Lang Changhui, Shu Xiaomei, Peng Longying, Yu Xiaohua
Department of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi, 563003, Guizhou, China.
Cytotechnology. 2019 Oct;71(5):977-988. doi: 10.1007/s10616-019-00339-w. Epub 2019 Sep 5.
Central nervous system diseases remain the most challenging pathologies, with limited or even no therapeutic possibilities and a poor prognosis. This study aimed to investigate the differentiation properties of human umbilical cord blood mesenchymal stem cells (hUCB-MSCs) transfected with recombinant adenovirus expressing enhanced green fluorescence protein cardiotrophin-1 (Adv-EGFP-CT-1) and the possible mechanisms involved. Cells were isolated, and MSC immunophenotypes were confirmed. The resulting differentiated cells treated with Adv-EGFP-CT-1 and cultured in neural induction medium (NIM) expressed higher levels of Nestin, neuronal nuclei (NeuN) and glial fibrillary acidic protein (GFAP) markers than cells in other treatments. Expression of glycoprotein 130/leukemia inhibitory factor receptor β (gp130/LiFRβ), Raf-1, phosphorylated Raf-1 (p-Raf-1), extracellular signal-regulated kinase 1/2 (ERK1/2) and phospho-ERK1/2 (p-ERK1/2) increased gradually within 72 h after transfection with Adv-EGFP-CT-1 and NIM culture. Additionally, inhibition of extracellular signal-regulated kinase kinase (MEK) abrogated expression of p-ERK1/2, Nestin, GFAP and NeuN. Thus, the ERK1/2 pathway may contribute to CT1-stimulated neural differentiation of hUCB-MSCs.
中枢神经系统疾病仍然是最具挑战性的病理学问题,治疗可能性有限甚至没有,预后也很差。本研究旨在探讨转染表达增强型绿色荧光蛋白心肌营养素-1的重组腺病毒(Adv-EGFP-CT-1)的人脐带血间充质干细胞(hUCB-MSCs)的分化特性及其可能涉及的机制。分离细胞并确认MSC免疫表型。用Adv-EGFP-CT-1处理并在神经诱导培养基(NIM)中培养的所得分化细胞比其他处理中的细胞表达更高水平的巢蛋白、神经元细胞核(NeuN)和胶质纤维酸性蛋白(GFAP)标志物。糖蛋白130/白血病抑制因子受体β(gp130/LiFRβ)、Raf-1、磷酸化Raf-1(p-Raf-1)、细胞外信号调节激酶1/2(ERK1/2)和磷酸化ERK1/2(p-ERK1/2)的表达在转染Adv-EGFP-CT-1并进行NIM培养后72小时内逐渐增加。此外,抑制细胞外信号调节激酶激酶(MEK)可消除p-ERK1/2、巢蛋白、GFAP和NeuN的表达。因此,ERK1/2通路可能有助于CT1刺激的hUCB-MSCs神经分化。