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Single‐cell high‐content imaging parameters predict functional phenotype of cultured human bone marrow stromal stem cells

机译:单细胞高含量成像参数预测培养的人骨髓基质干细胞的功能表型

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Cultured human bone marrow stromal (mesenchymal) stem cells (hBM‐MSCs) are heterogenous cell populations exhibiting variable biological properties. Quantitative high‐content imaging technology allows identification of morphological markers at a single cell resolution that are determinant for cellular functions. We determined the morphological characteristics of cultured primary hBM‐MSCs and examined their predictive value for hBM‐MSC functionality. BM‐MSCs were isolated from 56 donors and characterized for their proliferative and differentiation potential. We correlated these data with cellular and nuclear morphological features determined by Operetta; a high‐content imaging system. Cell area, cell geometry, and nucleus geometry of cultured hBM‐MSCs exhibited significant correlation with expression of hBM‐MSC membrane markers: ALP, CD146, and CD271. Proliferation capacity correlated negatively with cell and nucleus area and positively with cytoskeleton texture features. In addition, in vitro differentiation to osteoblasts as well as in vivo heterotopic bone formation was associated with decreased ratio of nucleus width to length. Multivariable analysis applying a stability selection procedure identified nuclear geometry and texture as predictors for hBM‐MSCs differentiation potential to osteoblasts or adipocytes. Our data demonstrate that by employing a limited number of cell morphological characteristics, it is possible to predict the functional phenotype of cultured hBM‐MSCs and thus can be used as a screening test for “quality” of hBM‐MSCs prior their use in clinical protocols.
机译:培养的人骨髓基质(间充质)干细胞(HBM-MSCs)是表现出可变生物特性的异源细胞群。定量高含量成像技术允许以单细胞分辨率鉴定为细胞功能的决定簇的形态标志物。我们确定了培养的原发性HBM-MSCs的形态特征,并检查了HBM-MSC功能的预测值。 BM-MSCs分离出56个供体,其特征在于它们的增殖和分化潜力。我们将这些数据与由Operetta确定的细胞和核形态特征相关联;高含量的成像系统。培养的HBM-MSCs的细胞面积,细胞几何形状和核几何形状表现出与HBM-MSC膜标记的表达显着相关:ALP,CD146和CD271。扩散能力与细胞和核区域产生负面相关,呈呈细胞骨架纹理特征。此外,对成骨细胞的体外分化以及体内异位骨形成与细胞核宽度与长度的降低相关。应用稳定性选择程序的多变量分析将核几何形状和纹理作为骨质细胞或脂肪细胞的HBM-MSCs分化电位的预测因子。我们的数据表明,通过采用有限数量的细胞形态特征,可以预测培养的HBM-MSC的功能表型,因此可以用作HBM-MSCs的“质量”的筛选试验,在临床方案中使用。

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