AI Article Synopsis

  • Somatic stem cells in adults help maintain organ function but can't regenerate major cell loss, especially in limited-replicating cells like neurons and heart cells.
  • The concept of inducing pluripotency in somatic cells emerged to enhance their regenerative abilities, leading to Yamanaka's breakthrough in 2006, which identified 4 crucial genes (OCT-4, SOX-2, KLF-4, c-MYC).
  • This study reviews methods for inducing pluripotency, their differentiation applications, and the current status of induced pluripotent stem cells (iPSCs) in clinical trials, aiming to guide researchers in their clinical applications.

Article Abstract

In an adult human body, somatic stem cells are present in small amounts in almost all organs with the function of general maintenance and prevention of premature aging. But, these stem cells are not pluripotent and are unable to regenerate large cellular loss caused by infarctions or fractures especially in cells with limited replicative ability such as neurons and cardiomyocytes. These limitations gave rise to the idea of inducing pluripotency to adult somatic cells and thereby restoring their regeneration, replication and plasticity. Though many trials and research were focused on inducing pluripotency, a solid breakthrough was achieved by Yamanaka in 2006. Yamanaka's research identified 4 genes (OCT-4, SOX-2, KLF-4 and c-MYC) as the key requisite for inducing pluripotency in any somatic cells (iPSCs). Our study, reviews the major methods used for inducing pluripotency, differentiation into specific cell types and their application in both cell regeneration and disease modelling. We have also highlighted the current status of iPSCs in clinical applications by analysing the registered clinical trials. We believe that this review will assist the researchers to decide the parameters such as induction method and focus their efforts towards clinical application of iPSCs.

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Source
http://dx.doi.org/10.1007/5584_2018_173DOI Listing

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