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Survival, Proliferation, and Migration of Human Meningioma Stem-Like Cells in a Nanopeptide Scaffold Publisher



Sahab Negah S1, 2 ; Aligholi H3 ; Khaksar Z1 ; Kazemi H4 ; Modarres Mousavi SM2 ; Safahani M2, 5 ; Barati Dowom P2 ; Gorji A2, 6, 7, 8
Authors
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Authors Affiliations
  1. 1. Histology and Embryology group, Basic Science Department, Faculty of Veterinary Medicine, Shiraz University, Shiraz, Iran
  2. 2. Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran
  3. 3. Department of Neuroscience, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
  4. 4. Pediatric Department, Medical Faculty, Shahed University, Tehran, Iran
  5. 5. Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Epilepsy Research Center, Westfalische Wilhelms-Universitat Munster, Germany
  7. 7. Department of Neurology and Department of Neurosurgery, Westfalische Wilhelms-Universitat Munster, Germany
  8. 8. Department of Neuroscience, Mashhad University of Medical Sciences, Mashhad, Iran

Source: Iranian Journal of Basic Medical Sciences Published:2016


Abstract

Objective(s): In order to grow cells in a three-dimensional (3D) microenvironment, self-assembling peptides, such as PuraMatrix, have emerged with potential to mimic the extracellular matrix. The aim of the present study was to investigate the influence of the self-assembling peptide on the morphology, survival, proliferation rate, migration potential, and differentiation of human meningioma stem-like cells (hMgSCs). Materials and Methods: The efficacy of a novel method for placing hMgSCs in PuraMatrix (the injection approach) was compared to the encapsulation and surface plating methods. In addition, we designed a new method for measurement of migration distance in 3D cultivation of hMgSCs in PuraMatrix. Results: Our results revealed that hMgSCs have the ability to form spheres in stem cell culture condition. These meningioma cells expressed GFAP, CD133, vimentin, and nestin. Using the injection method, a higher proliferation rate of the hMgSCs was observed after seven days of culture. Furthermore, the novel migration assay was able to measure the migration of a single cell alone in 3D environment. Conclusion: The results indicate the injection method as an efficient technique for culturing hMgSCs in PuraMatrix. Furthermore, the novel migration assay enables us to evaluate the migration of hMgSCs. © 2016, Mashhad University of Medical Sciences. All rights reserved.
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