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Record Nr. |
UNINA9910253944103321 |
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Titolo |
In Vivo Reprogramming in Regenerative Medicine / / edited by Açelya Yilmazer |
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Pubbl/distr/stampa |
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Cham : , : Springer International Publishing : , : Imprint : Humana, , 2017 |
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ISBN |
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Edizione |
[1st ed. 2017.] |
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Descrizione fisica |
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1 online resource (XVII, 103 p. 15 illus. in color.) |
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Collana |
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Stem Cell Biology and Regenerative Medicine, , 2196-8985 |
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Disciplina |
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Soggetti |
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Regenerative medicine |
Tissue engineering |
Stem cells |
Cell culture |
Surgical transplantation |
Regenerative Medicine/Tissue Engineering |
Stem Cells |
Cell Culture |
Transplant Surgery |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Nota di contenuto |
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Chapter 1. Introduction to in vivo cell Reprogramming Technology -- Chapter 2. In vivo Reprogramming for Regenerating Insulin-Secreting Cells -- Chapter 3. Direct Reprogramming to Beta Cells -- Chapter 4. In vivo Lineage Reprogramming of Fibroblasts to Cardiomyocytes for Heart Regeneration -- Chapter 5: In vivo cell Reprogramming for Long-term Pluripotency -- Chapter 6: In vivo Transient Reprogramming Towards Pluripotency for Tissue Repair and Regeneration -- Chapter 7. Challenges and Future Perspectives for in vivo Reprogramming Technology. |
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Sommario/riassunto |
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There have been significant improvements in the development of cell based therapies; however, current treatment strategies still suffer from some problems: the need for long in vitro culture conditions, inefficient |
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delivery of cells by scaffolds and low incorporation and grafting efficiencies. Therefore, in vivo reprogramming has emerged as a novel treatment technology. In the process of in vivo reprogramming, cells switch to another cell type within the living organism. Leaders in the field discuss how in vivo reprogramming can be used for tissue repair and regeneration in different organs, including pancreas, liver and heart. Furthermore, recent studies on in vivo cell reprogramming towards pluripotency are also reviewed. Current challenges of these preclinical studies are discussed and hypothesis and suggestions are given in order to improve the current strategies to achieve translation into clinic. . |
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