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质子束对早期发育的斑马鱼(Danio rerio)胚胎血管形成的影响。

Effect of proton beam on blood vessel formation in early developing zebrafish (Danio rerio) embryos.

作者信息

Jang Gun Hyuk, Ha Ji-Hong, Huh Tae-Lin, Lee You Mie

机构信息

School of Life Sciences and Biotechnology, College of Natural Sciences, Kyungpook National University, Daegu, 702-701, Korea.

出版信息

Arch Pharm Res. 2008 Jun;31(6):779-85. doi: 10.1007/s12272-001-1226-1. Epub 2008 Jun 19.

Abstract

Proton beam therapy can kill tumor cells while saving normal cells because of its specific energy delivery properties and so is used to various tumor patients. However, the effect of proton beam on angiogenesis in the development of blood vessels has not been determined. Here we used the zebrafish model to determine in vivo whether proton beam inhibits angiogenesis. Flk-1-GFP transgenic embryos irradiated with protons (35 MeV, spread out Bragg peak, SOBP) demonstrated a marked inhibition of embryonic growth and an altered fluorescent blood vessel development in the trunk region. When cells were stained with acridine orange to evaluate DNA damage, the number of green fluorescent cell death spots was increased in trunk regions of irradiated embryos compared to non-irradiated control embryos. Proton beam also significantly increased the cell death rate in human umbilical vein endothelial cells (HUVEC), but pretreatment with N-acetyl cystein (NAC), an antioxidant, reduced the proton-induced cell death rate (p<0.01). Moreover, pretreatment with NAC abrogated the inhibition of trunk vessel development and prevented the trunk malformation caused by proton irradiation. In conclusion, proton irradiation significantly inhibited in vivo vascular development possibly due to increased vascular cell death via reactive oxygen species formation.

摘要

质子束疗法因其特定的能量传递特性,在杀死肿瘤细胞的同时能保护正常细胞,因此被用于各类肿瘤患者。然而,质子束对血管生成过程中血管形成的影响尚未明确。在此,我们利用斑马鱼模型在体内确定质子束是否抑制血管生成。用质子(35兆电子伏特,扩展布拉格峰,SOBP)照射Flk-1-GFP转基因胚胎,结果显示胚胎生长受到显著抑制,并且躯干区域的荧光血管发育发生改变。当用吖啶橙对细胞进行染色以评估DNA损伤时,与未照射的对照胚胎相比,照射后胚胎躯干区域绿色荧光细胞死亡斑点的数量增加。质子束还显著提高了人脐静脉内皮细胞(HUVEC)的细胞死亡率,但用抗氧化剂N-乙酰半胱氨酸(NAC)预处理可降低质子诱导的细胞死亡率(p<0.01)。此外,NAC预处理消除了对躯干血管发育的抑制,并防止了质子照射引起的躯干畸形。总之,质子照射可能通过活性氧的形成增加血管细胞死亡,从而显著抑制体内血管发育。

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