| Literature DB >> 26858858 |
Tomoko Shofuda1, Daisuke Kanematsu2, Hayato Fukusumi2, Atsuyo Yamamoto1, Yohei Bamba3, Sumiko Yoshitatsu4, Hiroshi Suemizu5, Masato Nakamura6, Yoshikazu Sugimoto7, Miho Kusuda Furue8, Arihiro Kohara9, Wado Akamatsu3, Yohei Okada10, Hideyuki Okano3, Mami Yamasaki11, Yonehiro Kanemura12.
Abstract
Placental tissue is a biomaterial with remarkable potential for use in regenerative medicine. It has a three-layer structure derived from the fetus (amnion and chorion) and the mother (decidua), and it contains huge numbers of cells. Moreover, placental tissue can be collected without any physical danger to the donor and can be matched with a variety of HLA types. The decidua-derived mesenchymal cells (DMCs) are highly proliferative fibroblast-like cells that express a similar pattern of CD antigens as bone marrow-derived mesenchymal cells (BM-MSCs). Here we demonstrated that induced pluripotent stem (iPS) cells could be efficiently generated from DMCs by retroviral transfer of reprogramming factor genes. DMC-hiPS cells showed equivalent characteristics to human embryonic stem cells (hESCs) in colony morphology, global gene expression profile (including human pluripotent stem cell markers), DNA methylation status of the OCT3/4 and NANOG promoters, and ability to differentiate into components of the three germ layers in vitro and in vivo. The RNA expression of XIST and the methylation status of its promoter region suggested that DMC-iPSCs, when maintained undifferentiated and pluripotent, had three distinct states: (1) complete X-chromosome reactivation, (2) one inactive X-chromosome, or (3) an epigenetic aberration. Because DMCs are derived from the maternal portion of the placenta, they can be collected with the full consent of the adult donor and have considerable ethical advantages for cell banking and the subsequent generation of human iPS cells for regenerative applications.Entities:
Keywords: Decidua; Induced pluripotent stem cells (iPSCs); Mesenchymal cells; X-chromosome inactivation
Year: 2012 PMID: 26858858 PMCID: PMC4733846 DOI: 10.3727/215517912X658918
Source DB: PubMed Journal: Cell Med ISSN: 2155-1790