Stage Hannah J, Trappe Susanne, Söllig Katharina, Trachsel Dagmar S, Kirsch Katharina, Zieger Cornelia, Merle Roswitha, Aschenbach Jörg R, Gehlen Heidrun
Equine Clinic, Surgery and Radiology, Department of Veterinary Medicine, Freie Universität Berlin, Oertzenweg 19b, 14163 Berlin, Germany.
Institute of Veterinary Physiology, Freie Universität Berlin, Oertzenweg 19b, 14163 Berlin, Germany.
Animals (Basel). 2023 Apr 15;13(8):1352. doi: 10.3390/ani13081352.
The investigation of multipotent stem/stromal cells (MSCs) in vitro represents an important basis for translational studies in large animal models. The study's aim was to examine and compare clinically relevant in vitro properties of equine MSCs, which were isolated from abdominal (abd), retrobulbar (rb) and subcutaneous (sc) adipose tissue by collagenase digestion (ASCs-) and an explant technique (ASCs-). Firstly, we examined proliferation and trilineage differentiation and, secondly, the cardiomyogenic differentiation potential using activin A, bone morphogenetic protein-4 and Dickkopf-1. Fibroblast-like, plastic-adherent ASCs- and ASCs- were obtained from all sources. The proliferation and chondrogenic differentiation potential did not differ significantly between the isolation methods and localizations. However, abd-ASCs- showed the highest adipogenic differentiation potential compared to rb- and sc-ASCs- on day 7 and abd-ASCs- a higher adipogenic potential compared to abd-ASCs- on day 14. Osteogenic differentiation potential was comparable at day 14, but by day 21, abd-ASCs- demonstrated a higher osteogenic potential compared to abd-ASCs- and rb-ASCs-. Cardiomyogenic differentiation could not be achieved. This study provides insight into the proliferation and multilineage differentiation potential of equine ASCs and is expected to provide a basis for future preclinical and clinical studies in horses.
对多能干细胞/基质细胞(MSCs)进行体外研究是大型动物模型转化研究的重要基础。本研究的目的是检测和比较马源MSCs的临床相关体外特性,这些细胞通过胶原酶消化法(ASCs-)和组织块培养法(ASCs-)从腹部(abd)、球后(rb)和皮下(sc)脂肪组织中分离得到。首先,我们检测了细胞的增殖和三系分化能力,其次,使用激活素A、骨形态发生蛋白-4和Dickkopf-1检测了细胞的心肌分化潜能。从所有来源均获得了成纤维细胞样、贴壁生长的ASCs-和ASCs-。两种分离方法和不同部位来源的细胞在增殖和软骨分化潜能方面无显著差异。然而,在第7天,abd-ASCs-与rb-和sc-ASCs-相比,具有最高的成脂分化潜能;在第14天,abd-ASCs-比abd-ASCs-具有更高的成脂潜能。在第14天,成骨分化潜能相当,但到第21天,abd-ASCs-比abd-ASCs-和rb-ASCs-表现出更高的成骨潜能。未实现心肌分化。本研究深入了解了马源ASCs的增殖和多系分化潜能,有望为未来马的临床前和临床研究提供基础。