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1
Immunocytochemistry of apoptosis induced by bromodeoxyuridine in human leukemic HL-60 cells.溴脱氧尿苷诱导人白血病HL-60细胞凋亡的免疫细胞化学研究
Jpn J Cancer Res. 1997 Jan;88(1):44-8. doi: 10.1111/j.1349-7006.1997.tb00300.x.
2
The study of human myeloid differentiation using bromodeoxyuridine (BrdU).
J Cell Physiol. 1983 Jul;116(1):111-7. doi: 10.1002/jcp.1041160117.
3
Ultrastructural study of proliferating cells with an improved immunocytochemical detection of DNA-incorporated bromodeoxyuridine.
J Histochem Cytochem. 1995 Jan;43(1):21-9. doi: 10.1177/43.1.7822760.
4
Bromodeoxyuridine induces p53-dependent and -independent cell cycle arrests in human gastric carcinoma cell lines.溴脱氧尿苷诱导人胃癌细胞系中p53依赖性和非依赖性细胞周期停滞。
Pathobiology. 2001;69(2):77-85. doi: 10.1159/000048760.
5
Replication sites as revealed by double label immunofluorescence against proliferating cell nuclear antigen (PCNA) and bromodeoxyuridine (BrdU) in synchronized CHO cells and vincristine-induced multinucleate cells.通过对同步化的中国仓鼠卵巢(CHO)细胞和长春新碱诱导的多核细胞进行增殖细胞核抗原(PCNA)和溴脱氧尿苷(BrdU)的双重标记免疫荧光所揭示的复制位点。
Biol Cell. 1994;82(1):23-31. doi: 10.1016/0248-4900(94)90062-0.
6
In vitro bromodeoxyuridine labeling of nuclei: application to myotube hybridization.细胞核的体外溴脱氧尿苷标记:在肌管杂交中的应用。
J Histochem Cytochem. 1991 Oct;39(10):1421-6. doi: 10.1177/39.10.1940314.
7
DNA changes involved in the formation of metaphase chromosomes, as observed in mouse duodenal crypt cells stained by osmium-ammine. II. Tracing nascent DNA by bromodeoxyuridine into structures arising during the S phase.在经锇氨染色的小鼠十二指肠隐窝细胞中观察到的中期染色体形成过程中涉及的DNA变化。II. 用溴脱氧尿苷追踪新生DNA进入S期形成的结构。
Anat Rec. 1995 Aug;242(4):449-61. doi: 10.1002/ar.1092420403.
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Exposure to continuous bromodeoxyuridine (BrdU) differentially affects cell cycle progression of human breast and bladder cancer cell lines.持续暴露于溴脱氧尿苷(BrdU)对人乳腺癌和膀胱癌细胞系的细胞周期进程有不同影响。
Cell Prolif. 2004 Apr;37(2):195-206. doi: 10.1111/j.1365-2184.2004.00296.x.
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Bromodeoxyuridine enhancement of 1-beta-D-arabinofuranosylcytosine metabolic activation and toxicity in HL-60 leukemic cells.溴脱氧尿苷增强1-β-D-阿拉伯呋喃糖基胞嘧啶在HL-60白血病细胞中的代谢活化及毒性作用。
Cancer Res. 1988 Feb 1;48(3):517-21.
10
Hoechst fluorescence intensity can be used to separate viable bromodeoxyuridine-labeled cells from viable non-bromodeoxyuridine-labeled cells.Hoechst荧光强度可用于从存活的未用溴脱氧尿苷标记的细胞中分离出存活的用溴脱氧尿苷标记的细胞。
Cytometry. 2000 Oct 1;41(2):89-95. doi: 10.1002/1097-0320(20001001)41:2<89::aid-cyto2>3.0.co;2-i.

