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      Induced Pluripotent Stem Cells in Dental and Nondental Tissue Regeneration: A Review of an Unexploited Potential

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          Abstract

          Cell-based therapies currently represent the state of art for tissue regenerative treatment approaches for various diseases and disorders. Induced pluripotent stem cells (iPSCs), reprogrammed from adult somatic cells, using vectors carrying definite transcription factors, have manifested a breakthrough in regenerative medicine, relying on their pluripotent nature and ease of generation in large amounts from various dental and nondental tissues. In addition to their potential applications in regenerative medicine and dentistry, iPSCs can also be used in disease modeling and drug testing for personalized medicine. The current review discusses various techniques for the production of iPSC-derived osteogenic and odontogenic progenitors, the therapeutic applications of iPSCs, and their regenerative potential in vivo and in vitro. Through the present review, we aim to explore the potential applications of iPSCs in dental and nondental tissue regeneration and to highlight different protocols used for the generation of different tissues and cell lines from iPSCs.

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          Most cited references145

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          Stem cells, the molecular circuitry of pluripotency and nuclear reprogramming.

          Reprogramming of somatic cells to a pluripotent embryonic stem cell-like state has been achieved by nuclear transplantation of a somatic nucleus into an enucleated egg and most recently by introducing defined transcription factors into somatic cells. Nuclear reprogramming is of great medical interest, as it has the potential to generate a source of patient-specific cells. Here, we review strategies to reprogram somatic cells to a pluripotent embryonic state and discuss our understanding of the molecular mechanisms of reprogramming based on recent insights into the regulatory circuitry of the pluripotent state.
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            Reprogramming of mouse and human cells to pluripotency using mature microRNAs.

            Induced pluripotent stem cells (iPSCs) can be generated from differentiated human and mouse somatic cells using transcription factors such as Oct4, Sox2, Klf4, and c-Myc. It is possible to augment the reprogramming process with chemical compounds, but issues related to low reprogramming efficiencies and, with a number of protocols, residual vector sequences, remain to be resolved. We show here that it is possible to reprogram mouse and human cells to pluripotency by direct transfection of mature double-stranded microRNAs (miRNAs). Our approaches use a combination of mir-200c plus mir-302 s and mir-369 s family miRNAs. Because this reprogramming method does not require vector-based gene transfer, it holds significant potential for biomedical research and regenerative medicine. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Reprogramming of human primary somatic cells by OCT4 and chemical compounds.

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                Author and article information

                Contributors
                Journal
                Stem Cells Int
                Stem Cells Int
                SCI
                Stem Cells International
                Hindawi
                1687-966X
                1687-9678
                2020
                29 March 2020
                : 2020
                : 1941629
                Affiliations
                1Oral Biology Department, Faculty of Dentistry, Cairo University, Cairo, Egypt
                2Stem Cells and Tissue Engineering Research Group, Faculty of Dentistry, Cairo University, Cairo, Egypt
                3Clinic for Conservative Dentistry and Periodontology, School of Dental Medicine, Christian Albrechts University, Kiel, Germany
                4Oral Medicine and Periodontology Department, Faculty of Dentistry, Cairo University, Cairo, Egypt
                Author notes

                Guest Editor: Alireza Moshaverinia

                Author information
                https://orcid.org/0000-0001-8262-5941
                https://orcid.org/0000-0003-2962-0070
                https://orcid.org/0000-0002-6261-3609
                Article
                10.1155/2020/1941629
                7146092
                6e0a590a-0e31-4a2e-b498-c22d286a5838
                Copyright © 2020 Israa Ahmed Radwan et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 5 December 2019
                : 6 March 2020
                Categories
                Review Article

                Molecular medicine
                Molecular medicine

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