Koch Thomas G, Heerkens Tammy, Thomsen Preben D, Betts Dean H
Department of Biomedical Sciences, University of Guelph, Guelph, ON, Canada.
BMC Biotechnol. 2007 May 30;7:26. doi: 10.1186/1472-6750-7-26.
There are no published studies on stem cells from equine cord blood although commercial storage of equine cord blood for future autologous stem cell transplantations is available. Mesenchymal stem cells (MSC) have been isolated from fresh umbilical cord blood of humans collected non-invasively at the time of birth and from sheep cord blood collected invasively by a surgical intrauterine approach. Mesenchymal stem cells isolation percentage from frozen-thawed human cord blood is low and the future isolation percentage of MSCs from cryopreserved equine cord blood is therefore expectedly low. The hypothesis of this study was that equine MSCs could be isolated from fresh whole equine cord blood.
Cord blood was collected from 7 foals immediately after foaling. The mononuclear cell fraction was isolated by Ficoll density centrifugation and cultured in a DMEM low glucose based media at 38.5 degrees C in humidified atmosphere containing 5% CO2. In 4 out of 7 samples colonies with MSC morphology were observed. Cellular morphology varied between monolayers of elongated spindle-shaped cells to layered cell clusters of cuboidal cells with shorter cytoplasmic extensions. Positive Alizarin Red and von Kossa staining as well as significant calcium deposition and alkaline phosphatase activity confirmed osteogenesis. Histology and positive Safranin O staining of matrix glycosaminoglycans illustrated chondrogenesis. Oil Red O staining of lipid droplets confirmed adipogenesis.
We here report, for the first time, the isolation of mesenchymal-like stem cells from fresh equine cord blood and their differentiation into osteocytes, chondrocytes and adipocytes. This novel isolation of equine cord blood MSCs and their preliminary in vitro differentiation positions the horse as the ideal pre-clinical animal model for proof-of-principle studies of cord blood derived MSCs.
尽管已有用于未来自体干细胞移植的马脐带血商业储存服务,但尚无关于马脐带血干细胞的已发表研究。间充质干细胞(MSC)已从人类出生时无创采集的新鲜脐带血以及通过手术子宫内侵入性方法采集的绵羊脐带血中分离出来。从冻融的人类脐带血中分离间充质干细胞的百分比很低,因此预计从冷冻保存的马脐带血中分离间充质干细胞的未来百分比也会很低。本研究的假设是可以从新鲜的全马脐带血中分离出马间充质干细胞。
在7只马驹出生后立即采集脐带血。通过Ficoll密度离心分离单核细胞部分,并在基于低糖DMEM的培养基中于38.5摄氏度、含5%二氧化碳的湿润气氛中培养。在7个样本中的4个中观察到了具有间充质干细胞形态的集落。细胞形态从细长梭形细胞的单层到具有较短细胞质延伸的立方形细胞的分层细胞簇各不相同。茜素红和冯·科萨染色阳性以及显著的钙沉积和碱性磷酸酶活性证实了成骨作用。基质糖胺聚糖的组织学和番红O染色阳性说明了软骨形成。脂滴的油红O染色证实了脂肪形成。
我们首次在此报告从新鲜马脐带血中分离出间充质样干细胞,并将其分化为骨细胞、软骨细胞和脂肪细胞。这种从马脐带血中分离间充质干细胞及其初步体外分化的新方法使马成为脐带血来源间充质干细胞原理验证研究的理想临床前动物模型。