Abstract
It remains unclear what cells are proper for the generation of induced pluripotent stem cells (iPSCs). Leucine-rich repeat-containing G-protein coupled receptor 5 (Lgr5) is well known as a tissue stem cell and progenitor marker, both of which are reported to be sensitive to reprogramming. In the present study, we examined the reprogramming behavior of Lgr5-expressing cells (Lgr5 + cells). First, we compared reprogramming behavior using mouse Lgr5 + and Lgr5 negative (Lgr5 −) hair follicles (HFs). The number of alkaline phosphatase staining-positive cells was lesser in a well of Lgr5 + HFs than in Lgr5 − HFs; however, the ratio of Nanog + SSEA1 + cells in the cell mixture derived from Lgr5 + HFs was much higher than that from Lgr5 − HFs. Lgr5 + cells could be induced from mouse embryonic fibroblasts (MEFs) after transduction with Yamanaka factors. As shown in HFs, the progeny of Lgr5 + cells arising from MEFs highly converted into Nanog + cells and did not form Nanog − colonies. The progeny represented the status of the late reprogramming phase to a higher degree than the nonprogeny. We also confirmed this using human Lg5 + cells. Our findings suggest that the use of Lgr5 + cells will minimize sorting efforts for obtaining superior iPSCs.
Original language | English |
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Pages (from-to) | 1-9 |
Number of pages | 9 |
Journal | Stem Cell Research |
Volume | 20 |
DOIs | |
Publication status | Published - 01-04-2017 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Developmental Biology
- Cell Biology