| Literature DB >> 20533407 |
Petra Kraus1, Geraldine Leong, Valerie Tan, Xing Xing, Jie Wei Goh, Sook Peng Yap, Thomas Lufkin.
Abstract
The long-standing traditional method of delivering embryonic stem (ES) cells adjacent to the inner cell mass (ICM) of blastocysts to generate chimeras improved with the advent of laser- or Piezo assisted 8-cell embryo microinjection. Building on this technology but omitting either the laser or the Piezo to penetrate the zona pellucida and making use of earlier embryonic stages (2-cell and 4-cell), we were able to significantly speed up and economize our ES cell microinjection and chimera production throughput. We demonstrate here that embryonic (ES) and induced pluripotent stem (iPS) cells can stay fully pluripotent when delivered into 2-cell- and 4-cell-stage embryos, long before they would naturally be incorporated into the ICM of a blastocyst (E3.5) and give rise to high percentage and germline transmitting chimeras. 2010 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2010 PMID: 20533407 DOI: 10.1002/dvg.20627
Source DB: PubMed Journal: Genesis ISSN: 1526-954X Impact factor: 2.487