Laboratory of Muscle Plasticity, Department of Orthopedics, University of Zurich, Balgrist Campus, Zürich, Switzerland.
Musculoskeletal Research Unit, Center for Applied Biotechnology and Molecular Medicine, Department of Molecular Mechanisms, Vetsuisse Faculty, University of Zurich, Zürich, Switzerland.
Am J Sports Med. 2021 Dec;49(14):3970-3980. doi: 10.1177/03635465211052566. Epub 2021 Oct 29.
The injection of mesenchymal stem cells (MSCs) mitigates fat accumulation in released rotator cuff muscle after tendon repair in rodents.
To investigate whether the injection of autologous MSCs halts muscle-to-fat conversion after tendon repair in a large animal model for rotator cuff tendon release via regional effects on extracellular fat tissue and muscle fiber regeneration.
Controlled laboratory study.
Infraspinatus (ISP) muscles of the right shoulder of Swiss Alpine sheep (n = 14) were released by osteotomy and reattached 16 weeks later without (group T; n = 6) or with (group T-MSC; n = 8) electropulse-assisted injection of 0.9 Mio fluorescently labeled MSCs as microtissues with media in demarcated regions; animals were allowed 6 weeks of recovery. ISP volume and composition were documented with computed tomography and magnetic resonance imaging. Area percentages of muscle fiber types, fat, extracellular ground substance, and fluorescence-positive tissue; mean cross-sectional area (MCSA) of muscle fibers; and expression of myogenic (myogenin), regeneration (tenascin-C), and adipogenic markers (peroxisome proliferator-activated receptor gamma [PPARG2]) were quantified in injected and noninjected regions after recovery.
At 16 weeks after tendon release, the ISP volume was reduced and the fat fraction of ISP muscle was increased in group T (137 vs 185 mL; 49% vs 7%) and group T-MSC (130 vs 166 mL; 53% vs 10%). In group T-MSC versus group T, changes during recovery after tendon reattachment were abrogated for fat-free mass (-5% vs -29%, respectively; = .018) and fat fraction (+1% vs +24%, respectively; = .009%). The area percentage of fat was lower (9% vs 20%; = .018) and the percentage of the extracellular ground substance was higher (26% vs 20%; = .007) in the noninjected ISP region for group T-MSC versus group T, respectively. Regionally, MCS injection increased tenascin-C levels (+59%) and the water fraction, maintaining the reduced PPARG2 levels but not the 29% increased fiber MCSA, with media injection.
In a sheep model, injection of autologous MSCs in degenerated rotator cuff muscle halted muscle-to-fat conversion during recovery from tendon repair by preserving fat-free mass in association with extracellular reactions and stopping adjuvant-induced muscle fiber hypertrophy.
A relatively small dose of MSCs is therapeutically effective to halt fatty atrophy in a large animal model.
间质干细胞(MSCs)的注射减轻了啮齿动物修复肌腱后释放的旋转袖肌肉中的脂肪积累。
通过对外周脂肪组织和肌肉纤维再生的区域影响,研究自体 MSC 注射是否能在肩袖肌腱释放的大动物模型中阻止肌腱修复后的肌肉向脂肪转化。
对照实验室研究。
瑞士阿尔卑斯羊(n = 14)右侧冈下肌(ISP)通过截骨术释放,并在 16 周后重新连接,不(组 T;n = 6)或用(组 T-MSC;n = 8)电脉冲辅助注射 0.9 万个荧光标记的 MSC 作为微组织与介质在划定的区域;动物允许恢复 6 周。用计算机断层扫描和磁共振成像记录 ISP 体积和成分。肌肉纤维类型、脂肪、细胞外基质和荧光阳性组织的面积百分比;肌肉纤维的平均横截面积(MCSA);以及注射和非注射区域的成肌(myogenin)、再生(tenascin-C)和脂肪生成标志物(过氧化物酶体增殖物激活受体γ[PPARG2])的表达。
在肌腱释放后 16 周时,组 T(137 对 185 毫升;49%对 7%)和组 T-MSC(130 对 166 毫升;53%对 10%)的 ISP 体积减少,ISP 肌肉的脂肪分数增加。与组 T 相比,组 T-MSC 中的脂肪分数在肌腱再附着后的恢复期间发生变化(+1%对+24%; =.009)。与组 T 相比,非注射 ISP 区域的脂肪百分比更低(9%对 20%; =.018),细胞外基质的百分比更高(26%对 20%; =.007)。区域上,MSC 注射增加了 tenascin-C 水平(+59%)和水分数,保持了降低的 PPARG2 水平,但没有增加纤维 MCSA 的 29%,而介质注射则增加了纤维 MCSA 的 29%。
在绵羊模型中,自体 MSC 注射可阻止肌腱修复后的肌肉向脂肪转化,方法是在与细胞外反应相关的情况下保留无脂肪质量,并阻止辅助诱导的肌肉纤维肥大。
在大型动物模型中,较小剂量的 MSC 治疗是有效的,可阻止脂肪萎缩。