CIRIMAT, Université Toulouse III Paul Sabatier, CNRS UMR 5085, INPT, Faculté de Pharmacie, 35 Chemin des Maraichers, CEDEX 09, 31062 Toulouse, France.
Department of Oral Medicine and Toulouse University Hospital (CHU of Toulouse)-Toulouse Institute of Oral Medicine and Science, CEDEX 09, 31062 Toulouse, France.
Int J Mol Sci. 2023 Jan 22;24(3):2206. doi: 10.3390/ijms24032206.
Adipose-derived mesenchymal stromal cells (ASC) transplant to recover the optimal tissue structure/function relationship is a promising strategy to regenerate tissue lesions. Because filling local tissue defects by injection alone is often challenging, designing adequate cell carriers with suitable characteristics is critical for in situ ASC delivery. The aim of this study was to optimize the generation phase of a platelet-lysate-based fibrin hydrogel (PLFH) as a proper carrier for in situ ASC implantation and (1) to investigate in vitro PLFH biomechanical properties, cell viability, proliferation and migration sustainability, and (2) to comprehensively assess the local in vivo PLFH/ASC safety profile (local tolerance, ASC fate, biodistribution and toxicity). We first defined the experimental conditions to enhance physicochemical properties and microscopic features of PLFH as an adequate ASC vehicle. When ASC were mixed with PLFH, in vitro assays exhibited hydrogel supporting cell migration, viability and proliferation. In vivo local subcutaneous and subgingival PLFH/ASC administration in nude mice allowed us to generate biosafety data, including biodegradability, tolerance, ASC fate and engraftment, and the absence of biodistribution and toxicity to non-target tissues. Our data strongly suggest that this novel combined ATMP for in situ administration is safe with an efficient local ASC engraftment, supporting the further development for human clinical cell therapy.
脂肪来源的间充质基质细胞(ASC)移植以恢复最佳的组织结构/功能关系是再生组织损伤的一种有前途的策略。由于仅通过注射填充局部组织缺陷常常具有挑战性,因此设计具有合适特性的足够细胞载体对于原位 ASC 递呈至关重要。本研究的目的是优化基于血小板裂解物的纤维蛋白水凝胶(PLFH)的生成阶段,将其作为原位 ASC 植入的合适载体,并(1)研究 PLFH 的体外生物力学特性、细胞活力、增殖和迁移可持续性,以及(2)全面评估局部体内 PLFH/ASC 的安全性概况(局部耐受性、ASC 命运、生物分布和毒性)。我们首先确定了实验条件,以增强 PLFH 的物理化学性质和微观特征,将其作为合适的 ASC 载体。当 ASC 与 PLFH 混合时,体外检测显示水凝胶支持细胞迁移、活力和增殖。在裸鼠的局部皮下和龈下 PLFH/ASC 给药的体内研究中,我们获得了生物安全性数据,包括生物降解性、耐受性、ASC 命运和植入,以及非目标组织中无生物分布和毒性。我们的数据强烈表明,这种新型原位给药的联合 ATMP 是安全的,具有有效的局部 ASC 植入,支持进一步开发用于人体临床细胞治疗。