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镉对前列腺干/祖细胞增殖和自我更新活性的影响。

Effects of cadmium on proliferation and self-renewal activity of prostate stem/progenitor cells.

机构信息

Faculty of Preventive Medicine, Medical College, Wuhan University of Science and Technology, Wuhan, Hubei 430065, China.

出版信息

Environ Toxicol Pharmacol. 2011 Sep;32(2):275-84. doi: 10.1016/j.etap.2011.05.015. Epub 2011 Jun 13.

Abstract

Cadmium (Cd) is an occupational and environmental pollutant that induces numerous pathological effects, including injuries to prostate. The aim of the present study was to investigate the effects of Cd on self-renewal and proliferation of prostate stem/progenitor cells (PSPC) and its possible mechanisms. Prostate epithelial cells were prepared from mice to form sphere in Matrigel/PrEGM supplemented with cadmium chloride (CdCl(2)). The data showed that CdCl(2) inhibits sphere-forming ability and proliferation of PSPC in a concentration dependent manner. Primary spheres were then passaged to form daughter spheres and we found that CdCl(2) suppressed PSPC self-renewal activity, which recovered after further passaging. We also detected the protein level of androgen receptor (AR) in the spheres of each passage. The results showed that AR in primary spheres is suppressed by CdCl(2) in a concentration dependent manner. However, no obvious change of AR was found in subsequent passages. The in vivo toxicity of CdCl(2) on PSPC was detected by giving mice drinking water with CdCl(2). Our results demonstrated in vivo inhibition effect of CdCl(2) on self-renewal activity of PSPC. Consistent with in vitro results, self-renewal activity of PSPC was recovered after CdCl(2) withdrawal. In addition, CdCl(2) also in vivo suppressed PSPC proliferation as indicated by Ki67 immunostaining. Our finding suggested that Cd may inhibit proliferation and self-renewal activity of PSPC by suppressing AR, which could be important to further understanding the complex mechanism of Cd toxicity in prostate.

摘要

镉 (Cd) 是一种职业和环境污染物,可引起许多病理效应,包括前列腺损伤。本研究旨在探讨 Cd 对前列腺干细胞/祖细胞 (PSPC) 自我更新和增殖的影响及其可能的机制。从小鼠中制备前列腺上皮细胞,在含有氯化镉 (CdCl(2)) 的 Matrigel/PrEGM 中形成球体。结果表明,CdCl(2) 以浓度依赖的方式抑制 PSPC 的球体形成能力和增殖。然后将原代球体传代形成子球体,我们发现 CdCl(2) 抑制了 PSPC 的自我更新活性,在进一步传代后得到恢复。我们还检测了每个传代球体中的雄激素受体 (AR) 蛋白水平。结果表明,CdCl(2) 以浓度依赖的方式抑制原代球体中的 AR。然而,在随后的传代中未发现 AR 明显变化。通过给予小鼠含 CdCl(2) 的饮用水来检测 CdCl(2) 对 PSPC 的体内毒性。我们的结果表明 CdCl(2) 对 PSPC 的自我更新活性具有体内抑制作用。与体外结果一致,在 CdCl(2) 去除后,PSPC 的自我更新活性得到恢复。此外,CdCl(2) 还通过抑制 AR 体内抑制 PSPC 的增殖,如 Ki67 免疫染色所示。我们的发现表明,Cd 可能通过抑制 AR 抑制 PSPC 的增殖和自我更新活性,这对于进一步了解前列腺中 Cd 毒性的复杂机制可能很重要。

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