Induction of the CD24 Surface Antigen in Primary Undifferentiated Human Adipose Progenitor Cells by the Hedgehog Signaling Pathway

F. Muoio, S. Panella, Yves Harder, T. Tallone
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Abstract

In the murine model system of adipogenesis, the CD24 cell surface protein represents a valuable marker to label undifferentiated adipose progenitor cells. Indeed, when injected into the residual fat pads of lipodystrophic mice, these CD24 positive cells reconstitute a normal white adipose tissue (WAT) depot. Unluckily, similar studies in humans are rare and incomplete. This is because it is impossible to obtain large numbers of primary CD24 positive human adipose stem cells (hASCs). This study shows that primary hASCs start to express the glycosylphosphatidylinositol (GPI)-anchored CD24 protein when cultured with a chemically defined medium supplemented with molecules that activate the Hedgehog (Hh) signaling pathway. Therefore, this in vitro system may help understand the biology and role in adipogenesis of the CD24-positive hASCs. The induced cells’ phenotype was studied by flow cytometry, Real-Time Quantitative Polymerase Chain Reaction (RT-qPCR) techniques, and their secretion profile. The results show that CD24 positive cells are early undifferentiated progenitors expressing molecules related to the angiogenic pathway.
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Hedgehog信号通路诱导CD24表面抗原在原代未分化人脂肪祖细胞中的作用
在小鼠脂肪生成模型系统中,CD24细胞表面蛋白是标记未分化脂肪祖细胞的有价值的标志物。事实上,当注射到脂肪营养不良小鼠的残余脂肪垫中时,这些CD24阳性细胞重建了正常的白色脂肪组织(WAT)库。不幸的是,在人类身上进行的类似研究很少而且不完整。这是因为不可能获得大量的原代CD24阳性的人脂肪干细胞(hASCs)。这项研究表明,当与补充有激活Hedgehog(Hh)信号通路分子的化学定义培养基培养时,原代hASCs开始表达糖基磷脂酰肌醇(GPI)锚定的CD24蛋白。因此,该体外系统可能有助于理解CD24阳性hASCs的生物学和在脂肪生成中的作用。通过流式细胞术、实时定量聚合酶链反应(RT-qPCR)技术研究诱导细胞的表型及其分泌谱。结果表明,CD24阳性细胞是表达与血管生成途径相关分子的早期未分化祖细胞。
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