Tissue Engineering And Nanotheranostics

(Steven Felgate) #1
b2815 Tissue Engineering and Nanotheranostics “9.61x6.69”

8 Tissue Engineering and Nanotheranostics

3.1. Embryonic Stem Cells


The embryonic body is the home for many stem cells that have


been shown to be pluripotent (capable of differentiation into


almost any tissue type found in the body). Their role in the devel-


opment of new organisms requires that they have a theoretically


unlimited potential for self-replication and proliferation.^36 Both of


these traits make ESCs an attractive source for tissue engineering


purposes. Theoretically, implantation of ESCs into a wound site


would provide everything necessary for complete replacement of all


damaged tissues. However, a number of significant disadvantages


are associated with this cell type. First are the ethical concerns with


the harvesting of such cells, which necessarily deprives the embry-


onic body of the ability to develop into an adult.^27 Furthermore,


due to the cells’ proliferative and pluripotent nature, the risk of


teratoma formation is high.^36 Finally, use of ESCs to form tissue


engineered constructs for allografts can result in a detrimental


immune response.^28


3.2. Induced Pluripotent Stem Cells


Recently, it was discovered that it is possible to genetically repro-


gram somatic cells to behave as pluripotent stem cells.^29 This is


conducted with genes that have been identified as essential in the


maintenance of the embryonic environment, and has been best


demonstrated on fibroblasts.^29 The benefit of this cell type, besides


the pluripotency, is the ability to use cells harvested from the


patient. The cells could be obtained from a small skin biopsy, and


would theoretically be completely compatible with the patient’s


immune system if used as an autograft. iPSCs are not without their


drawbacks, however, which include the risk of teratoma formation


and low yield of the induction process.30,31 Furthermore, the full


ramifications of genetic manipulation are not yet known.^31 Myogenic


differentiation has been accomplished through overexpression of


critical genes including Pax7 or MyoD.37,


b2815_Ch-01.indd 8 11-10-2017 06:32:16 PM

Free download pdf