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2,3,7,8-四氯二苯并对二噁英对2/3部分肝切除诱导的大鼠肝细胞增殖的抑制作用。

Inhibitory effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin on rat hepatocyte proliferation induced by 2/3 partial hepatectomy.

作者信息

Bauman J W, Goldsworthy T L, Dunn C S, Fox T R

机构信息

Chemical Industry Institute of Toxicology, Research Triangle Park, NC 27709, USA.

出版信息

Cell Prolif. 1995 Aug;28(8):437-51. doi: 10.1111/j.1365-2184.1995.tb00084.x.

Abstract

To better understand the mode of action of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induced alterations in hepatic cell proliferation and the potential link to tumour-promoting activity, we investigated the effects of TCDD on the expression of certain key genes involved in liver cell growth and the effects of TCDD on induced hepatocyte cell proliferation. Gene expression analysis was conducted, by Northern blot hybridization, using RNA isolated from female Sprague-Dawley rat livers collected at various times during a 14-day dosing period with TCDD known to produce alterations in cell proliferation. No major changes were observed in the expression of the transforming growth factors TGF-alpha and TGF-beta or in oncogenes ras, src and myc. However, the expression of the transcription factors C/EBP, HNF-1 alpha and HNF-4 decreased after 14 days of TCDD treatment. To investigate how TCDD affects hepatic growth, cell proliferation analysis was conducted in rats stimulated to undergo hepatocyte proliferation following either 2/3 partial hepatectomy or lead nitrate treatment. Cell proliferation was quantified by means of immunocytochemical detection of Proliferating Cell Nuclear Antigen (PCNA). Fourteen days of pretreatment with TCDD caused an overall inhibition of hepatocytes in the growth fraction (G1, S, G2 and M) from 61 +/- 3% in the control-partial hepatectomy group to 41 +/- 3% in the TCDD-partial hepatectomy group. A periportal pattern of cell proliferation was observed in the TCDD-partial hepatectomy group as compared to the panlobular pattern of cell proliferation in the control-partial hepatectomy group. TCDD pretreatment also produced an inhibition of cell proliferation induced by the liver mitogen lead nitrate. TCDD-induced inhibition of hepatocyte proliferation could play a role in TCDD tumour promotion and hepatocarcinogenesis through the creation of a environment whereby preneoplastic cells continue to expand while normal hepatocyte proliferation is inhibited.

摘要

为了更好地理解2,3,7,8-四氯二苯并对二恶英(TCDD)诱导肝细胞增殖改变的作用模式以及与肿瘤促进活性的潜在联系,我们研究了TCDD对参与肝细胞生长的某些关键基因表达的影响以及TCDD对诱导的肝细胞增殖的影响。通过Northern印迹杂交进行基因表达分析,使用从在14天给药期内不同时间收集的雌性Sprague-Dawley大鼠肝脏中分离的RNA,已知该给药期TCDD会引起细胞增殖改变。在转化生长因子TGF-α和TGF-β或癌基因ras、src和myc的表达中未观察到重大变化。然而,TCDD处理14天后,转录因子C/EBP、HNF-1α和HNF-4的表达下降。为了研究TCDD如何影响肝脏生长,在2/3部分肝切除或硝酸铅处理后刺激大鼠进行肝细胞增殖的情况下进行细胞增殖分析。通过免疫细胞化学检测增殖细胞核抗原(PCNA)对细胞增殖进行定量。TCDD预处理14天导致生长分数(G1、S、G2和M)中的肝细胞总体抑制,从对照部分肝切除组的61±3%降至TCDD部分肝切除组的41±3%。与对照部分肝切除组的全小叶细胞增殖模式相比,在TCDD部分肝切除组中观察到门静脉周围细胞增殖模式。TCDD预处理还抑制了肝有丝分裂原硝酸铅诱导的细胞增殖。TCDD诱导的肝细胞增殖抑制可能通过创造一种环境在TCDD肿瘤促进和肝癌发生中起作用,在此环境中,癌前细胞继续扩增而正常肝细胞增殖受到抑制。

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