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Isolation and characterization of embryonic stem‐like cells from canine blastocysts
Author(s) -
Hatoya Shingo,
Torii Ryuzo,
Kondo Yasushi,
Okuno Tsuyoshi,
Kobayashi Kinji,
Wijewardana Viskam,
Kawate Noritoshi,
Tamada Hiromichi,
Sawada Tsutomu,
Kumagai Daijiro,
Sugiura Kikuya,
Inaba Toshio
Publication year - 2006
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.20392
Subject(s) - biology , embryonic stem cell , blastocyst , embryoid body , inner cell mass , stem cell , microbiology and biotechnology , embryo , induced pluripotent stem cell , andrology , immunology , anatomy , embryogenesis , genetics , gene , medicine
Embryonic stem (ES) cells are pluripotent cells with the capacity to generate any type of cell. Here we describe the isolation of ES‐like cells from canine blastocysts. Canine embryos were collected from beagle bitches at day 11–16 of first estrus. A total of 80 normal embryos were obtained from 15 dogs. Of the embryos, 13 were at the morulae stage, 39 at the blastocyst stage, and 28 at the hatched blastocyst stage. The inside of morulae or inner cell masses (ICMs) of blastocysts were isolated mechanically, and cultured onto mouse embryonic fibroblasts (MEF) as feeder layers. Primary cell colonies were formed in 0% (0/13) of morulae, 25.6% (10/39) of blastocysts, and 67.9% (19/28) of hatched blastocysts. These colonies were separated either by enzymatic dissociation or by mechanical disaggregation. Dissociation with collagenase resulted in immediate differentiation, but with mechanical disaggregation these cells remained undifferentiated, and two ES‐like cell lines (cES1, cES2) continued to grow in culture after eight passages. These cells had typical stem cell‐like morphology and expressed specific markers such as alkaline phosphatase activity, stage specific embryonic antigen‐1 and Oct‐4. These cells formed embryoid bodies (EBs) in a suspension culture; extended culture of EBs resulted in the formation of cystic EBs. When the simple EBs were cultured on tissue culture plates, they differentiated into several types of cells including neuron‐like, epithelium‐like, fibroblast‐like, melanocyte‐like, and myocardium‐like cells. These observations indicate that we successfully isolated and characterized canine ES‐like cells. Mol. Reprod. Dev. © 2005 Wiley‐Liss, Inc.