本文引用的文献

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Detection of bromodeoxyuridine (BrdU) in semi-thin sections of routine electron microscopic specimens digested with trypsin.
J Vet Med Sci. 1996 Jun;58(6):583-5. doi: 10.1292/jvms.58.583.
2
Differential induction of apoptosis in undifferentiated and differentiated HL-60 cells by DNA topoisomerase I and II inhibitors.DNA拓扑异构酶I和II抑制剂对未分化和分化的HL-60细胞凋亡的差异诱导作用。
Blood. 1993 Mar 1;81(5):1359-68.
3
The cell cycle related differences in susceptibility of HL-60 cells to apoptosis induced by various antitumor agents.HL-60细胞对各种抗肿瘤药物诱导凋亡的敏感性与细胞周期相关的差异。
Cancer Res. 1993 Jul 1;53(13):3186-92.
4
Apoptosis of human leukemic HL-60 cells induced to differentiate by phorbol ester treatment.佛波酯处理诱导人白血病HL-60细胞分化过程中的凋亡。
Leukemia. 1994 May;8(5):792-7.
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The calpain-calpastatin system is regulated differently during human neuroblastoma cell differentiation to Schwannian and neuronal cells.
FEBS Lett. 1994 Oct 24;353(3):327-31. doi: 10.1016/0014-5793(94)01075-7.
6
Monoclonal antibody to 5-bromo- and 5-iododeoxyuridine: A new reagent for detection of DNA replication.抗5-溴脱氧尿苷和5-碘脱氧尿苷单克隆抗体:一种检测DNA复制的新型试剂。
Science. 1982 Oct 29;218(4571):474-5. doi: 10.1126/science.7123245.
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Cell death: the significance of apoptosis.细胞死亡:细胞凋亡的意义
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8
Dependence of HL-60 myeloid cell differentiation on continuous and split retinoic acid exposures: precommitment memory associated with altered nuclear structure.HL-60髓样细胞分化对连续和分次视黄酸暴露的依赖性:与核结构改变相关的预承诺记忆。
J Cell Physiol. 1984 Mar;118(3):277-86. doi: 10.1002/jcp.1041180310.
9
Flow cytometric measurement of total DNA content and incorporated bromodeoxyuridine.通过流式细胞术测量总DNA含量和掺入的溴脱氧尿苷。
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5573-7. doi: 10.1073/pnas.80.18.5573.
10
5-Fluoro-2'-deoxyuridine incorporation in L1210 DNA.5-氟-2'-脱氧尿苷掺入L1210 DNA中。
J Biol Chem. 1981 Sep 10;256(17):8885-8.

溴脱氧尿苷诱导人白血病HL-60细胞凋亡的免疫细胞化学研究

Immunocytochemistry of apoptosis induced by bromodeoxyuridine in human leukemic HL-60 cells.

作者信息

Kondo K, Makita T

机构信息

Department of Veterinary Anatomy, Faculty of Agriculture, Yamaguchi University, Yoshida.

出版信息

Jpn J Cancer Res. 1997 Jan;88(1):44-8. doi: 10.1111/j.1349-7006.1997.tb00300.x.

DOI:10.1111/j.1349-7006.1997.tb00300.x
PMID:9045895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5921251/
Abstract

Various antitumor drugs which target tumor cells in the S-phase of the cell cycle induce apoptosis in HL-60 cells. The present study shows that apoptosis is inducible in HL-60 cells by continuous exposure to bromodeoxyuridine (BrdU), an S-phase specific reagent and a thymidine analogue. The localization of BrdU in the apoptotic cells was visualized with immunogold particles using an anti-BrdU monoclonal antibody. After 3 days of treatment with 20 microM BrdU, cells ceased to grow and their viability was significantly decreased. Morphologically, nuclear segmentation and cytoplasmic maturation were observed in many viable cells, and the dead cells showed typical features of apoptosis. The nuclear DNA of apoptotic cells was visualized by the immunocytochemical detection of BrdU with post-embedding immunogold staining. The condensed chromatin of the apoptotic cells was highly labeled with immunogold particles, while the nucleolus was sparsely labeled. The chromatin could be traced with BrdU-immunocytochemistry even after disappearance of the nuclear envelope. These results indicated that apoptosis in HL-60 cells was induced by incorporation of BrdU into DNA of the S-phase cells. Using BrdU-immunocytochemistry, the localization of nuclear DNA in apoptotic cells was visualized and the changes of nuclear structures were followed during the progression of apoptosis.

摘要

多种靶向细胞周期S期肿瘤细胞的抗肿瘤药物可诱导HL-60细胞凋亡。本研究表明,通过持续暴露于溴脱氧尿苷(BrdU),一种S期特异性试剂和胸腺嘧啶类似物,可在HL-60细胞中诱导凋亡。使用抗BrdU单克隆抗体,通过免疫金颗粒观察BrdU在凋亡细胞中的定位。用20μM BrdU处理3天后,细胞停止生长,其活力显著降低。形态学上,在许多活细胞中观察到核分割和细胞质成熟,死亡细胞表现出典型的凋亡特征。通过包埋后免疫金染色对BrdU进行免疫细胞化学检测,可观察到凋亡细胞的核DNA。凋亡细胞的浓缩染色质被免疫金颗粒高度标记,而核仁标记较少。即使在核膜消失后,也可通过BrdU免疫细胞化学追踪染色质。这些结果表明,BrdU掺入S期细胞的DNA中可诱导HL-60细胞凋亡。利用BrdU免疫细胞化学,可观察凋亡细胞中核DNA的定位,并在凋亡过程中追踪核结构的变化。