人白细胞干扰素制剂在白细胞条件培养基中对人造血干细胞具有刺激活性的干扰。

L Kanz, G W Löhr, A A Fauser
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引用次数: 0

摘要

在植物血凝素(PHA-LCM)存在的情况下,白细胞调节的培养基促进来自人骨髓的多系造血祖细胞的生长。然而,在人白细胞干扰素制剂存在下制备的PHA-LCM不支持混合集落形成。通过凝胶过滤、亲和层析和凝胶电泳对PHA-LCM粗制物进行表征。无干扰素制备的PHA-LCM在Sephacryl S-300上的洗脱谱显示出明显的峰值,刺激了多能干细胞(cfu -gem)和承诺前体(CFU-c, BFU-e)的生长。用1000 U/ml干扰素制备的PHA-LCM凝胶过滤,发现洗脱剖面发生了变化。洗脱后的物质无促生长活性。我们得出结论,用人白细胞干扰素制备的PHA-LCM的刺激活性被取消,可能是由于刺激分子的产生减少,这表明干扰素干扰了既定和非既定造血祖细胞集落形成所需的分子事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interference of a human leukocyte interferon preparation with stimulatory activities in leukocyte-conditioned medium for human hematopoietic stem cells.

Medium conditioned by leukocytes in the presence of phytohemagglutinin (PHA-LCM) promotes the growth of multilineage hemopoietic progenitors derived from human bone marrow. However, PHA-LCM prepared in the presence of a human leukocyte interferon preparation does not support mixed colony formation. Crude PHA-LCM preparations were characterized by gel filtration, affinity chromatography, and gel electrophoresis. The elution profile on Sephacryl S-300 of PHA-LCM prepared without interferon showed a distinct peak that stimulated the growth of pluripotent stem cells (CFU-gemm) and committed precursors (CFU-c, BFU-e). Gel filtration of PHA-LCM, prepared with 1000 U/ml of interferon, revealed a change in the elution profile. The eluted material demonstrated no growth-promoting activities. We conclude that the abolished stimulatory activity of PHA-LCM, prepared with human leukocyte interferon, might be due to a reduced production of stimulatory molecules, suggesting that interferon interferes with the molecular events required for colony formation of committed and noncommitted hemopoietic progenitors.

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