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白细胞介素6在体外是人类巨核细胞的分化因子。

Interleukin 6 is a differentiation factor for human megakaryocytes in vitro.

作者信息

Kimura H, Ishibashi T, Uchida T, Maruyama Y, Friese P, Burstein S A

机构信息

1st Department of Internal Medicine, Fukushima Medical College.

出版信息

Eur J Immunol. 1990 Sep;20(9):1927-31. doi: 10.1002/eji.1830200909.

Abstract

The response of cells of the megakaryocytic lineage to interleukin 6 (IL6), a cytokine with multiple biological activities, was studied by adding the factor to human bone marrow (BM) cultures. IL6 alone had no effect on megakaryocytic colony formation in methylcellulose; however, in the presence of maximally stimulating concentrations of IL 3, almost a twofold increment in colony formation was observed. Tritiated thymidine suicide studies of BM incubated for 2 h with growth factors showed that almost one-half of megakaryocytic progenitors (CFU-Mk) preincubated with IL3 or IL3 plus IL6 were in S phase, whereas BM incubated with IL6 alone was similar to control (approximately 24% of CFU-Mk in S phase). When greater than or equal to 1 ng/ml of IL6 was added to liquid suspension cultures of BM, the size of individual megakaryocytes was significantly augmented compared with that seen in control cultures. Moreover, the DNA content of megakaryocytes grown in the presence of IL6 was increased (modal ploidy 16N) compared with cultures grown with IL3 (modal ploidy 8N). To determine if the effect of IL6 could be direct rather than mediated via accessory BM cells, the factor was added to cultures of isolated single megakaryocytes. Seventy-one percent of cells increased in diameter in the presence of IL6, while only 27% increased in size in the absence of the factor. The data show that IL6 is a direct maturation factor for human megakaryocytes, promoting increments in size and ploidy of these cells.

摘要

通过将白细胞介素6(IL6,一种具有多种生物学活性的细胞因子)添加到人骨髓(BM)培养物中,研究了巨核细胞系细胞对其的反应。单独的IL6对甲基纤维素中的巨核细胞集落形成没有影响;然而,在存在最大刺激浓度的IL3的情况下,观察到集落形成几乎增加了两倍。用生长因子孵育2小时的骨髓的氚标记胸腺嘧啶核苷自杀研究表明,预先用IL3或IL3加IL6孵育的巨核细胞祖细胞(CFU-Mk)中几乎有一半处于S期,而单独用IL6孵育的骨髓与对照相似(约24%的CFU-Mk处于S期)。当向骨髓的液体悬浮培养物中添加≥1 ng/ml的IL6时,与对照培养物相比,单个巨核细胞的大小显著增加。此外,与用IL3培养的培养物(模式倍性8N)相比,在IL6存在下生长的巨核细胞的DNA含量增加(模式倍性16N)。为了确定IL6的作用是否可能是直接的而非通过辅助性骨髓细胞介导,将该因子添加到分离的单个巨核细胞培养物中。在IL6存在的情况下,71%的细胞直径增加,而在没有该因子的情况下,只有27%的细胞大小增加。数据表明,IL6是人类巨核细胞的直接成熟因子,可促进这些细胞的大小和倍性增加。

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