Crawford J, Cohen H J
J Cell Physiol. 1985 Aug;124(2):275-82. doi: 10.1002/jcp.1041240216.
The biochemistry of human B lymphocyte differentiation to plasma cells is incompletely understood. L-glutamine appears to be required for both lymphoblastic transformation and plasma cell formation in pokeweed-mitogen-stimulated human peripheral blood mononuclear cell cultures. Cells cultured with pokeweed mitogen in glutamine-deficient RPMI-1640 with 10% heat-inactivated and dialyzed fetal bovine serum were unable to incorporate 3H-thymidine or undergo morphologic lymphoblastic transformation assessed at 72 hours. However, 3H-thymidine incorporation could be maximally restored with as little as 0.08 mM L-glutamine or by using nondialyzed heat-inactivated fetal bovine serum, containing approximately. 1 mM L-glutamine. In subsequent cultures, using glutamine-deficient RPMI-1640 with 10% nondialyzed heat-inactivated fetal bovine serum, lymphoblastic transformation was equivalent with or without additional L-glutamine supplementation. However, only cultures with 2 mM L-glutamine supplementation underwent plasma cell differentiation as assessed by cytoplasmic staining with fluorescein-conjugated anti-immunoglobulin. When the kinetics of cellular immunoglobulin synthesis and secretion were analyzed by 3H- leucine incorporation into immunoglobulin, synthesis was 2-5 fold greater, and secretion 3-10-fold greater in cell cultures with 2 mM L-glutamine supplementation. By electron microscopy, only the glutamine-supplemented cells showed development of rough endoplasmic reticulum consistent with active immunoglobulin production. L-glutamine supplementation had no apparent effect on cell recovery, viability, % B cells, % T cells, % monocytes, or % helper and suppressor T cells. Thus, L-glutamine is essential for both lymphoblastic transformation and plasma cell differentiation. Future investigation of the selective nutritional requirements of cultured cells should yield further insights into the biochemical control of immune cell differentiation and function.
人类B淋巴细胞分化为浆细胞的生物化学过程尚未完全明了。在美洲商陆丝裂原刺激的人外周血单个核细胞培养中,L-谷氨酰胺似乎是淋巴细胞转化和浆细胞形成所必需的。在缺乏谷氨酰胺的RPMI-1640培养基中,加入10%热灭活并透析的胎牛血清培养细胞,在72小时时无法掺入3H-胸腺嘧啶核苷,也未发生形态学上的淋巴细胞转化。然而,加入低至0.08 mM的L-谷氨酰胺或使用未透析的热灭活胎牛血清(含约1 mM L-谷氨酰胺),可最大程度地恢复3H-胸腺嘧啶核苷掺入。在随后的培养中,使用缺乏谷氨酰胺的RPMI-1640培养基和10%未透析的热灭活胎牛血清,无论是否额外补充L-谷氨酰胺,淋巴细胞转化情况相当。然而,只有补充了2 mM L-谷氨酰胺的培养物通过荧光素偶联抗免疫球蛋白的细胞质染色评估发生了浆细胞分化。当通过3H-亮氨酸掺入免疫球蛋白来分析细胞免疫球蛋白合成和分泌的动力学时,在补充了2 mM L-谷氨酰胺的细胞培养物中,合成增加了2 - 5倍,分泌增加了3 - 10倍。通过电子显微镜观察,只有补充了谷氨酰胺的细胞显示出与活跃免疫球蛋白产生相一致的粗面内质网发育。补充L-谷氨酰胺对细胞回收率、活力、B细胞百分比、T细胞百分比、单核细胞百分比或辅助性和抑制性T细胞百分比没有明显影响。因此,L-谷氨酰胺对于淋巴细胞转化和浆细胞分化都是必不可少的。未来对培养细胞选择性营养需求的研究应能进一步深入了解免疫细胞分化和功能的生化控制。