Hirsch E, Iglesias A, Potocnik A J, Hartmann U, Fässler R
Max Planck Institute for Biochemistry, Martinsried, Germany.
Nature. 1996 Mar 14;380(6570):171-5. doi: 10.1038/380171a0.
Adhesive interactions mediated by integrins of the beta1 subfamily are thought to be critical in controlling differentiation and migration of blood cell precursors. Here we report that chimaeric mice generated with beta1-integrin-deficient embryonic stem (ES) cells lack beta1(-/-) cells in blood and in haematopoietic organs such as spleen, thymus and bone marrow. Chimaeric embryos contain beta1-null haematopoietic cells in the yolk sac and in fetal blood but not in fetal liver. We show that such beta1(-/-) haematopoietic stem cells derived from yolk sac of 10.5-day-old chimaeric embryos readily generate erythroid and myeloid colonies and that beta1(-/-) ES cells can differentiate into mature B lymphocytes in vitro. Our results indicate that haematopoietic stem cells lacking beta1 integrins can form and differentiate into different lineages but cannot colonize the fetal liver.
由β1亚家族整合素介导的黏附相互作用被认为在控制血细胞前体的分化和迁移中起关键作用。在此我们报告,用缺乏β1整合素的胚胎干细胞(ES细胞)构建的嵌合小鼠在血液以及脾脏、胸腺和骨髓等造血器官中缺乏β1(-/-)细胞。嵌合胚胎在卵黄囊和胎儿血液中含有β1缺失的造血细胞,但在胎儿肝脏中则没有。我们发现,源自10.5天大嵌合胚胎卵黄囊的此类β1(-/-)造血干细胞很容易生成红系和髓系集落,并且β1(-/-)ES细胞在体外能够分化为成熟的B淋巴细胞。我们的结果表明,缺乏β1整合素的造血干细胞能够形成并分化为不同谱系,但无法定殖于胎儿肝脏。