Tseng J, Williams M J, Lopez M R
Department of Experimental Pathology, Walter Reed Army Institute of Research, Washington, DC 20307.
Reg Immunol. 1989 Jan-Feb;2(1):50-9.
Lymphoid cells from peripheral lymph nodes, spleen, and gut-associated lymphoid tissues (mesenteric lymph nodes and Peyer's patches) of the mouse were stimulated by concanavalin A and bacterial lipopolysaccharide in culture: their migration in the mouse was studied. Lymphoblasts and small-medium lymphocytes from the cultures, irrespective of their tissue origins, showed a differential migration when they were passively transferred into syngeneic, immunoglobulin-allotype congeneic or allogeneic recipients. Large lymphoblasts, at late S and G2 + M phases and without MEL-14 reactive determinants, migrated preferentially to the gut. In contrast, small and medium lymphocytes, at Go/Gl and early S phases and with MEL-14 reaction determinants, migrated preferentially to the spleen and liver. The differential migration was shown to be an inherent characteristic of the cultured lymphoid cells. These results suggest that selective migration and lodging of lymphoid cells in the body may be determined by the phases of cell cycle and stages of differentiation.
用伴刀豆球蛋白A和细菌脂多糖在培养中刺激小鼠外周淋巴结、脾脏及肠道相关淋巴组织(肠系膜淋巴结和派伊尔结)的淋巴细胞:研究了它们在小鼠体内的迁移。培养物中的成淋巴细胞和中小淋巴细胞,不论其组织来源如何,当被被动转移到同基因、免疫球蛋白同种异型同基因或异基因受体中时,均表现出差异迁移。处于S期晚期和G2+M期且无MEL-14反应性决定簇的大型成淋巴细胞优先迁移至肠道。相反,处于G0/G1期和S期早期且有MEL-14反应性决定簇的中小淋巴细胞优先迁移至脾脏和肝脏。差异迁移被证明是培养淋巴细胞的固有特性。这些结果表明,体内淋巴细胞的选择性迁移和定位可能由细胞周期阶段和分化阶段决定。