Physiology Section, Department of Biomedical and Biotechnological Sciences, University of Catania, via S. Sofia, 97, 95123, Catania, Italy.
Division of Hematology, AOU "Policlinico-San Marco", via S. Sofia, 78, 95123, Catania, Italy.
Histochem Cell Biol. 2021 Jul;156(1):35-46. doi: 10.1007/s00418-021-01980-3. Epub 2021 Mar 16.
The influences of ghrelin on neural differentiation of adipose-derived mesenchymal stem cells (ASCs) were investigated in this study. The expression of typical neuronal markers, such as protein gene product 9.5 (PGP9.5) and Microtubule Associated Protein 2 (MAP2), as well as glial Fibrillary Acid Protein (GFAP) as a glial marker was evaluated in ASCs in different conditions. In particular, 2 µM ghrelin was added to control ASCs and to ASCs undergoing neural differentiation. For this purpose, ASCs were cultured in Conditioned Media obtained from Olfactory Ensheathing cells (OEC-CM) or from Schwann cells (SC-CM). Data on marker expression were gathered after 1 and 7 days of culture by fluorescence immunocytochemistry and flow cytometry. Results show that only weak effects were induced by the addition of only ghrelin. Instead, dynamic ghrelin-induced modifications were detected on the increased marker expression elicited by glial conditioned media. In fact, the combination of ghrelin and conditioned media consistently induced a further increase of PGP9.5 and MAP2 expression, especially after 7 days of treatment. The combination of ghrelin with SC-CM produced the most evident effects. Weak or no modifications were found on conditioned medium-induced GFAP increases. Observations on the ghrelin receptor indicate that its expression in control ASCs, virtually unchanged by the addition of only ghrelin, was considerably increased by CM treatment. These increases were enhanced by combining ghrelin and CM treatment, especially at 7 days. Overall, it can be assumed that ghrelin favors a neuronal rather than a glial ASC differentiation.
本研究旨在探讨 ghrelin 对脂肪间充质干细胞(ASCs)神经分化的影响。在不同条件下评估 ASCs 中典型神经元标志物(如蛋白基因产物 9.5(PGP9.5)和微管相关蛋白 2(MAP2))以及神经胶质标志物胶质纤维酸性蛋白(GFAP)的表达。特别是在对照组 ASCs 和进行神经分化的 ASCs 中添加 2μM 的 ghrelin。为此,将 ASCs 培养在嗅鞘细胞(OEC-CM)或施万细胞(SC-CM)产生的条件培养基中。通过荧光免疫细胞化学和流式细胞术在培养 1 天和 7 天后收集标记物表达的数据。结果表明,仅添加 ghrelin 仅引起微弱的影响。相反,在神经胶质条件培养基引起的标记物表达增加的情况下,检测到 ghrelin 诱导的动态修饰。事实上,ghrelin 和条件培养基的组合一致地诱导 PGP9.5 和 MAP2 表达的进一步增加,特别是在 7 天的治疗后。ghrelin 和 SC-CM 的组合产生了最明显的效果。在条件培养基诱导的 GFAP 增加方面,未观察到弱或无修饰。对 ghrelin 受体的观察表明,其在仅添加 ghrelin 时基本不变的对照组 ASCs 中的表达,在 CM 处理后显著增加。这种增加通过 ghrelin 和 CM 处理的组合得到增强,尤其是在 7 天时。总体而言,可以假设 ghrelin 有利于 ASC 向神经元而非神经胶质分化。