Altamirano Dallas E, Mihaly Eszter, Emmens Jalissa D, Grayson Warren L
Translational Tissue Engineering Center, School of Medicine, Johns Hopkins University, Baltimore, MD, 21231, USA.
Department of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD, 21205, USA.
Adv Biol (Weinh). 2024 Dec;8(12):e2400113. doi: 10.1002/adbi.202400113. Epub 2024 Sep 18.
Tissue-engineered muscle grafts (TEMGs) are a promising treatment for volumetric muscle loss (VML). In this study, human myogenic progenitors (hMPs) cultured on electrospun fibrin microfiber bundles and evaluated the therapeutic potential of engineered hMP TEMGs in the treatment of murine tibialis anterior (TA) VML injuries is employed. In vitro, the hMP TEMGs express mature muscle markers by 21 days. Upon implantation into VML injuries, the hMP TEMGs enable remarkable regeneration. To further promote wound healing and myogenesis, human adipose-derived stem/stromal cells (hASCs) as fibroadipogenic progenitor (FAP)-like cells with the potential to secrete pro-regenerative cytokines are incorporated. The impact of dose and timing of seeding the hASCs on in vitro myogenesis and VML recovery using hMP-hASC TEMGs are investigated. The hASCs increase myogenesis of hMPs when co-cultured at 5% hASCs: 95% hMPs and with delayed seeding. Upon implantation into immunocompromised mice, hMP-hASC TEMGs increase cell survival, collagen IV deposition, and pro-regenerative macrophage recruitment, but result in excessive adipose tissue growth after 28 days. These data demonstrate the interactions of hASCs and hMPs enhance myogenesis in vitro but there remains a need to optimize treatments to minimize adipogenesis and promote full therapeutic recovery following VML treatment.
组织工程肌肉移植物(TEMGs)是治疗大面积肌肉缺损(VML)的一种有前景的方法。在本研究中,使用在电纺纤维蛋白微纤维束上培养的人肌源性祖细胞(hMPs),并评估工程化hMP TEMGs治疗小鼠胫骨前肌(TA)VML损伤的治疗潜力。在体外,hMP TEMGs在21天时表达成熟的肌肉标志物。植入VML损伤部位后,hMP TEMGs能实现显著的再生。为了进一步促进伤口愈合和肌生成,加入了人脂肪来源的干/基质细胞(hASCs),其作为具有分泌促再生细胞因子潜力的纤维脂肪生成祖细胞(FAP)样细胞。研究了接种hASCs的剂量和时间对使用hMP-hASC TEMGs的体外肌生成和VML恢复的影响。当以5% hASCs: 95% hMPs的比例共培养且延迟接种时,hASCs可增加hMPs的肌生成。植入免疫缺陷小鼠后,hMP-hASC TEMGs可提高细胞存活率、增加IV型胶原沉积并促进促再生巨噬细胞募集,但在28天后会导致过多脂肪组织生长。这些数据表明,hASCs与hMPs的相互作用在体外可增强肌生成,但仍需要优化治疗方法,以尽量减少脂肪生成并促进VML治疗后的完全治疗恢复。