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在由经AcSDKP处理的犬的贴壁层建立的长期骨髓培养物中造血作用受到抑制。

Inhibition of hematopoiesis in long-term marrow cultures established on adherent layers from AcSDKP-treated dogs.

作者信息

Hong D S, Graham T, Ewel C, Storb R, Deeg H J

机构信息

Transplantation Biology Program, Fred Hutchinson Cancer Research Center, Seattle, WA 98104-2092, USA.

出版信息

Exp Hematol. 1995 Jul;23(7):639-44.

PMID:7601256
Abstract

The tetrapeptide Acetyl-N-Ser-Asp-Lys-Pro (AcSDKP) interferes with G1/S phase progression in hematopoietic precursors. We investigated the effect of AcSDKP on in vitro and in vivo hematopoiesis in a canine model. AcSDKP, added daily for 2 weeks to long-term marrow culture (LTMC) at concentrations > 10(-8)M, reversibly inhibited colony-forming unit granulocyte/macrophage (CFU-GM) formation (p < 0.001 and p < 0.05 for 10(-6) and 10(-7)M, respectively). Inhibition was more profound when AcSDKP addition was begun at the initiation rather than at the time of recharging the cultures. Next, seven dogs were given AcSDKP in vivo at 50 (n = 2), 250 (n = 2), or 500 micrograms/kg/day (n = 3) via continuous infusion for 7 days. No adverse effects were observed. LTMCs were established on days -9, -2, +7, and +28 of AcSDKP. One week later (days -2, +5, +14, and +35), adherent layers were recharged with fresh autologous marrow, and CFU-GM in nonadherent cells was assayed weekly beginning 1 week after recharging. The cumulative number of CFU-GM harvested from LTMCs was dependent upon the time of initiation of LTMC. The difference between day -2 (adherent layer pre-AcSDKP; recharge on AcSDKP) and day +7 culture (adherent layer on AcSDKP; recharge after discontinuation of AcSDKP, p < 0.001) suggested an effect of AcSDKP on the adherent stromal layer. Ex vivo hematopoiesis partially recovered following discontinuation of AcSDKP, although CFU-GMs were still reduced in LTMCs established on day +28. Normal nonadherent cells recharged onto allogeneic adherent/layers obtained during AcSDKP treatment grew significantly fewer CFU-GM than cultures on adherent cells obtained before AcSDKP treatment (p < 0.05). Therefore, these data suggest that AcSDKP affects not only hematopoietic cells but also cells of the adherent layer.

摘要

四肽乙酰 - N - 丝氨酸 - 天冬氨酸 - 赖氨酸 - 脯氨酸(AcSDKP)干扰造血前体细胞的G1/S期进程。我们在犬模型中研究了AcSDKP对体外和体内造血的影响。以浓度>10^(-8)M每日向长期骨髓培养(LTMC)中添加AcSDKP 2周,可可逆性抑制集落形成单位粒细胞/巨噬细胞(CFU - GM)的形成(10^(-6)M和10^(-7)M时分别为p < 0.001和p < 0.05)。当在培养开始时而不是在补充培养物时开始添加AcSDKP,抑制作用更显著。接下来,7只犬通过连续输注7天,分别以50(n = 2)、250(n = 2)或500微克/千克/天(n = 3)的剂量在体内给予AcSDKP。未观察到不良反应。在给予AcSDKP的第 - 9、 - 2、 + 7和 + 28天建立LTMC。1周后(第 - 2、 + 5、 + 14和 + 35天),用新鲜自体骨髓补充贴壁层,并在补充后1周开始每周测定非贴壁细胞中的CFU - GM。从LTMC收获的CFU - GM的累积数量取决于LTMC开始的时间。第 - 2天(AcSDKP前的贴壁层;在AcSDKP时补充)和第 + 7天培养(AcSDKP上的贴壁层;停止AcSDKP后补充,p < 0.001)之间的差异表明AcSDKP对贴壁基质层有影响。在停止给予AcSDKP后,体外造血部分恢复,尽管在第 + 28天建立的LTMC中CFU - GM仍然减少。与在AcSDKP治疗前获得的贴壁细胞上的培养物相比,在AcSDKP治疗期间获得的同种异体贴壁层上重新接种的正常非贴壁细胞产生的CFU - GM显著减少(p < 0.05)。因此,这些数据表明AcSDKP不仅影响造血细胞,还影响贴壁层细胞。

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