Costa J J, Keffer J M, Goff J P, Metcalfe D D
Mast Cell Physiology Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Immunology. 1992 Jul;76(3):413-21.
Investigations of mast cell biology have often used immortalized cultured cells which are continuously proliferating. In vivo, however, only 2% or fewer tissue mast cells are actively dividing. We used aphidicolin, an inhibitor of DNA polymerase to induce a proliferative arrest of murine mast cells characterized by an inhibition of cell division and thymidine incorporation, with accumulation of cells in G1 and early S phase of the cell cycle. Uridine incorporation and cell viability were not significantly impaired. DNA synthesis and cell division both resumed rapidly upon removal of the drug. Morphometric analysis demonstrated that cell size, granule size, and number of granules per cell were all increased in aphidicolin-treated cells. Proliferative arrest also produced a 14-fold increase in cellular histamine content, but did not alter the proteoglycans synthesized by the cell. The level of c-myc mRNA was reduced in aphidicolin-arrested cells, but returned to the level observed in untreated cells within 1 hr of removal of the drug. In contrast, the constitutive steady-state RNA levels of tumour necrosis factor-alpha (TNF-alpha), B2-microglobulin, actin, and the c-Ha-ras and c-fes protooncogenes were not altered. Aphidicolin-induced proliferative arrest did not prevent the induction of TNF-alpha, interleukin-6 (IL-6) and c-fos genes in response to calcium ionophore. Both the magnitude and induction kinetics of these messages were similar in aphidicolin-treated and untreated cells. We conclude that proliferative arrest results in morphological and biochemical changes suggestive of cellular maturation, but inhibition of cell division alone is not sufficient to alter mast cell phenotype. Although optimal c-myc expression appears to require active proliferation, cytokine gene induction can occur in non-dividing cells. These data suggest that the proliferative quiescence of in vivo mast cells should not preclude their involvement in biological events via elaboration of multi-functional cytokines.
肥大细胞生物学的研究常常使用持续增殖的永生化培养细胞。然而,在体内,仅有2%或更少的组织肥大细胞处于活跃分裂状态。我们使用了阿非迪霉素,一种DNA聚合酶抑制剂,来诱导小鼠肥大细胞的增殖停滞,其特征为细胞分裂和胸苷掺入受到抑制,细胞在细胞周期的G1期和S期早期积累。尿苷掺入和细胞活力未受到显著损害。去除药物后,DNA合成和细胞分裂均迅速恢复。形态计量分析表明,经阿非迪霉素处理的细胞中,细胞大小、颗粒大小以及每个细胞的颗粒数量均增加。增殖停滞还使细胞组胺含量增加了14倍,但未改变细胞合成的蛋白聚糖。在阿非迪霉素停滞的细胞中,c-myc mRNA水平降低,但在去除药物后1小时内恢复到未处理细胞中观察到的水平。相比之下,肿瘤坏死因子-α(TNF-α)、β2-微球蛋白、肌动蛋白以及c-Ha-ras和c-fes原癌基因的组成型稳态RNA水平未发生改变。阿非迪霉素诱导的增殖停滞并未阻止肥大细胞对钙离子载体刺激产生TNF-α、白细胞介素-6(IL-6)和c-fos基因的诱导。在经阿非迪霉素处理和未处理的细胞中,这些信息的诱导幅度和动力学均相似。我们得出结论,增殖停滞导致形态和生化变化,提示细胞成熟,但仅抑制细胞分裂不足以改变肥大细胞表型。尽管最佳的c-myc表达似乎需要活跃增殖,但细胞因子基因诱导可在非分裂细胞中发生。这些数据表明,体内肥大细胞的增殖静止不应排除它们通过分泌多功能细胞因子参与生物学事件。