Kamada S, Shimono A, Shinto Y, Tsujimura T, Takahashi T, Noda T, Kitamura Y, Kondoh H, Tsujimoto Y
Department of Medical Genetics, Biomedical Research Center, Osaka University Medical School, Yamadaoka, Japan.
Cancer Res. 1995 Jan 15;55(2):354-9.
Transgenic mice homozygously lacking in the bcl-2 gene were generated using homologous recombination in embryonal stem cells. The complete absence of Bcl-2 alpha and -beta proteins did not interfere with normal embryonic development. Abnormalities became evident after birth, although the severity varied among homozygous null mice, bcl-2-/- mice displayed pleiotropic abnormalities similar to those in the previously described bcl-2-/- mice, including growth retardation, smaller ears, short lives, polycystic kidney, atrophic thymus and spleen with accelerated apoptotic cell death of lymphocytes, and hair hypopigmentation in the second hair follicle cycle. Our bcl-2-/- mice also revealed novel defects in the small intestine, characterized by retarded development, accelerated exfoliation of epithelial cells, and very few mitotic progenitor cells.
利用胚胎干细胞中的同源重组技术,培育出了bcl - 2基因纯合缺失的转基因小鼠。Bcl - 2α和 - β蛋白的完全缺失并不影响正常的胚胎发育。出生后异常情况变得明显,尽管纯合缺失小鼠的严重程度有所不同,但bcl - 2 - / - 小鼠表现出与先前描述的bcl - 2 - / - 小鼠相似的多效性异常,包括生长迟缓、耳朵较小、寿命短、多囊肾、胸腺和脾脏萎缩以及淋巴细胞凋亡加速导致的细胞死亡,并且在第二个毛囊周期出现毛发色素减退。我们的bcl - 2 - / - 小鼠在小肠中还发现了新的缺陷,其特征为发育迟缓、上皮细胞脱落加速以及有丝分裂祖细胞极少。