Ahern Benjamin J, Schaer Thomas P, Terkhorn Shawn P, Jackson Karen V, Mason Nicola J, Hankenson Kurt D
Department of Clinical Studies-New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA 19348, USA.
Am J Vet Res. 2011 Jan;72(1):127-33. doi: 10.2460/ajvr.72.1.127.
To evaluate effects of apheresis on mesenchymal stem cells (MSCs) and compare those MSCs with MSCs obtained from adipose tissue or bone marrow (BM).
Samples obtained from 6 adult horses.
Samples of blood from a peripheral vein, adipose tissue, and BM aspirate were obtained from each horse. Samples were processed via apheresis of blood and techniques reported elsewhere for adipose tissue and BM. Cultures were maintained until adherence and subsequently were subjected to differentiation protocols to evaluate adipogenic, osteoblastogenic, and chondrogenic potential.
Apheresis product had a significantly higher mononuclear percentage, higher platelet count, and lower RBC count, compared with values for peripheral blood. No cell adherence to the tissue culture plates was detected for the apheresis product. Adherence was detected for 6 of 6 adipose-derived and 4 of 6 BM-derived samples. Variations in efficiency were detected for differentiation of adipose- and BM-derived cells into adipocytes, chondrocytes, and osteoblasts.
Apheresis was able to concentrate mononuclear cells and reduce RBC contamination. However, the apheresis product was unable to adhere to the tissue culture plates. In matched horses, adipose- and BM-derived MSCs were capable of producing lipids, glycosaminoglycan, and mineral. The BM was vastly superior to adipose tissue as a source of MSCs with osteoblastogenic potential in matched horses. Additional studies will be necessary to optimize apheresis techniques for horses before peripheral blood can be considered a suitable source for multipotential cells for use in cell-based treatments.
评估单采术对间充质干细胞(MSC)的影响,并将这些MSC与从脂肪组织或骨髓(BM)获取的MSC进行比较。
从6匹成年马获取的样本。
从每匹马采集外周静脉血、脂肪组织和骨髓抽吸物样本。通过血液单采术以及其他地方报道的脂肪组织和骨髓技术对样本进行处理。培养细胞直至贴壁,随后进行分化方案以评估成脂、成骨和成软骨潜能。
与外周血相比,单采产物的单核细胞百分比显著更高、血小板计数更高且红细胞计数更低。未检测到单采产物的细胞贴附于组织培养板。6个脂肪来源样本中的6个以及6个骨髓来源样本中的4个检测到贴壁。在脂肪来源和骨髓来源的细胞分化为脂肪细胞、软骨细胞和成骨细胞的过程中检测到效率差异。
单采术能够浓缩单核细胞并减少红细胞污染。然而,单采产物无法贴附于组织培养板。在匹配的马匹中,脂肪来源和骨髓来源的MSC能够产生脂质、糖胺聚糖和矿物质。在匹配的马匹中,作为具有成骨潜能的MSC来源,骨髓远远优于脂肪组织。在将外周血视为基于细胞治疗中多能细胞的合适来源之前,有必要进行更多研究以优化马匹的单采技术。