Chen Ning, Kamath Siddharth, Newcomb Jennifer, Hudson Jennifer, Garbuzova-Davis Svitlana, Bickford Paula, Davis-Sanberg Cyndy, Sanberg Paul, Zigova Tanja, Willing Alison
Center of Excellence for Aging & Brain Repair, Department of Neurosurgery, University of South Florida, 12901 Bruce B Downs Blvd, Tampa, FL 33612, USA.
J Neural Eng. 2007 Jun;4(2):130-45. doi: 10.1088/1741-2560/4/2/013. Epub 2007 Apr 4.
The mononuclear fraction of human umbilical cord blood (HUCBmnf) is a mixed cell population that multiple research groups have shown contains cells that can express neural proteins. In these studies, we have examined the ability of the HUCBmnf to express neural antigens after in vitro exposure to defined media supplemented with a cocktail of growth and neurotrophic factors. It is our hypothesis that by treating the HUCBmnf with these developmentally-relevant factors, we can expand the population, enhance the expression of neural antigens and increase cell survival upon transplantation. Prior to growth factor treatment in culture, expression of stem cell antigens is greater in the non-adherent HUCBmnf cells compared to the adherent cells (p < 0.05). Furthermore, treatment of the non-adherent cells with growth factors, increases BrdU incorporation, especially after 14 days in vitro (DIV). In HUCBmnf-embryonic mouse striata co-culture, a small number of growth factor treated HUCBmnf cells were able to integrate into the growing neural network and express immature (nestin and TuJ1) and mature (GFAP and MAP2) neural markers. Treated HUCBmnf cells implanted in the subventricular zone predominantly expressed GFAP although some grafted HUCBmnf cells were MAP2 positive. While short-term treatment of HUCBmnf cells with growth and neurotrophic factors enhanced proliferative capacity in vitro and survival of the cells in vivo, the treatment regimen employed was not enough to ensure long-term survival of HUCBmnf-derived neurons necessary for cell replacement therapies for neurodegenerative diseases.
人脐带血单核细胞部分(HUCBmnf)是一个混合细胞群体,多个研究小组已表明其包含能够表达神经蛋白的细胞。在这些研究中,我们检测了HUCBmnf在体外暴露于添加了生长因子和神经营养因子混合物的特定培养基后表达神经抗原的能力。我们的假设是,通过用这些与发育相关的因子处理HUCBmnf,我们可以扩大细胞群体,增强神经抗原的表达,并提高移植后细胞的存活率。在培养中进行生长因子处理之前,与贴壁细胞相比,非贴壁HUCBmnf细胞中干细胞抗原的表达更高(p < 0.05)。此外,用生长因子处理非贴壁细胞会增加BrdU掺入,尤其是在体外培养14天后(DIV)。在HUCBmnf与胚胎小鼠纹状体的共培养中,少数经生长因子处理的HUCBmnf细胞能够整合到生长的神经网络中,并表达未成熟(巢蛋白和TuJ1)和成熟(GFAP和MAP2)神经标记物。植入脑室下区的经处理HUCBmnf细胞主要表达GFAP,尽管一些移植的HUCBmnf细胞为MAP2阳性。虽然用生长因子和神经营养因子对HUCBmnf细胞进行短期处理可增强其体外增殖能力和体内细胞存活率,但所采用的处理方案不足以确保HUCBmnf衍生神经元的长期存活,而这对于神经退行性疾病的细胞替代疗法是必需的。