Guillemot F P, Oliver P D, Peault B M, Le Douarin N M
J Exp Med. 1984 Dec 1;160(6):1803-19. doi: 10.1084/jem.160.6.1803.
The various cell types expressing Ia antigens in the chick and quail thymus have been studied by means of monoclonal antibodies (mAb) prepared by using chick and quail thymic adherent cells (macrophages and dendritic cells) as immunogens. Three reagents were selected by the following criteria: (a) they react with a surface determinant carried by thymic adherent cells and bursal lymphocytes, (b) they can be used to immunoprecipitate from spleen cell membrane extracts molecular entities of an apparent molecular weight close to 55,000, which can be fractionated into monomers at approximately 30,000 mol wt in dissociating conditions. Among these three reagents, two are strictly species specific, i.e., they recognize either chick (TaPl) or quail (TaCl) Ia determinants, whereas the third, TaC2, recognizes both chick and quail Ia molecules. Chimeric thymuses in which the epithelioconnective stroma is derived from the quail thymic primordium and the whole hemopoietic cell population (lymphocytes and accessory cells) are of chick origin were constructed as previously described by our group (20). The different mAb were applied on normal (quail and chick) and chimeric thymuses. It appears that the thymus is divided into two compartments in terms of the nature of cells expressing Ia: the cortex, in which class II antigens are exclusively expressed by endodermal epithelial cells, and the medulla, where the majority of nonlymphoid cells are Ia-positive cells of hemopoietic origin. A few epithelial cells only are present in the thymic medulla. They are closely intricated with the sessile Ia-positive cells, whose precursors penetrate the thymus along with the lymphocyte progenitors and which are renewed in the course of thymic development. In contrast, the epithelial reticulum, expressing Ia both in the cortex and medulla, contributes a stable thymic component. During early thymic ontogeny, the hemopoietic cells expressed detectable levels of Ia antigen before the epithelial cell network.
利用以鸡和鹌鹑胸腺贴壁细胞(巨噬细胞和树突状细胞)作为免疫原制备的单克隆抗体(mAb),对鸡和鹌鹑胸腺中表达Ia抗原的各种细胞类型进行了研究。根据以下标准选择了三种试剂:(a)它们与胸腺贴壁细胞和法氏囊淋巴细胞携带的表面决定簇发生反应;(b)它们可用于从脾细胞膜提取物中免疫沉淀表观分子量接近55,000的分子实体,在解离条件下该分子实体可被分离成约30,000摩尔重量的单体。在这三种试剂中,两种具有严格的种属特异性,即它们分别识别鸡(TaPl)或鹌鹑(TaCl)的Ia决定簇,而第三种TaC2则识别鸡和鹌鹑的Ia分子。如我们小组先前所述(20)构建了嵌合胸腺,其中上皮结缔组织基质源自鹌鹑胸腺原基,而整个造血细胞群体(淋巴细胞和辅助细胞)则来自鸡。将不同的单克隆抗体应用于正常(鹌鹑和鸡)胸腺和嵌合胸腺。就表达Ia的细胞性质而言,胸腺似乎分为两个区室:皮质,其中II类抗原仅由内胚层上皮细胞表达;髓质,其中大多数非淋巴细胞是造血来源的Ia阳性细胞。胸腺髓质中仅存在少数上皮细胞。它们与固着的Ia阳性细胞紧密交织,这些细胞的前体与淋巴细胞祖细胞一起进入胸腺,并在胸腺发育过程中更新。相比之下,在皮质和髓质中均表达Ia的上皮网状结构构成了稳定的胸腺成分。在胸腺发育早期,造血细胞在上皮细胞网络之前就表达了可检测水平的Ia抗原。