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5-氟尿嘧啶与小鼠肥大细胞前体

5-fluorouracil and mast cell precursors in mice.

作者信息

Ophir A, Berenshtein E, Ziltener H J, Razin E

机构信息

Department of Ophthalmology, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Exp Hematol. 1993 Nov;21(12):1558-62.

PMID:8405236
Abstract

In the mouse hematopoietic system, 5-fluorouracil (5-FU) reversibly inhibits the generation of multilineage colonies containing granulocyte, erythroid, megakaryocyte, and macrophage lineage. To determine the effect of 5-FU on mastopoiesis in vitro, bone marrow cells were obtained from mice, cultured, and treated with 5-FU for 14 days in an interleukin-3 (IL-3)-enriched medium. A dose-related inhibitory effect of 5-FU on mastopoiesis was found. When an inhibitory dose (1 microgram/mL) of 5-FU was supplemented to the cultures for only 2, 4, or 8 days and the cells were then recultured without the drug, we observed inhibition of mastopoiesis directly related to the time of exposure of the cells to 5-FU. To determine the effect of 5-FU on mastopoiesis in vivo, bone marrow cells from mice that had received a single intravenous (i.v.) 5-FU injection (150 mg/kg) were cultured. A virtually total absence of mast cells was noted at days 1 and 2 following 5-FU administration. A gradual reappearance of mast cells was later observed. Whether mice were injected with the drug once or with four once-daily (100 mg/kg 5-FU) injections, a similar pattern of delay of mast cell appearance was observed. The findings suggest (1) an irreversible, nonadditive, toxic effect of 5-FU on mast cell precursors and (2) that most or all of the mast cell precursors are nonquiescent cells, continuously activated or cycling. In addition, the use of 5-FU may serve as a unique model system for controlling and studying mastopoiesis in normal mice, rather than the mutated mice currently studied.

摘要

在小鼠造血系统中,5-氟尿嘧啶(5-FU)可可逆性抑制包含粒细胞、红细胞、巨核细胞和巨噬细胞系的多谱系集落生成。为了确定5-FU对体外肥大细胞生成的影响,从小鼠获取骨髓细胞,进行培养,并在富含白细胞介素-3(IL-3)的培养基中用5-FU处理14天。发现5-FU对肥大细胞生成具有剂量相关的抑制作用。当仅在培养物中添加抑制剂量(1微克/毫升)的5-FU 2天、4天或8天,然后在无药物的情况下重新培养细胞时,我们观察到肥大细胞生成的抑制与细胞接触5-FU的时间直接相关。为了确定5-FU对体内肥大细胞生成的影响,对接受单次静脉注射(i.v.)5-FU(150毫克/千克)的小鼠的骨髓细胞进行培养。在5-FU给药后的第1天和第2天,几乎完全没有肥大细胞。后来观察到肥大细胞逐渐重新出现。无论小鼠是单次注射该药物还是每天注射一次共四次(100毫克/千克5-FU),都观察到类似的肥大细胞出现延迟模式。这些发现表明:(1)5-FU对肥大细胞前体具有不可逆、非累加的毒性作用;(2)大多数或所有肥大细胞前体是非静止细胞,持续被激活或处于循环状态。此外,5-FU的使用可能作为一种独特的模型系统,用于控制和研究正常小鼠而非目前所研究的突变小鼠中的肥大细胞生成。

相似文献

1
5-fluorouracil and mast cell precursors in mice.5-氟尿嘧啶与小鼠肥大细胞前体
Exp Hematol. 1993 Nov;21(12):1558-62.
2
Interleukin-4 (IL-4) in combination with IL-11 or IL-6 reverses the inhibitory effect of IL-3 on early B lymphocyte development.白细胞介素-4(IL-4)与IL-11或IL-6联合使用可逆转IL-3对早期B淋巴细胞发育的抑制作用。
Exp Hematol. 1996 Jun;24(7):783-9.
3
5-Fluorouracil effect on cultured murine stem cell progeny and peripheral leukocytes.5-氟尿嘧啶对培养的小鼠干细胞后代及外周白细胞的影响。
Exp Hematol. 1986 Mar;14(3):207-14.
4
Restrictions in the stem cell function of murine bone marrow grafts after ex vivo expansion of short-term repopulating progenitors.短期再增殖祖细胞体外扩增后小鼠骨髓移植干细胞功能的限制
Exp Hematol. 1998 Feb;26(2):100-9.
5
[The dynamic proliferative activity of mouse bone marrow cells during the suppression and recovery of hemopoiesis after 5-fluorouracil administration to the animals].
Tsitologiia. 1993;35(10):44-51.
6
5-Fluorouracil spares hemopoietic stem cells responsible for long-term repopulation.5-氟尿嘧啶可使负责长期造血重建的造血干细胞免受损伤。
Exp Hematol. 1990 Feb;18(2):114-8.
7
The mast cell-committed progenitor. In vitro generation of committed progenitors from bone marrow.肥大细胞定向祖细胞。从骨髓中体外生成定向祖细胞。
J Immunol. 1991 Jan 1;146(1):211-6.
8
Differential effect of erythropoietin and GM-CSF on megakaryocytopoiesis from primitive bone marrow cells in serum-free conditions.促红细胞生成素和粒细胞-巨噬细胞集落刺激因子在无血清条件下对原始骨髓细胞巨核细胞生成的差异作用。
Stem Cells. 1997;15(4):286-90. doi: 10.1002/stem.150286.
9
Modulation of early B lymphopoiesis by interleukin-3.白细胞介素-3对早期B淋巴细胞生成的调节作用
Exp Hematol. 1996 Aug;24(10):1225-31.
10
Lisofylline inhibits transforming growth factor beta release and enhances trilineage hematopoietic recovery after 5-fluorouracil treatment in mice.利索茶碱可抑制转化生长因子β的释放,并促进小鼠经5-氟尿嘧啶治疗后的三系造血恢复。
Cancer Res. 1996 Jan 1;56(1):105-12.

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