Rahal M D, Osmond D G
Immunology. 1981 Nov;44(3):463-72.
As part of a series of studies on bone marrow lymphocyte differentiation, I region-associated (Ia) and H-2K antigens have been quantified on small lymphocytes in mouse bone marrow and spleen, and correlated with cell renewal. Ia antigens were revealed radioautographically on some marrow small lymphocytes, the antigen density being lower than on spleen cells. Kinetic studies, combining surface rosetting and [3H]-thymidine labelling, showed that most Ia antigen-bearing lymphocytes were newly formed cells, rapidly renewed in the marrow. Ia antigens were first expressed after a post-mitotic lag period and increased in density with time. A minority of Ia antigen-bearing small lymphocytes in the marrow and a large majority of those in the spleen remained unlabelled by [3H]-thymidine, infused for 3-5 days. Some putative progenitor cells in the marrow showed surface Ia antigens of medium density. In neonatal mice the incidence and density of Ia antigens were low in the marrow and spleen, reaching adult values by 4 and 10 weeks of age, respectively. In contrast, H-2K antigens were expressed in high density on all lymphoid cells in both marrow and spleen from early postnatal life onwards. Thus, Ia antigens, but not H-2K antigens, behave as differentiation markers in the maturation of small lymphocytes produced in the bone marrow. In addition, some Ia antigen-bearing small lymphocytes in adult bone marrow are slowly renewed cells, putative long-lived immigrants from the recirculating pool.
作为骨髓淋巴细胞分化系列研究的一部分,已对小鼠骨髓和脾脏中小淋巴细胞上的I区相关(Ia)抗原和H-2K抗原进行了定量,并将其与细胞更新相关联。通过放射自显影法在一些骨髓小淋巴细胞上显示出Ia抗原,其抗原密度低于脾细胞。结合表面玫瑰花结形成和[3H] - 胸腺嘧啶核苷标记的动力学研究表明,大多数带有Ia抗原的淋巴细胞是新形成的细胞,在骨髓中快速更新。Ia抗原在有丝分裂后的延迟期后首次表达,并随时间密度增加。骨髓中少数带有Ia抗原的小淋巴细胞和脾脏中大多数此类细胞在注入[3H] - 胸腺嘧啶核苷3 - 5天后仍未被标记。骨髓中的一些假定祖细胞显示出中等密度的表面Ia抗原。在新生小鼠中,骨髓和脾脏中Ia抗原的发生率和密度较低,分别在4周和10周龄时达到成年值。相比之下,从出生后早期开始,H-2K抗原在骨髓和脾脏中的所有淋巴细胞上均高密度表达。因此,Ia抗原而非H-2K抗原在骨髓中产生的小淋巴细胞成熟过程中作为分化标志物。此外,成年骨髓中一些带有Ia抗原的小淋巴细胞是更新缓慢的细胞,可能是来自再循环池的长寿迁入细胞。