Cosgrove D, Gray D, Dierich A, Kaufman J, Lemeur M, Benoist C, Mathis D
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire de Génie Génétique de l'INSERM, Faculté de Médecine, Strasbourg, France.
Cell. 1991 Sep 6;66(5):1051-66. doi: 10.1016/0092-8674(91)90448-8.
We have produced mice that lack major histocompatibility complex class II antigens, permitting us to evaluate the role of these molecules in diverse aspects of T and B cell differentiation. The mutant mice show near-complete elimination of CD4+ T lymphocytes from the spleen and lymph nodes; the few remaining CD4-positive cells are preferentially localized to B cell follicles. Surprisingly, substantial numbers of CD4 single-positive cells reside in the thymus; however, these are not mature thymocytes as we currently recognize them. B lymphocytes occur in normal numbers and are capable of terminal differentiation to plasma cells. Nevertheless, several aberrations in the B cell compartment are demonstrable: a lack of germinal centers, fewer IgM+IgD+ cells in certain individuals, reduced production of serum IgG1, and complete inability to respond to T-dependent antigens. In short, the class II-negative mice have confirmed some old ideas about lymphocyte differentiation, but have provided some surprises.
我们培育出了缺乏主要组织相容性复合体II类抗原的小鼠,这使我们能够评估这些分子在T细胞和B细胞分化的各个方面所起的作用。突变小鼠的脾脏和淋巴结中CD4+ T淋巴细胞几乎完全消失;少数残留的CD4阳性细胞优先定位于B细胞滤泡。令人惊讶的是,大量CD4单阳性细胞存在于胸腺中;然而,这些并非我们目前所认识的成熟胸腺细胞。B淋巴细胞数量正常,并且能够终末分化为浆细胞。尽管如此,B细胞区室仍存在一些异常:缺乏生发中心,某些个体中IgM+IgD+细胞减少,血清IgG1产生减少,并且完全无法对T细胞依赖性抗原作出反应。简而言之,II类阴性小鼠证实了一些关于淋巴细胞分化的旧观念,但也带来了一些惊喜。