Hatoya Shingo, Torii Ryuzo, Kondo Yasushi, Okuno Tsuyoshi, Kobayashi Kinji, Wijewardana Viskam, Kawate Noritoshi, Tamada Hiromichi, Sawada Tsutomu, Kumagai Daijiro, Sugiura Kikuya, Inaba Toshio
Department of Advanced Pathobiology, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka, Japan.
Mol Reprod Dev. 2006 Mar;73(3):298-305. doi: 10.1002/mrd.20392.
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.
胚胎干细胞(ES细胞)是具有产生任何类型细胞能力的多能细胞。在此,我们描述了从犬类囊胚中分离出类ES细胞的过程。在第一次发情的第11至16天,从比格犬母犬中收集犬类胚胎。从15只犬中总共获得了80个正常胚胎。其中,13个处于桑葚胚阶段,39个处于囊胚阶段,28个处于孵化囊胚阶段。将桑葚胚的内部或囊胚的内细胞团(ICM)进行机械分离,并培养在作为饲养层的小鼠胚胎成纤维细胞(MEF)上。在桑葚胚中,0%(0/13)形成了原代细胞集落;在囊胚中,25.6%(10/39)形成了原代细胞集落;在孵化囊胚中,67.9%(19/28)形成了原代细胞集落。这些集落通过酶解或机械分散进行分离。用胶原酶解离会导致细胞立即分化,但通过机械分散,这些细胞仍未分化,并且两个类ES细胞系(cES1、cES2)在传代8次后仍能在培养中继续生长。这些细胞具有典型的干细胞样形态,并表达碱性磷酸酶活性、阶段特异性胚胎抗原-1和Oct-4等特定标志物。这些细胞在悬浮培养中形成胚状体(EB);EB的延长培养导致形成囊性EB。当简单的EB在组织培养板上培养时,它们分化为几种类型的细胞,包括神经元样、上皮样、成纤维细胞样、黑素细胞样和心肌样细胞。这些观察结果表明,我们成功地分离并鉴定了犬类类ES细胞。