerating microvessels advanced from the edges of the wound into the matrix by 7 dpi. Nascent microvascular networks formed by 10 dpi with blood-perfused networks spanning the wound by 14 dpi. In striking contrast, the wound remained devoid of myofibers at 7 and 10 dpi. Myogenesis into the wound was apparent by 14 dpi and traversed the wound by 21 dpi. Regenerated myofibers and microvessels were disorganized compared to the uninjured muscle.
Following punch biopsy of adult skeletal muscle, regenerating microvessels span the wound and become perfused with blood prior to myofiber regeneration. The loss of residual guidance cues with complete tissue removal disrupts the spatiotemporal correspondence between microvascular and myofiber regeneration. We conclude that angiogenesis precedes myogenesis during regeneration following subthreshold volumetric muscle loss.
骨骼肌的急性损伤会破坏肌纤维和毛细血管片段,从而损害收缩功能和局部灌注。肌纤维和微血管分别由卫星细胞和存活的微血管片段再生,以恢复完整的肌肉。已建立的损伤模型使用肌毒素和物理创伤来证明在再生过程中肌发生和血管生成的同时发生。在这些模型中,噬细胞作用清除细胞碎片,而基膜则保持存在,为肌纤维和微血管再生提供指导。当完全去除肌肉组织并且失去局部导向线索时,肌纤维和微血管再生之间的时空偶联是否持续尚不清楚。
为了测试骨骼肌组织的完全去除是否会影响再生过程中肌发生和血管生成之间的时空关系,通过在成年小鼠的臀大肌(GM)中心使用活检冲孔(直径 2mm)创建亚阈值体积肌肉损失。通过损伤后 21 天(dpi)评估再生情况。通过活体成像过程中将荧光葡聚糖注入循环来评估微血管灌注。通过对整个 GM 准备和组织切片的共聚焦成像和组织学分析评估微血管和肌纤维进入伤口的生长情况。
在 1dpi 时,一个充满 PDGFRα 和 CD45 细胞的临时基质跨越了伤口。在 7dpi 时,再生的微血管从伤口边缘向基质推进。在 10dpi 时形成了新生的微血管网络,在 14dpi 时具有充满血液的网络跨越了伤口。与此形成鲜明对比的是,在 7dpi 和 10dpi 时,伤口仍然没有肌纤维。在 14dpi 时可以看到肌纤维进入伤口,在 21dpi 时穿过伤口。与未受伤的肌肉相比,再生的肌纤维和微血管排列紊乱。
在对成年骨骼肌进行活检冲孔后,再生的微血管跨越伤口并在肌纤维再生之前充满血液。完全去除组织会破坏剩余的导向线索,从而破坏微血管和肌纤维再生之间的时空对应关系。我们得出结论,在亚阈值体积肌肉损失后再生过程中,血管生成先于肌发生。