Angiogenesis precedes myogenesis during regeneration following biopsy injury of skeletal muscle.

IF 5.3 2区 医学 Q2 CELL BIOLOGY Skeletal Muscle Pub Date : 2023-02-14 DOI:10.1186/s13395-023-00313-3
Nicole L Jacobsen, Aaron B Morton, Steven S Segal
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引用次数: 4

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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骨骼肌活检损伤后再生过程中血管生成先于肌肉生成。
背景:急性骨骼肌损伤损伤肌纤维和碎片毛细血管,损害收缩功能和局部灌注。肌纤维和微血管分别从卫星细胞和幸存的微血管碎片中再生,以恢复完整的肌肉。已建立的损伤模型使用肌肉毒素和物理创伤来证明再生过程中肌肉生成和血管生成的同时发生。在这些模型中,efferocytosis去除细胞碎片,而基底层在肌纤维和微血管再生过程中继续提供指导。当肌肉组织被完全移除,局部引导信号丢失时,肌纤维和微血管再生之间的时空耦合是否仍然存在尚不清楚。方法:为了检验完全去除骨骼肌组织是否会影响再生过程中肌肉生成和血管生成之间的时空关系,在成年小鼠臀大肌(GM)中心用活检穿孔(直径2 mm)造成阈下体积肌肉损失。通过伤后21天(dpi)评估空隙再生情况。在活体成像时,通过向循环中注射荧光葡聚糖来评估体内微血管灌注。全贴装GM制剂和组织横截面的共聚焦成像和组织学分析评估了微血管和肌纤维在伤口中的生长情况。结果:填充PDGFRα+和CD45+细胞的临时基质在1 dpi内跨越伤口。再生微血管以7 dpi的速度从创面边缘向基质推进。新生微血管网络在10 dpi时形成,血液灌注网络在14 dpi时跨越伤口。与之形成鲜明对比的是,在7和10 dpi时,伤口仍然没有肌纤维。14 dpi时肌生成进入创面,21 dpi时肌生成穿过创面。与未损伤肌肉相比,再生肌纤维和微血管组织紊乱。结论:在成人骨骼肌穿孔活检后,再生微血管跨越伤口,并在肌纤维再生之前灌注血液。完全组织切除导致的残留引导信号的丢失破坏了微血管和肌纤维再生之间的时空对应关系。我们得出结论,在阈下体积肌肉损失后的再生过程中,血管生成先于肌肉生成。
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来源期刊
Skeletal Muscle
Skeletal Muscle CELL BIOLOGY-
CiteScore
9.10
自引率
0.00%
发文量
25
审稿时长
12 weeks
期刊介绍: The only open access journal in its field, Skeletal Muscle publishes novel, cutting-edge research and technological advancements that investigate the molecular mechanisms underlying the biology of skeletal muscle. Reflecting the breadth of research in this area, the journal welcomes manuscripts about the development, metabolism, the regulation of mass and function, aging, degeneration, dystrophy and regeneration of skeletal muscle, with an emphasis on understanding adult skeletal muscle, its maintenance, and its interactions with non-muscle cell types and regulatory modulators. Main areas of interest include: -differentiation of skeletal muscle- atrophy and hypertrophy of skeletal muscle- aging of skeletal muscle- regeneration and degeneration of skeletal muscle- biology of satellite and satellite-like cells- dystrophic degeneration of skeletal muscle- energy and glucose homeostasis in skeletal muscle- non-dystrophic genetic diseases of skeletal muscle, such as Spinal Muscular Atrophy and myopathies- maintenance of neuromuscular junctions- roles of ryanodine receptors and calcium signaling in skeletal muscle- roles of nuclear receptors in skeletal muscle- roles of GPCRs and GPCR signaling in skeletal muscle- other relevant aspects of skeletal muscle biology. In addition, articles on translational clinical studies that address molecular and cellular mechanisms of skeletal muscle will be published. Case reports are also encouraged for submission. Skeletal Muscle reflects the breadth of research on skeletal muscle and bridges gaps between diverse areas of science for example cardiac cell biology and neurobiology, which share common features with respect to cell differentiation, excitatory membranes, cell-cell communication, and maintenance. Suitable articles are model and mechanism-driven, and apply statistical principles where appropriate; purely descriptive studies are of lesser interest.
期刊最新文献
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