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淋巴组织中生发中心与免疫记忆的关系。I. 经致敏脾白髓转移至同基因小鼠后小淋巴细胞形成的证据。

Relationship of germinal centers in lymphoid tissue to immunological memory. I. Evidence for the formation of small lymphocytes upon transfer of primed splenic white pulp to syngeneic mice.

作者信息

Wakefield J D, Thorbecke G J

出版信息

J Exp Med. 1968 Jul 1;128(1):153-69. doi: 10.1084/jem.128.1.153.

Abstract

The fate, proliferation, and developmental potentialities of cell suspensions made from white pulp containing large germinal centers have been studied in the mouse by transfer of cells labeled with thymidine-(3)H to lethally irradiated, syngeneic recipients. Radioautographic analyses were made using both smears and sections of a variety of tissues. Thymidine-(3)H-labeling patterns of white pulp showed that, initially, labeling occurred in a majority of blast and "intermediate cells" but in very few or no small lymphocytes. After intravenous transfer, most of the labeled cells localized in the lymphoid tissues of spleen, lymph nodes, and Peyer's patches. Few cells migrated to the thymus, lung, liver, and intestinal mucosa. Both after intravenous and after intraperitoneal transfer there was a rapid increase in the incidence of labeled small lymphocytes and a decrease of labeled blasts and intermediate cells. This was accompanied by an increase in the grain count of the small lymphocytes and a progressive decrease in the grain counts of the blast cells. Exposure of nonlabeled donor cells to thymidine-(3)H at various time intervals after transfer indicated that dividing cells were present early after transfer but that their incidence progressively decreased. Between 24 and 48 hr, very little cell division was detectable.

摘要

通过将用氚标记胸腺嘧啶核苷标记的细胞转移到经致死剂量照射的同基因受体小鼠体内,对含有大型生发中心的白髓制成的细胞悬液的命运、增殖及发育潜能进行了研究。使用多种组织的涂片和切片进行放射自显影分析。白髓的氚标记胸腺嘧啶核苷标记模式显示,最初,标记出现在大多数母细胞和“中间细胞”中,但很少或没有出现在小淋巴细胞中。静脉注射转移后,大多数标记细胞定位于脾脏、淋巴结和派伊尔结的淋巴组织中。很少有细胞迁移到胸腺、肺、肝脏和肠黏膜。静脉注射和腹腔注射转移后,标记小淋巴细胞的发生率迅速增加,标记母细胞和中间细胞的数量减少。这伴随着小淋巴细胞颗粒计数的增加和母细胞颗粒计数的逐渐减少。在转移后的不同时间间隔,将未标记的供体细胞暴露于氚标记胸腺嘧啶核苷,结果表明转移后早期存在分裂细胞,但其发生率逐渐降低。在24至48小时之间,几乎检测不到细胞分裂。

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