Havasi Parvaneh, Soleimani Masoud, Morovvati Hassan, Bakhshandeh Behnaz, Nabiuni Mohammad
Department of developmental biology, faculty of biological science, Kharazmi University, Tehran, Iran ; Stem Cell Biology Department, Stem Cell Technology Research Center, Tehran, Iran.
Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Basic Clin Neurosci. 2014 Spring;5(2):117-23.
The native inability of nervous system to regenerate, encourage researchers to consider neural tissue engineering as a potential treatment for spinal cord injuries. Considering the suitable characteristics of induced pluripotent stem cells (iPSCs) for tissue regeneration applications, in this study we investigated the adhesion, viability and proliferation of neural progenitors (derived from human iPSCs) on aligned poly-caprolactone (PCL) nanofibers.
Aligned poly-caprolactone nanofibrous scaffold was fabricated by electrospinning and characterized by scanning electron microscopy (SEM). Through neural induction, neural progenitor cells were derived from induced pluripotent stem cells. After cell seeding on the scaffolds, their proliferation was investigated on different days of culture.
According to the SEM micrographs, the electrospun PCL scaffolds were aligned along with uniformed morphology. Evaluation of adhesion and viability of neural progenitor cells on plate (control) and PCL scaffold illustrated increasing trends in proliferation but this rate was higher in scaffold group. The statistical analyses confirmed significant differences between groups on 36h and 48h.
Evaluation of cell proliferation along with morphological assessments, staining and SEM finding suggested biocompatibility of the PCL scaffolds and suitability of the combination of the mentioned scaffold and human iPS cells for neural regeneration.
神经系统自身无法再生,这促使研究人员将神经组织工程视为脊髓损伤的一种潜在治疗方法。鉴于诱导多能干细胞(iPSC)在组织再生应用中的合适特性,在本研究中,我们研究了神经祖细胞(源自人iPSC)在排列的聚己内酯(PCL)纳米纤维上的黏附、活力和增殖情况。
通过静电纺丝制备排列的聚己内酯纳米纤维支架,并通过扫描电子显微镜(SEM)进行表征。通过神经诱导,从诱导多能干细胞中获得神经祖细胞。将细胞接种到支架上后,在不同培养天数研究其增殖情况。
根据SEM显微照片,静电纺丝的PCL支架排列整齐,形态均匀。对神经祖细胞在平板(对照)和PCL支架上的黏附及活力评估表明,增殖呈上升趋势,但支架组的增殖率更高。统计分析证实,两组在36小时和48小时时存在显著差异。
对细胞增殖的评估以及形态学评估、染色和SEM结果表明,PCL支架具有生物相容性,且上述支架与人iPS细胞的组合适用于神经再生。