| Literature DB >> 29687742 |
Behrouz Farhadihosseinabadi1, Mehrdad Farahani1, Tahereh Tayebi1, Ameneh Jafari1,2, Felor Biniazan1, Khashayar Modaresifar3, Hamideh Moravvej4, Soheyl Bahrami5, Heinz Redl5, Lobat Tayebi6, Hassan Niknejad1.
Abstract
One of the main goals of tissue engineering and regenerative medicine is to develop skin substitutes for treating deep dermal and full thickness wounds. In this regard, both scaffold and cell source have a fundamental role to achieve exactly the same histological and physiological analog of skin. Amnion epithelial and mesenchymal cells possess the characteristics of pluripotent stem cells which have the capability to differentiate into all three germ layers and can be obtained without any ethical concern. Amniotic cells also produce different growth factors, angio-modulatory cytokines, anti-bacterial peptides and a wide range of anti-inflammatory agents which eventually cause acceleration in wound healing. In addition, amniotic membrane matrix exhibits characteristics of an ideal scaffold and skin substitute through various types of extracellular proteins such as collagens, laminins and fibronectins which serve as an anchor for cell attachment and proliferation, a bed for cell delivery and a reservoir of drugs and growth factors involved in wound healing process. Recently, isolation of amniotic cells exosomes, surface modification and cross-linking approaches, construction of amnion based nanocomposites and impregnation of amnion with nanoparticles, construction of amnion hydrogel and micronizing process promoted its properties for tissue engineering. In this manuscript, the recent progress was reviewed which approve that amnion-derived cells and matrix have potential to be involved in skin substitutes; an enriched cell containing scaffold which has a great capability to be translated into the clinic.Keywords: Amniotic membrane; epithelial stem cell; mesenchymal stem cell; nanocomposite; regenerative medicine; scaffold; tissue engineering
Mesh:
Year: 2018 PMID: 29687742 DOI: 10.1080/21691401.2018.1458730
Source DB: PubMed Journal: Artif Cells Nanomed Biotechnol ISSN: 2169-1401 Impact factor: 5.678