Title of article
Differentiation of Human Pluripotent Stem Cells into Mesodermal and Ectodermal Derivatives Is Independent of the Type of Isogenic Reprogrammed Somatic Cells
Author/Authors
Philonenko, E.S. Vavilov Institute of General Genetics - Russian Academy of Sciences, russia , Shutova, M.V. Vavilov Institute of General Genetics - Russian Academy of Sciences, russia , Khomyakova, Е.А. Vavilov Institute of General Genetics - Russian Academy of Sciences, russia , Vassina, Е.М. Vavilov Institute of General Genetics - Russian Academy of Sciences, russia , Lebedeva, О.S. Vavilov Institute of General Genetics - Russian Academy of Sciences, russia , Kiselev, S.L. Vavilov Institute of General Genetics - Russian Academy of Sciences, russia , Lagarkova, М.А Vavilov Institute of General Genetics - Russian Academy of Sciences, russia
Pages
7
From page
68
To page
74
Abstract
Induced pluripotent stem cells (iPSCs) have the capacity to unlimitedly proliferate and differentiate into all types of somatic cells. This capacity makes them a valuable source of cells for research and clinical use. However, the type of cells to be reprogrammed, the selection of clones, and the various genetic manipulations during reprogramming may have an impact both on the properties of iPSCs and their differentiated derivatives. To assess this influence, we used isogenic lines of iPSCs obtained by reprogramming of three types of somatic cells differentiated from human embryonic stem cells. We showed that technical manipulations invitro, such as cell sorting and selection of clones, did not lead to the bottleneck effect, and that isogenic iPSCs derived from different types of somatic cells did not differ in their ability to differentiate into the hematopoietic and neural directions. Thus, the type of somatic cells used for the generation of fully reprogrammed iPSCs is not important for the practical and scientific application of iPSCs.
Farsi abstract
فاقد چكيده فارسي
Keywords
induced pluripotent stem cells , human embryonic stem cells , transcription , hematopoiesis , neurons , methylation
Journal title
Acta Naturae
Serial Year
2017
Full Text URL
Record number
2616391
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